Post job

Patent Attorney jobs at Merck - 20 jobs

  • Patent Agent

    Bristol Myers Squibb 4.6company rating

    San Diego, CA jobs

    **Working with Us** Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . **Patent Agent - Innovation Law** **Location:** Princeton, NJ; Cambridge, MA; San Diego, CA **Position Summary:** Bristol Myers Squibb (BMS) is seeking an experienced patent agent to join our headquarters in Princeton, New Jersey, or one of our research centers in Cambridge, MA, or San Diego, CA. The patent practitioner will support clients across multiple functional areas to provide strategic advice to key stakeholders. Responsibilities will primarily include internal preparation and prosecution of patents. The patent agent will work closely with clients in various functions in a dynamic, growth-oriented environment and will collaborate with other in-house and outside attorneys to accomplish BMS objectives. **Key Responsibilities:** + Prepare and prosecute patent applications, including drafting, filing, and managing responses to office actions on a global level. + Provide strategic advice on patentability issues. + Manage patent portfolios, including conducting patent landscape analyses and developing patent strategies to protect BMS's innovations. + Manage relationships with outside counsel to ensure high-quality and cost-effective legal services. + Regularly engage with business and technical teams to provide patent-related guidance and support. + Stay updated on changes in patent requirements and regulations and ensure compliance with all relevant legal requirements. **Qualifications:** + Registered to practice before the USPTO. + 7-10 years of patent law experience in the pharmaceutical/biotechnology industry. + Bachelor's degree or equivalent in chemistry, biochemistry, or pharmaceutical sciences. An advanced degree and/or scientific research experience is preferred. + Excellent analytical, written, and verbal communication skills. + Service-oriented focus with the ability to work as part of cross-functional teams and drive results. + Highest integrity, excellent judgment, and the ability to proactively recognize and effectively assess business risk and communicate legal issues to key stakeholders. \#LI-Hybrid If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. **Compensation Overview:** Princeton - NJ - US: $163,970 - $198,687 San Diego - CA - US: $180,360 - $218,556 The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit ************************************* Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include: + **Health Coverage:** Medical, pharmacy, dental, and vision care. + **Wellbeing Support:** Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP). + **Financial Well-being and Protection:** 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support. **Work-life benefits include:** Paid Time Off + US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees) + Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown. ***Eligibility Disclosure:** T he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program. **Uniquely Interesting Work, Life-changing Careers** With a single vision as inspiring as Transforming patients' lives through science , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. **On-site Protocol** BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. **Supporting People with Disabilities** BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to ************************** . Visit careers.bms.com/ (****************************************** eeo-accessibility to access our complete Equal Employment Opportunity statement. **Candidate Rights** BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: ********************************************* **Data Protection** We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at **************************************** . Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at ******************** . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley. R1597473 : Patent Agent **Company:** Bristol-Myers Squibb **Req Number:** R1597473 **Updated:** 2026-01-21 03:20:16.967 UTC **Location:** Princeton-NJ Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.
    $180.4k-218.6k yearly Easy Apply 48d ago
  • Job icon imageJob icon image 2

    Looking for a job?

    Let Zippia find it for you.

  • Patent Agent

    Bristol Myers Squibb 4.6company rating

    Princeton, NJ jobs

    Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us. Patent Agent - Innovation Law Location: Princeton, NJ; Cambridge, MA; San Diego, CA Position Summary: Bristol Myers Squibb (BMS) is seeking an experienced patent agent to join our headquarters in Princeton, New Jersey, or one of our research centers in Cambridge, MA, or San Diego, CA. The patent practitioner will support clients across multiple functional areas to provide strategic advice to key stakeholders. Responsibilities will primarily include internal preparation and prosecution of patents. The patent agent will work closely with clients in various functions in a dynamic, growth-oriented environment and will collaborate with other in-house and outside attorneys to accomplish BMS objectives. Key Responsibilities: Prepare and prosecute patent applications, including drafting, filing, and managing responses to office actions on a global level. Provide strategic advice on patentability issues. Manage patent portfolios, including conducting patent landscape analyses and developing patent strategies to protect BMS's innovations. Manage relationships with outside counsel to ensure high-quality and cost-effective legal services. Regularly engage with business and technical teams to provide patent-related guidance and support. Stay updated on changes in patent requirements and regulations and ensure compliance with all relevant legal requirements. Qualifications: Registered to practice before the USPTO. 7-10 years of patent law experience in the pharmaceutical/biotechnology industry. Bachelor's degree or equivalent in chemistry, biochemistry, or pharmaceutical sciences. An advanced degree and/or scientific research experience is preferred. Excellent analytical, written, and verbal communication skills. Service-oriented focus with the ability to work as part of cross-functional teams and drive results. Highest integrity, excellent judgment, and the ability to proactively recognize and effectively assess business risk and communicate legal issues to key stakeholders. #LI-Hybrid If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Compensation Overview: Princeton - NJ - US: $163,970 - $198,687 San Diego - CA - US: $180,360 - $218,556 The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit ************************************* Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include: Health Coverage: Medical, pharmacy, dental, and vision care. Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP). Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support. Work-life benefits include: Paid Time Off US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees) Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown. *Eligibility Disclosure: The summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients' lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. Supporting People with Disabilities BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to **************************. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement. Candidate Rights BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: ********************************************* Data Protection We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at ***************************************** Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at ********************. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley. R1597473 : Patent Agent
    $180.4k-218.6k yearly Auto-Apply 49d ago
  • Patent Agent

    Bristol Myers Squibb 4.6company rating

    Princeton, NJ jobs

    **Working with Us** Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . **Patent Agent - Innovation Law** **Location:** Princeton, NJ; Cambridge, MA; San Diego, CA **Position Summary:** Bristol Myers Squibb (BMS) is seeking an experienced patent agent to join our headquarters in Princeton, New Jersey, or one of our research centers in Cambridge, MA, or San Diego, CA. The patent practitioner will support clients across multiple functional areas to provide strategic advice to key stakeholders. Responsibilities will primarily include internal preparation and prosecution of patents. The patent agent will work closely with clients in various functions in a dynamic, growth-oriented environment and will collaborate with other in-house and outside attorneys to accomplish BMS objectives. **Key Responsibilities:** + Prepare and prosecute patent applications, including drafting, filing, and managing responses to office actions on a global level. + Provide strategic advice on patentability issues. + Manage patent portfolios, including conducting patent landscape analyses and developing patent strategies to protect BMS's innovations. + Manage relationships with outside counsel to ensure high-quality and cost-effective legal services. + Regularly engage with business and technical teams to provide patent-related guidance and support. + Stay updated on changes in patent requirements and regulations and ensure compliance with all relevant legal requirements. **Qualifications:** + Registered to practice before the USPTO. + 7-10 years of patent law experience in the pharmaceutical/biotechnology industry. + Bachelor's degree or equivalent in chemistry, biochemistry, or pharmaceutical sciences. An advanced degree and/or scientific research experience is preferred. + Excellent analytical, written, and verbal communication skills. + Service-oriented focus with the ability to work as part of cross-functional teams and drive results. + Highest integrity, excellent judgment, and the ability to proactively recognize and effectively assess business risk and communicate legal issues to key stakeholders. \#LI-Hybrid If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. **Compensation Overview:** Princeton - NJ - US: $163,970 - $198,687 San Diego - CA - US: $180,360 - $218,556 The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit ************************************* Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include: + **Health Coverage:** Medical, pharmacy, dental, and vision care. + **Wellbeing Support:** Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP). + **Financial Well-being and Protection:** 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support. **Work-life benefits include:** Paid Time Off + US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees) + Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown. ***Eligibility Disclosure:** T he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program. **Uniquely Interesting Work, Life-changing Careers** With a single vision as inspiring as Transforming patients' lives through science , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. **On-site Protocol** BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. **Supporting People with Disabilities** BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to ************************** . Visit careers.bms.com/ (****************************************** eeo-accessibility to access our complete Equal Employment Opportunity statement. **Candidate Rights** BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: ********************************************* **Data Protection** We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at **************************************** . Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at ******************** . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley. R1597473 : Patent Agent **Company:** Bristol-Myers Squibb **Req Number:** R1597473 **Updated:** 2026-01-21 03:20:16.967 UTC **Location:** Princeton-NJ Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.
    $180.4k-218.6k yearly Easy Apply 48d ago
  • Senior Patent Agent

    Ideaya Biosciences 4.6company rating

    Remote

    Non-Solicitation Policy and Notice to Agencies and Recruiters: IDEAYA's Non-Solicitation Policy strictly prohibits agencies and recruiters from any contact and communication with IDEAYA employees, managers, and leaders to submit unsolicited candidate resumes and/or to solicit business partnerships. Submission of unsolicited candidate resumes by agencies or recruiters with or without a contract in place with IDEAYA Biosciences Inc. will not create any implied obligation. Failure to comply with this policy will result in disqualification from current and future business opportunities with IDEAYA Biosciences. All recruiting and talent agency decisions are strictly managed by the internal IDEAYA Human Resources function. All communication by external agencies and recruiters must be directed to ****************************. We ask that you only email your interest once. Job Summary About IDEAYA Biosciences: IDEAYA is a precision medicine oncology company committed to the discovery, development, and commercialization of transformative therapies for cancer. Our approach integrates expertise in small-molecule drug discovery, structural biology and bioinformatics with robust internal capabilities in identifying and validating translational biomarkers to develop tailored, potentially first-in-class targeted therapies aligned to the genetic drivers of disease. We have built a deep pipeline of product candidates focused on synthetic lethality and antibody-drug conjugates, or ADCs, for molecularly defined solid tumor indications. Our mission is to bring forth the next wave of precision oncology therapies that are more selective, more effective, and deeply personalized with the goal of altering the course of disease and improving clinical outcomes for patients with cancer. When you're at IDEAYA, you will be in the midst of brilliant minds working on precision medicine therapies to help cancer patients. We are passionate and committed about being on the forefront of oncology medicine, which means we all have a high internal drive that is at the very core of every person at IDEAYA. We are inquisitive, ask deep questions, and are data-driven innovators who like to collaborate and use team work to move science forward. For more information, please see ****************** Location: South San Francisco Position Summary: IDEAYA Biosciences is seeking an experienced Senior Patent Agent. Reporting directly to the Vice President of Intellectual Property, this role will support the Company's intellectual property function to protect the Company's small molecule product candidates. The ideal candidate will enjoy working collaboratively with inventors across various departments, senior scientific leaders, and the legal team. This position is based in our South San Francisco headquarter offices and required to be onsite four days per week per our company policy. Job Description What you'll do: Global IP portfolio management including preparing and prosecuting patent applications focusing on small molecules Partner with cross department teams to develop a deep understanding of project technology, identify patentable inventions through regular interactions with project teams, and implement IP protection strategies Identify and evaluate a range of complex risks (e.g., patentability, infringement, validity) and crafting innovative business-oriented mitigation strategies Conduct freedom to operate reviews, analyze third-party patent positions, and guide IP strategy Maintaining strong knowledge of patent case law, rules and regulations before the U.S. Patent & Trademark Office as well as other jurisdictional IP offices Manage outside legal counsel and ensure compliance with global IP laws and regulations Monitor and analyze competitive IP landscape and IP trends to assess risk and opportunities Engage in clear communication, both oral and written, to all levels of the organization with a willingness to listen and learn from others Assist in managing IP department's administration, infrastructure and policies Conduct IP diligence and provide other IP support for business development opportunities Requirements: Ph.D. in Chemistry, preferably Organic Chemistry, or Master's in Organic Chemistry Registered before the United States Patent and Trademark Office 7+ years of patent agent experience in pharmaceutical small molecules (patent preparation and prosecution), including preferably 2-3 years in-house experience Proven track record developing and implementing patent strategies with demonstrated success securing meaningful patent protection for products and related technology Excels at working independently and proactively with minimal direction, has strong organizational skills, and the ability to prioritize and balance competing projects and responsibilities Must have strong analytical skills and the ability to interpret complex scientific and legal information Proficiency in using scientific and IP databases Must have excellent written and verbal communication skills and attention to detail Total Rewards Along with our inspiring mission, and highly collaborative and inclusive environment, IDEAYA offers a competitive total rewards package that reflects our pay-for-performance philosophy where employees are eligible to be considered for merit-based salary increases, company discretionary short-term incentive plan participation, and company discretionary stock option awards (based on board approval). Our comprehensive benefits package includes, but is not limited to, medical/dental/vision coverage (100% company paid for employees and 90% company paid for dependents), 401k, ESPP, and wellness programs. The expected salary range for the role of Senior Patent Agent is $187,000 - $231,000. The final salary offered to a successful candidate will depend on several factors that may include but are not limited to the office location where this open position is located, the final candidates' experience within their profession, experience in the disease areas we are striving to make an impact in as a company, length of time within the industry, educational background, and performance during the interview process. The Company complies with all laws respecting equal employment opportunities and does not discriminate against applicants with regard to any protected characteristic as defined by federal, state, and local law. This position requires you to work onsite in the office at the Company's facilities for training & meetings, with work-from-home flexibility, and the Company requires that all employees working in its facilities be fully vaccinated (except as required by applicable law). Therefore, this position requires you to be fully vaccinated from COVID-19, subject to reasonable accommodations for medical or religious reasons, and/or as otherwise required by applicable law. The Company considers you fully vaccinated once 14 days have passed since you received either the second dose in a two-dose COVID-19 vaccine series or a single-dose COVID-19 vaccine. The vaccine must have been FDA approved, have emergency use authorization from the FDA, or, for persons fully vaccinated outside of the U.S., be listed for emergency use by the World Health Organization. IDEAYA is an equal opportunity employer. In accordance with applicable law, IDEAYA does not discriminate in hiring or otherwise in employment based on race, color, religion, sex, national origin, age, marital or veteran status, disability, sexual orientation, or any other legally protected status. EOE/AA/Vets.
    $51k-99k yearly est. Auto-Apply 60d+ ago
  • Associate Talent Partner (HRBP) - Contractor

    Fyllo 4.1company rating

    Remote

    The Associate Talent Partner plays a critical role in supporting and advising leaders within our Clinical organization. Acting as a trusted partner, this role provides employee relations support, ensures compliance with labor laws, and collaborates with key stakeholders to develop proactive people strategies. The Associate Talent Partner works closely with people leaders to foster an inclusive and high-performing workplace.Job Responsibilities: Serve as a primary point of contact for leaders within the Clinical organization, including coaching and partnering with people managers on people-related matters. Provide employee relations support, assisting employees and leaders in resolving workplace concerns while ensuring fair, consistent, and legally compliant practices. Conduct timely, objective, and thorough internal investigations, maintaining accurate documentation and detailed records. Act as a subject matter expert on work-related issues, including performance management, workplace concerns, reasonable accommodations (ADA), wage and hour compliance, complex labor law matters, and involuntary terminations. Build and maintain collaborative relationships with internal partners, including Talent Partners, HR Operations, Compliance, Talent Acquisition, Talent Development, and Legal. Develop and implement proactive strategies, programs, and policies to enhance employee engagement and organizational effectiveness. Qualifications: 2+ years of experience in employee relations, HR business partnering, or a similar HR role. Strong understanding of employment laws and HR best practices. Experience conducting employee investigations and managing workplace conflict. Ability to build trust and influence leaders at all levels of the organization. Excellent problem-solving, communication, and interpersonal skills. Strong attention to detail and ability to handle sensitive situations with discretion. Preferred Qualifications: Bachelor's degree in Human Resources, Business Administration, or a related field preferred. Experience in a healthcare organization and directly supporting Clinical Teams (MD's, Psychiatrists, Psychologists, MFT, NP's) and leaders in a Clinical setting (hospital, health system, virtual care delivery company, etc). The United States hourly range for this full time, contract position is $60.00/hour - $65.00/hour. Below is additional information on Included Health's commitment to maintaining transparent and equitable compensation practices across our distinct geographic zones. Starting base salary for you will depend on several job-related factors, unique to each candidate, which may include education; training; skills; years and depth of experience; certifications and licensure; our needs; internal peer equity; organizational considerations; and understanding of geographic and market data. Compensation structures and ranges are tailored to each zone's unique market conditions to ensure that all employees receive fair and great compensation package based on their roles and locations. Your Recruiter can share your geographic zone upon inquiry. Benefits & Perks: Your recruiter will share more about the salary range and benefits package for your role during the hiring process. About Included Health: Included Health is a new kind of healthcare company, delivering integrated virtual care and navigation. We're on a mission to raise the standard of healthcare for everyone. We break down barriers to provide high-quality care for every person in every community - no matter where they are in their health journey or what type of care they need, from acute to chronic, behavioral to physical. We offer our members care guidance, advocacy, and access to personalized virtual and in-person care for everyday and urgent care, primary care, behavioral health, and specialty care. It's all included. Learn more at includedhealth.com. ----- Included Health is an Equal Opportunity Employer and considers applicants for employment without regard to race, color, religion, sex, orientation, national origin, age, disability, genetics or any other basis forbidden under federal, state, or local law. Included Health considers all qualified applicants with arrest or conviction records in accordance with the San Francisco Fair Chance Ordinance, the Los Angeles County Fair Chance Ordinance, and California law.
    $60-65 hourly Auto-Apply 36d ago
  • Legal Manager Assets & Brands, Oncology M/W

    Ipsen 4.9company rating

    Paris, TX jobs

    Title: Legal Manager Assets & Brands, Oncology M/W Company: Ipsen Pharma (SAS) Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology, Rare Disease and Neuroscience. Supported by nearly 100 years of development experience, with global hubs in the U.S., France and the U.K, we tackle areas of high unmet medical need through research and innovation. Our passionate teams in more than 40 countries are focused on what matters and endeavor every day to bring medicines to patients in 88 countries. We build a workplace that champions human-centric leadership and fosters a culture of collaboration, excellence and impact. At Ipsen, every individual is empowered to be their true selves, grow and thrive alongside the company's success. Join us on our journey towards sustainable growth, creating real impact on patients and society! For more information, visit us at ********************** and follow our latest news on LinkedIn and Instagram. Job Description: The Legal Manager, Assets & Brands Oncology is responsible for delivering strategic legal advice and services across the full lifecycle of Ipsen's oncology portfolio. Acting as a trusted legal partner to global teams in Medical, R&D, and Product Strategy, the role supports innovation while ensuring legal and regulatory compliance. This position plays a key role in enabling business objectives through proactive risk management, contract negotiation, and cross-functional collaboration within the Global Legal Team and other corporate functions. Key Responsibilities * Provide proactive, strategic legal advice and serve as the legal business partner to global oncology teams, act as legal asset lead for designated oncology assets. * Review, analyse, and keep current on legal developments affecting the pharmaceutical industry and prevailing best practices, especially in oncology. * Ensure Ipsen's exposure, contractual liability, and risks are protected or mitigated while maximising business opportunities and ensuring alignment across the Legal Assets & Brands team. * Advise autonomously on a broad range of matters, including: * Clinical trials and real-world evidence studies * Research collaborations and alliance partnerships * Promotional campaigns, market access, pricing, and regulatory issues * Data protection, due diligence, and digital/IT solutions * Collaborations with institutions and healthcare partners * Draft, review, negotiate, and execute a wide variety of contractual agreements typical to the life sciences industry. * Ensure compliance with applicable laws, regulations, industry standards, and corporate policies. * Support strategic and operational plans through legal advice and implementation of practical solutions aligned with the Global Legal Director Oncology. * Escalate, manage, and intervene in disputes where required. * Develop and implement legal frameworks for new projects and manage associated risks. * Provide strategic legal advice on global projects across multiple jurisdictions. * Maintain and update contract templates and provide internal training. * Collaborate cross-functionally with colleagues in legal, ethics, procurement, finance, and regulatory teams. Profile You hold a master's degree in law and are qualified to practice as a lawyer. A master's degree in health law would be an additional asset. You are a qualified lawyer with EU and international legal experience, bringing at least five years of post-qualification experience gained within a life sciences team in a law firm or in-house in the pharmaceutical industry. You have strong technical expertise in commercial law and proven experience supporting life sciences businesses. Your profile demonstrates solid legal, regulatory, and commercial awareness of the issues impacting the sector, alongside a general understanding of Anti-Corruption, Competition Law, and Data Protection regulations. Exposure to Intellectual Property (IP) law in a pharmaceutical or biotech context would be a plus. You are fluent in English, and knowledge of French would be an advantage At Ipsen, we are dedicated to improving patients' lives through innovation in oncology and specialty care. This role offers the opportunity to influence global projects, work with a diverse international team, and contribute to Ipsen's mission of delivering transformative treatments. Nous nous engageons à créer un lieu de travail où chacun se sent écouté, valorisé et soutenu, où nous incarnons " The Real Us*". La valeur que nous accordons aux différentes perspectives et expériences motive notre engagement en faveur de l'inclusion et de l'égalité des chances. Lorsque nous intégrons des modes de pensée diversifiés, nous prenons des décisions plus réfléchies et découvrons des solutions plus innovantes. Ensemble, nous nous efforcons de mieux comprendre les communautés que nous servons. Cela signifie que nous voulons également vous aider à donner le meilleur de vous-même lorsque vous postulez à un poste chez nous. Si vous avez besoin d'aménagements ou d'aide pendant le processus de candidature, veuillez en informer l'équipe de recrutement. Ces informations seront traitées avec soin et n'auront aucune incidence sur le résultat de votre candidature. *Soyons nous-même
    $74k-118k yearly est. Auto-Apply 60d+ ago
  • Corporate Securities Attorney

    Sig 2.6company rating

    Philadelphia, PA jobs

    Susquehanna has a job opportunity available for a corporate attorney to join our in-house counsel / legal team in our Bala Cynwyd headquarters. In this role, you will gain tremendous insight into our business while counseling and advising business units on a broad array of legal issues. Our legal team performs an active and important role in information technology, corporate and securities transactions, venture capital and private equity deals, trading relationships (clearing agreements, ISDAs, MSLAs, etc.), and general business matters. Your role will be that of a liaison, strategizing with colleagues and business management teams on a comprehensive array of issues that are as diverse and multifaceted as our continually evolving business. In this role, you will Provide frontline legal support to various business units within Susquehanna Document, review, negotiate, and oversee corporate transactions Be trained to review and negotiate clearing, trading, financing, brokerage, and derivative agreements Document and negotiate employment agreements Review and negotiate technology license and purchasing agreements Oversee and coordinate outside counsel on an ad hoc basis What we're looking for Minimum of 4-5 years of corporate/securities related legal experience required, experience with securities trading documentation a plus Must possess strong negotiation skills Strong organization, effective planning, problem solving, and analytical skills required Superior communication skills, both oral and written, and the ability to liaise comfortably with all levels of management and outside counsel Must exhibit initiative in obtaining information needed to proceed with projects and accomplish tasks with minimal supervision Ability to be flexible and adapt to changing situations or urgent requests that may arise with little or no notice Must possess discretion and sensitivity when working with confidential information and safeguard such information appropriately Ability to exhibit independent judgment when evaluating projects or assignment needs Knowledge of Microsoft products (Excel, Word, and Outlook) Willingness to work additional and flexible hours on occasion Visa sponsorship for work authorization is not available for this position now or in the future About Susquehanna Susquehanna is a global quantitative trading firm powered by scientific rigor, curiosity, and innovation. Our culture is intellectually driven and highly collaborative, bringing together researchers, engineers, and traders to design and deploy impactful strategies in our systematic trading environment. To meet the unique challenges of global markets, Susquehanna applies machine learning and advanced quantitative research to vast datasets in order to uncover actionable insights and build effective strategies. By uniting deep market expertise with cutting-edge technology, we excel in solving complex problems and pushing boundaries together. If you're a recruiting agency and want to partner with us, please reach out to ******************. Any resume or referral submitted in the absence of a signed agreement will not be eligible for an agency fee. #LI-KD1 #LI-Onsite
    $97k-161k yearly est. Auto-Apply 8d ago
  • Corporate Attorney

    Medpace 4.5company rating

    Cincinnati, OH jobs

    Our Corporate Affairs department is seeking an experienced Attorney for our growing team. Corporate Affairs acts as in-house counsel for Medpace, and its domestic and international subsidiaries. Areas of legal practice include (but are not limited to) corporate governance, employment matters, global privacy, litigation and other areas as assigned. Responsibilities * Provide or arrange for legal services for enterprise-wide or entity-wide scope support and administrative functions; * Act as a point of contact for matters of global privacy, data protection and compliance; * Advise on US Securities Law, government contracting and immigration matters; * Review and draft contracts, manage third party contracting process; * Identify appropriate outside counsel and oversee/coordinate outsourced legal work; * Identify potential legal issues in operations, strategic planning, and business development activities and bring to attention of appropriate members of management, along with recommendations for how to address or resolve to minimize legal risk to the organization; * Maintain current working knowledge of applicable regulatory requirements and court decisions and advise management appropriately; * Ensure SOPs are in place to promote compliance with applicable laws and regulations; and * Focus on general corporate matters, with emphasis on compliance and global privacy. Qualifications * Juris Doctorate with 3-5 years of experience at a law firm or in-house; * Knowledge in corporate compliance and governance, contracts, collections and/or general litigation is preferred; * Experience with corporate governance and securities transactions is preferred; * Experience with US or Internal labor and employment law is preferred; * Excellent communication, negotiation, and leadership skills; and * Professional demeanor and strong work ethic. Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Cincinnati Perks * Cincinnati Campus Overview * Flexible work environment * Competitive PTO packages, starting at 20+ days * Competitive compensation and benefits package * Company-sponsored employee appreciation events * Employee health and wellness initiatives * Community involvement with local nonprofit organizations * Discounts on local sports games, fitness gyms and attractions * Modern, ecofriendly campus with an on-site fitness center * Structured career paths with opportunities for professional growth * Discounted tuition for UC online programs Awards * Named a Top Workplace in 2024 by The Cincinnati Enquirer * Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
    $81k-136k yearly est. Auto-Apply 13d ago
  • Associate Counsel, Employment & Immigration

    Abbvie 4.7company rating

    North Chicago, IL jobs

    AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at *************** Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok (******************************* . Job Description The Employment and Immigration Associate Counsel is responsible for providing U.S. employment and immigration law guidance and support to AbbVie's global pharmaceutical business. In partnership with AbbVie's employment and immigration law attorneys, this attorney will help manage AbbVie's U.S. immigration program portfolio and provide legal counsel to clients regarding employment and immigration laws. The attorney will interface with internal and outside legal counsel and stakeholders. This position reports to the VP, Employment, Immigration & Labor. This position requires the individual to work a hybrid work schedule of three days a week at the designated work site in North Chicago, IL. Core Job Responsibilities: + Manage and maintain a portfolio of U.S. business immigration matters in compliance with U.S. immigration laws and AbbVie policies. Manage relationships with AbbVie's outside counsel. + Advise and represent AbbVie on workplace employment issues including government agency charges and attorney demand letters. Prepare substantive written responses. + Provide counseling to Human Resources regarding employment and immigration matters. Communicate with internal clients regarding employment and immigration laws. + Provide legal support on AbbVie policies, agreements, compliance initiatives and projects. Qualifications + JD degree and appropriate licensure to practice law in Illinois. + Minimum of 4 years of employment, litigation and/or immigration law experience; 5 years preferred. + Strong understanding of employment, litigation and/or immigration laws. + In-house/pharmaceutical industry and HR experience preferred. + Must be able to multi-task, be detail-oriented, collate data within an internal database, and able to analyze information, and understand client needs. + Proven project management experience. + Excellent oral/written communication. Demonstrated analytical and interpersonal skills. Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: + The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. + We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. + This job is eligible to participate in our short-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit ************************************************************************* US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: ************************************************************* Salary: $106,500 - $202,500
    $106.5k-202.5k yearly 15d ago
  • In-House Counsel

    Vanda Pharmaceuticals 4.5company rating

    Washington, DC jobs

    Responsibilities: Provide general support to the company‘s legal department Assist with researching, drafting, and managing corporate policies Ensure company compliance with legal policies, state and federal laws, and regulations Draft and review contracts Gather, organize, and store information relevant to ongoing projects Work with industry-leading outside counsel Identify potential legal risks to the company Maintain the company's legal files including a library of pre-approved form documents, templates, and historical documents; add or revise material as needed Provide support for litigation and regulatory-related matters Learn something new every day, become conversant in dozens of highly technical topics, develop proficiencies Perform other related duties as requested or as responsibilities dictate Qualifications: Minimum of a J.D. Law Degree; minimum of 1 - 2 years of legal experience a plus Licensed (or about to become licensed in 2025) to practice law in the United States Strong interpersonal skills, work ethic, and ability to work independently Ability to identify underlying issues in complex situations Excellent written and verbal communication skills Ability to juggle multiple priorities, organize time, meet deadlines, and deal with highly confidential information Ability to make decisions and justify legal recommendations Customer service oriented and a positive attitude Willingness to 'roll up your sleeves' and learn every day Strong proficiency with the Microsoft Office Suite Must be able to perform the essential functions of the position, with or without reasonable accommodation; however, reasonable accommodations will be provided for qualified individuals with disabilities unless doing so would impose undue hardship. The total compensation package for this position will also include incentive compensation and benefits such as health insurance, unlimited paid time off, parental leave, a 401k matching program, and other benefits to its employees. We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, gender identity, sexual orientation, protected veteran status, or any other characteristic protected by law. If you reside in a state or locality with enacted pay transparency laws, you are entitled to request and receive additional details regarding compensation and benefits. For assistance, please contact us at ************ between 8:00 AM and 5:30 PM ET, Monday through Friday.
    $94k-166k yearly est. 60d+ ago
  • Associate Counsel, Employment & Immigration

    Abbvie 4.7company rating

    North Chicago, IL jobs

    AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at ************** . Follow @abbvie on X , Facebook , Instagram , YouTube , LinkedIn and Tik Tok . Job Description The Employment and Immigration Associate Counsel is responsible for providing U.S. employment and immigration law guidance and support to AbbVie's global pharmaceutical business. In partnership with AbbVie's employment and immigration law attorneys, this attorney will help manage AbbVie's U.S. immigration program portfolio and provide legal counsel to clients regarding employment and immigration laws. The attorney will interface with internal and outside legal counsel and stakeholders. This position reports to the VP, Employment, Immigration & Labor. This position requires the individual to work a hybrid work schedule of three days a week at the designated work site in North Chicago, IL. Core Job Responsibilities : Manage and maintain a portfolio of U.S. business immigration matters in compliance with U.S. immigration laws and AbbVie policies. Manage relationships with AbbVie's outside counsel. Advise and represent AbbVie on workplace employment issues including government agency charges and attorney demand letters. Prepare substantive written responses. Provide counseling to Human Resources regarding employment and immigration matters. Communicate with internal clients regarding employment and immigration laws. Provide legal support on AbbVie policies, agreements, compliance initiatives and projects. Qualifications JD degree and appropriate licensure to practice law in Illinois. Minimum of 4 years of employment, litigation and/or immigration law experience; 5 years preferred. Strong understanding of employment, litigation and/or immigration laws. In-house/pharmaceutical industry and HR experience preferred. Must be able to multi-task, be detail-oriented, collate data within an internal database, and able to analyze information, and understand client needs. Proven project management experience. Excellent oral/written communication. Demonstrated analytical and interpersonal skills. Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. This job is eligible to participate in our short-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://**************/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://**************/join-us/reasonable-accommodations.html
    $130k-173k yearly est. 2d ago
  • Associate Counsel, Employment & Immigration

    Abbvie 4.7company rating

    North Chicago, IL jobs

    AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at *************** Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok. Job Description The Employment and Immigration Associate Counsel is responsible for providing U.S. employment and immigration law guidance and support to AbbVie's global pharmaceutical business. In partnership with AbbVie's employment and immigration law attorneys, this attorney will help manage AbbVie's U.S. immigration program portfolio and provide legal counsel to clients regarding employment and immigration laws. The attorney will interface with internal and outside legal counsel and stakeholders. This position reports to the VP, Employment, Immigration & Labor. This position requires the individual to work a hybrid work schedule of three days a week at the designated work site in North Chicago, IL. Core Job Responsibilities: Manage and maintain a portfolio of U.S. business immigration matters in compliance with U.S. immigration laws and AbbVie policies. Manage relationships with AbbVie's outside counsel. Advise and represent AbbVie on workplace employment issues including government agency charges and attorney demand letters. Prepare substantive written responses. Provide counseling to Human Resources regarding employment and immigration matters. Communicate with internal clients regarding employment and immigration laws. Provide legal support on AbbVie policies, agreements, compliance initiatives and projects. Qualifications JD degree and appropriate licensure to practice law in Illinois. Minimum of 4 years of employment, litigation and/or immigration law experience; 5 years preferred. Strong understanding of employment, litigation and/or immigration laws. In-house/pharmaceutical industry and HR experience preferred. Must be able to multi-task, be detail-oriented, collate data within an internal database, and able to analyze information, and understand client needs. Proven project management experience. Excellent oral/written communication. Demonstrated analytical and interpersonal skills. Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. This job is eligible to participate in our short-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit ************************************************************************* US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: *************************************************************
    $130k-173k yearly est. 14d ago
  • North Carolina Associate Attorney

    Us Default Group Inc. 4.2company rating

    Charlotte, NC jobs

    North Carolina Associate Attorney - Creditors' Rights Law Firm RAS LaVrar, LLC is an elite creditors' rights law firm that provides full service litigation in addition to comprehensive collection services. The NC Associate Attorney role provides the opportunity for the right candidate to immerse themselves in responsibilities for the North Carolina office. Our firm maintains a collegial work environment that prioritizes internal promotion, training, and professional development. We strive to see our employees grow! We are seeking 1-2 years litigation or collections experience and a candidate that can prioritize workloads to meet deadlines, exhibit meticulous attention to detail, produce accurate and high-quality work product in a fast-paced volume-based environment. The candidate must be able to work independently and possess strong interpersonal and analytical skills. Bar membership in North Carolina is required. Compensation will be commensurate with experience, and includes our benefits package. Additional compensation and special consideration will be given to candidates licensed to practice law, or who become licensed in Florida, Georgia, South Carolina, Virginia, and/or Pennsylvania. We are looking to hire a candidate with the aforementioned bar membership(s) who lives in Charlotte or the surrounding area. Job Responsibilities - in this role, you will… · Assist with managing the firm's North Carolina practice · Handle hearings in the state of North Carolina · Monitor progress and develop strategies to bring files to resolution effectively and efficiently · Provide comprehensive review of all conditions precedent to filing of the action, including review of documents, financials, notices and demand letters · Draft and review pleadings and correspondence to initiate actions · Ensure all internal systems are updated to include findings, documentation, and recommendations · Exercise a high degree of confidentiality and professionalism · Safeguard compliance with local, state, and federal foreclosure, bankruptcy, and collections requirements, as applicable · Handle contested matters, including discovery and trials. Requisite Knowledge, Skills, and Abilities · Intermediate to advanced-level computer and general office skills · Strong interpersonal skills · Ability to effectively communicate through both verbal and written electronic correspondence · Demonstrated ability to analyze corrective action opportunities and present recommendations · Meticulous analytical, organizational skills and attention to detail · Ability to work independently Required Education and Training · Juris Doctor · Bar membership in North Carolina Preferred Qualifications 1-3 years legal experience - preferred Legal collections experience - preferred
    $52k-90k yearly est. Auto-Apply 60d+ ago
  • Associate Counsel, Risk Management and Litigation

    Arthrex, Inc. 4.8company rating

    Naples, FL jobs

    Requisition ID: 64386 Title: Associate Risk Management and Litigation Counsel Division: Arthrex, Inc. (US01) Location: INC - Arthrex One (US33) Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex is actively searching for an Associate Risk Management and Litigation Counsel to join our legal team. Join our talented team at a global medical device company focused on Helping Surgeons Treat Their Patients Better. Main Objective: Provide Responsible for protecting the organization's legal interests and maintaining its operations within the scope established by law. Essential Duties and Responsibilities: * Provides support for all litigation and claims management needs of the department. * Assists with the defense of litigation, product liability issues, insurance correspondence, regulatory matters, and internal investigations. * Assists with document review, e-discovery and case management, as needed. * Responsible for presenting clear recommendations back to the business and assuring legal compliance. * Advise on claim status, legal risks, and the legal liabilities associated with medical device manufacturing and distribution. * Represent the department as required in liaison with outside counsel for depositions, witness preparation, mediations, and interviews. * Review marketing and advertising materials to ensure compliance with legal and regulatory requirements. * Drafts simple and complex memorandum on various legal topics including but not limited to those related to medical device manufacturers. * Provides timely advice and counsel to senior management by advising the business on laws, regulations, and company policies. * Ability to deliver high-quality work under deadlines. * May supervise legal support staff * Up to 10% travel may be required. Education and Experience: * Must be a graduate of an accredited law school * 5 years' experience required as an attorney in litigation within a law firm and/or in house setting * Must be admitted into and a member in good standing of a state bar * Experience in the medical device, pharmaceutical, or life sciences industry preferred Knowledge and Skill Requirements/Specialized Courses and/or Training: Advanced writing, comprehensive reading, communication and research skills required. Electronic based legal research experience required. Machine, Tools, and/or Equipment Skills: LEXIS/Westlaw, Excel, MS Office, PC, printer, copiers and other miscellaneous office equipment Arthrex Benefits * Medical, Dental and Vision Insurance * Company-Provided Life Insurance * Voluntary Life Insurance * Flexible Spending Account (FSA) * Supplemental Insurance Plans (Accident, Cancer, Hospital, Critical Illness) * Matching 401(k) Retirement Plan * Annual Bonus * Wellness Incentive Program * Free Onsite Medical Clinics * Free Onsite Lunch * Tuition Reimbursement Program * Trip of a Lifetime * Paid Parental Leave * Paid Time Off * Volunteer PTO * Employee Assistance Provider (EAP) All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other status protected by law. Making People Better at Arthrex Lorem ipsum dolor sit amet consectetur. Cras fringilla elementum odio velit. Job Details Date: Jan 1, 2026 Requisition ID: 64386 Salary Range: Job title: Associate Counsel, Risk Management and Litigation Arthrex Location: Naples, FL, US, 34108 Nearest Major Market: Naples Job Segment: Medical Device, Marketing Manager, Orthopedic, Manager, Advertising, Healthcare, Marketing, Management
    $85k-132k yearly est. 48d ago
  • HSE External Partner Associate

    Eli Lilly and Company 4.6company rating

    Indianapolis, IN jobs

    At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. This role supports the HSE External Partner Program in managing health, safety, and environmental risks across Lilly Research Labs' (LRL) global external partner network. This role provides operational support for partner assessments, data management, and program administration. External Partner Engagement and Qualification Supports the qualification and screening of external partners through the Lilly Research Labs (LRL) risk management oversight program (PQA), focusing on evaluating HSE capabilities to ensure alignment with HSE regulatory requirements and Lilly HSE expectations. Leads the HSE screening process by initiating outreach to prospective partners, distributing tailored HSE questionnaires, and conducting virtual assessments to validate the partner's ability to meet safety and compliance requirements. Collaborates cross-functionally with internal LRL partners including discovery, small molecule, biologics, devices, clinical development, and packaging teams to ensure that HSE risks are appropriately identified and mitigated prior to project initiation. Onsite External Partner Assessment and Support Coordinates assessment scheduling across multiple time zones, managing calendar coordination between internal partners and external partners. Assists with conducting comprehensive HSE capability and risk assessments across all multiple evaluation rubrics (environmental management, industrial hygiene, HSE management systems, general safety, emergency preparedness, and process safety management). Prepares detailed HSE risk assessment reports, including formal findings, opportunities for improvement, and action items with specific recommendations aligned to the HSE evaluation rubrics. Supports CAPA (Corrective and Preventive Action) tracking by monitoring partner response, timelines, verifying completion of corrective actions, and maintaining closure documentation. Supports partner performance reviews by preparing performance summaries. Assists in the ongoing HSE monitoring and assessments to track external partner HSE performance through routine re-assessments (virtual and onsite). Technical HSE Consultation and Resource Assists in providing strategic HSE guidance to Lilly partners by serving as a HSE subject matter expert and technical consultant in the HSE risk management for external partners managing Lilly projects. Serves as technical resource for complex HSE challenges including exposure and containment strategy development and planning especially for critical and strategic partnerships. Facilitates HSE related information exchanges between LRL and external partners ensuring timely communication of requirements and expectations. Provide support as a HSE liaison during partner-related incidents including immediate response coordination, investigation and corrective action oversight. Program Development and Continuous Improvement Contributes to the maintenance and evolution of assessment tools and processes, and communication strategies required for the effective management of the HSE external partner program. Leads development of digital tools and automation to streamline partner assessment processes, improve data quality, and enhance reporting capabilities. Assists with process standardization by documenting workflows, creating templates, and supporting change management activities. Maintain an up-to-date knowledge of emerging issues in both HSE and Discovery/R&D that will allow the business to identify and manage risk as well as help shape policy and prioritize activities Strategic Collaboration and Internal Alignment Engages in cross-functional project teams supporting broader LRL initiatives that involve external partner engagement. Supports benchmarking and industry collaboration activities with PSCI. Basic Requirements Master's degree in industrial Hygiene, Environmental Health and Safety, Engineering or Sciences or relevant degree related to Health, Safety, and Environmental. 5+ years' experience in HSE preferably in R&D pharmaceutical or biotech environments. 3+ years of experience in third-party or contractor HSE management with assessment or auditing oversight. Additional Skills/Preferences HSE experience including deep technical knowledge in at least industrial hygiene and exposure control AND at least one other HSE evaluation rubric (environmental management, industrial hygiene, HSE management systems, general safety and emergency preparedness, and process safety management). Working knowledge of HSE evaluation rubrics with ability to develop expertise in remaining areas. Strong cross-cultural communication and partner engagement skills. Ability to manage complex logistics across time zones and regulatory frameworks. Excellent written and verbal communication skills. Professional certifications preferred (CIH, CSP, CHMM, or equivalent international certifications). Ability to assess HSE risks across multiple functional areas, including discovery research, small molecule and biologic development, device development, clinical operations, and packaging. Requires working knowledge of processes and hazards in each of these functional areas in order to evaluate partner capabilities and risks. Proficiency in interpreting technical documentation and synthesizing findings into actionable reports. Advanced analytical and problem-solving capabilities with ability to synthesize complex technical information and develop practical solutions. Project management skills including ability to manage multiple partner assessments simultaneously while maintaining quality and deadlines. Technology proficiency including experience with database systems, and digital assessment tools. Flexibility and learning agility, including ability to appropriately prioritize workload and quickly shift priorities Additional Information Domestic and international travel is required. Travel timing can be scheduled and managed but should anticipate as much as 50% travel. Tasks will require entering manufacturing and laboratory areas, which require wearing appropriate PPE. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (******************************************************** for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), en Able (for people with disabilities). Learn more about all of our groups. Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $63,000 - $162,800 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. #WeAreLilly
    $63k-162.8k yearly Auto-Apply 60d+ ago
  • HSE External Partner Associate

    Eli Lilly and Company 4.6company rating

    Gas City, IN jobs

    At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. This role supports the HSE External Partner Program in managing health, safety, and environmental risks across Lilly Research Labs' (LRL) global external partner network. This role provides operational support for partner assessments, data management, and program administration. External Partner Engagement and Qualification Supports the qualification and screening of external partners through the Lilly Research Labs (LRL) risk management oversight program (PQA), focusing on evaluating HSE capabilities to ensure alignment with HSE regulatory requirements and Lilly HSE expectations. Leads the HSE screening process by initiating outreach to prospective partners, distributing tailored HSE questionnaires, and conducting virtual assessments to validate the partner's ability to meet safety and compliance requirements. Collaborates cross-functionally with internal LRL partners including discovery, small molecule, biologics, devices, clinical development, and packaging teams to ensure that HSE risks are appropriately identified and mitigated prior to project initiation. Onsite External Partner Assessment and Support Coordinates assessment scheduling across multiple time zones, managing calendar coordination between internal partners and external partners. Assists with conducting comprehensive HSE capability and risk assessments across all multiple evaluation rubrics (environmental management, industrial hygiene, HSE management systems, general safety, emergency preparedness, and process safety management). Prepares detailed HSE risk assessment reports, including formal findings, opportunities for improvement, and action items with specific recommendations aligned to the HSE evaluation rubrics. Supports CAPA (Corrective and Preventive Action) tracking by monitoring partner response, timelines, verifying completion of corrective actions, and maintaining closure documentation. Supports partner performance reviews by preparing performance summaries. Assists in the ongoing HSE monitoring and assessments to track external partner HSE performance through routine re-assessments (virtual and onsite). Technical HSE Consultation and Resource Assists in providing strategic HSE guidance to Lilly partners by serving as a HSE subject matter expert and technical consultant in the HSE risk management for external partners managing Lilly projects. Serves as technical resource for complex HSE challenges including exposure and containment strategy development and planning especially for critical and strategic partnerships. Facilitates HSE related information exchanges between LRL and external partners ensuring timely communication of requirements and expectations. Provide support as a HSE liaison during partner-related incidents including immediate response coordination, investigation and corrective action oversight. Program Development and Continuous Improvement Contributes to the maintenance and evolution of assessment tools and processes, and communication strategies required for the effective management of the HSE external partner program. Leads development of digital tools and automation to streamline partner assessment processes, improve data quality, and enhance reporting capabilities. Assists with process standardization by documenting workflows, creating templates, and supporting change management activities. Maintain an up-to-date knowledge of emerging issues in both HSE and Discovery/R&D that will allow the business to identify and manage risk as well as help shape policy and prioritize activities Strategic Collaboration and Internal Alignment Engages in cross-functional project teams supporting broader LRL initiatives that involve external partner engagement. Supports benchmarking and industry collaboration activities with PSCI. Basic Requirements Master's degree in industrial Hygiene, Environmental Health and Safety, Engineering or Sciences or relevant degree related to Health, Safety, and Environmental. 5+ years' experience in HSE preferably in R&D pharmaceutical or biotech environments. 3+ years of experience in third-party or contractor HSE management with assessment or auditing oversight. Additional Skills/Preferences HSE experience including deep technical knowledge in at least industrial hygiene and exposure control AND at least one other HSE evaluation rubric (environmental management, industrial hygiene, HSE management systems, general safety and emergency preparedness, and process safety management). Working knowledge of HSE evaluation rubrics with ability to develop expertise in remaining areas. Strong cross-cultural communication and partner engagement skills. Ability to manage complex logistics across time zones and regulatory frameworks. Excellent written and verbal communication skills. Professional certifications preferred (CIH, CSP, CHMM, or equivalent international certifications). Ability to assess HSE risks across multiple functional areas, including discovery research, small molecule and biologic development, device development, clinical operations, and packaging. Requires working knowledge of processes and hazards in each of these functional areas in order to evaluate partner capabilities and risks. Proficiency in interpreting technical documentation and synthesizing findings into actionable reports. Advanced analytical and problem-solving capabilities with ability to synthesize complex technical information and develop practical solutions. Project management skills including ability to manage multiple partner assessments simultaneously while maintaining quality and deadlines. Technology proficiency including experience with database systems, and digital assessment tools. Flexibility and learning agility, including ability to appropriately prioritize workload and quickly shift priorities Additional Information Domestic and international travel is required. Travel timing can be scheduled and managed but should anticipate as much as 50% travel. Tasks will require entering manufacturing and laboratory areas, which require wearing appropriate PPE. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (******************************************************** for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), en Able (for people with disabilities). Learn more about all of our groups. Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $63,000 - $162,800 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. #WeAreLilly
    $63k-162.8k yearly Auto-Apply 60d+ ago
  • Staff Attorney - Tarrytown

    ENT and Allergy Associates 4.5company rating

    White Plains, NY jobs

    ENT and Allergy Associates/Quality Medical Management Services, New York & New Jersey's premier ENT and Allergy medical practice, is seeking a a detail-oriented and proactive Staff Attorney to join our legal team. Salary: $150,000-$157,000/year This role will be responsible for drafting and reviewing contracts, overseeing litigation matters, ensuring regulatory compliance, and providing legal guidance on various business operations. The ideal candidate will have experience in healthcare law, employment law, and contract management, with the ability to collaborate effectively with internal teams and outside counsel. Key Responsibilities: Draft employment contracts, amendments to employment contracts, joinders and amendments to ENTA Partnership Agreement Review and edit property leases and amendments to property leases Provide oversight over litigation including but not limited to employment related, medical malpractice and regulatory Work with Director of Regulatory Affairs to assist on healthcare compliance/regulatory legal issues Work with Chief Strategy Officer and other team members on managed care contracting matters and outside counsel if needed Review subpoenas, medical records requests and legal complaints and provide legal advice surrounding same Assist internal legal team in managed services organization (MSO) related agreements and legal issues Assist internal legal team with risk retention group (RRG) legal issues and documents Work with outside counsel on a variety of legal issues Assist internal legal team in becoming more streamlined and organized with respect to contract management capabilities Assist risk management team in providing legal advice on reducing risk across the business Draft and edit settlement agreements with patients and employees Handle small claims court matters on occasion Qualifications: Juris Doctor (J.D.) degree from an accredited law school. Admitted to NY and/or NJ bar preferred 3+ years of experience in corporate, healthcare, or employment law. Strong knowledge of contract law, regulatory compliance, and litigation management. Excellent legal research, drafting, and negotiation skills. Ability to work independently and collaboratively in a fast-paced environment. Strong attention to detail and organizational skills. Must be willing to work at Corporate office located on Tarrytown NY We offer a competitive salary with a comprehensive benefits package including: Medical/Dental/Vision insurance, Company paid long term disability, Flexible spending account, Company paid life insurance, Voluntary life insurance, 401k, Pet insurance. Please note: ENT and Allergy Associates, LLP and Quality Medical Management Services USA, LLC is an E-Verify employer. Company Description: ENT and Allergy Associates, LLP is the largest and most comprehensive ear, nose, throat, allergy and audiology practice in the nation with over 60 offices and over 300 physicians. Each ENT and Allergy Associates clinical location provides access to a full complement of services, including General Adult and Pediatric ENT, Voice and Swallowing, Facial Plastics and Reconstructive Surgery, Disorders of the Inner Ear and Dizziness, Asthma, Clinical Immunology, Diagnostic Audiology, Hearing Aid dispensing, Sleep and CT Services. ENTA has a clinical alliance with The Mount Sinai Hospital for the treatment of diseases of the head and neck and esophageal cancer and a partnership with the American Cancer Society to educate and treat patients with smoking disorders and cancer. The Practice has also expanded its clinical capabilities to include advanced Immunodeficiency trials. To learn more about the benefits of ENT and Allergy Associates, or to conveniently find an ENT doctor or Allergy Doctor and then easily book an appointment at the nearest New York or New Jersey location, please visit: ********************* or contact us at: ENT and Allergy Associates, LLP 660 White Plains Road, 4th Floor Tarrytown, NY 10591 ENT and Allergy Associates is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
    $150k-157k yearly Auto-Apply 60d+ ago
  • Associate Counselor, FT

    STEL 3.5company rating

    Jamestown, NY jobs

    Southern Tier Environments for Living, Inc. EMPLOYMENT OPPORTUNITY STEL, Inc. is the Chautauqua - Allegheny region's leading and largest mental health residential rehabilitation and support provider. We seek caring, empathetic and energetic people to join our team of professionals to support our mission assisting people in recovery from mental illness. PAID TRAINING PROVIDED. Competitive salary and excellent full time benefits package including medical, dental, vision, Sec.125 plan, retirement plan, employee assistance plan and more. APPLY TODAY! JOB TITLE: ASSOCIATE COUNSELOR, Full-Time DEPARTMENT: Prendergast Avenue Residence - Jamestown, NY HOURS: Tuesday through Saturday 7:00 am to 3:00 pm MINIMUM SALARY: $17.37 per hour AVAILABLE: ASAP JOB FUNCTION: Performs direct care work teaching adult daily living skills and supervising residents in agency community residence or apartment program. Supportive counseling and daily household tasks. MINIMUM QUALIFICATIONS: Education, Experience, and Knowledge High School diploma or equivalent required. Associates degree in Human Services and/or one year experience working with people with mental illness preferred. Prefer a working knowledge of current issues and concerns of people with mental illness, rehabilitative training methods, and community resources. Other Qualifications Have a home telephone. Be able to travel to and among various facilities that are multileveled with stairs only. Have a valid driver's license and a safe driving record. May be required to use personal vehicle for programmatic purposes. REPLY TO: Janine Tomczak STEL, Inc. 715 Central Avenue Dunkirk, NY 14048 ***************** Apply on line at *********************** or email ************* INTERNAL CANDIDATES: Please forward “In House” application. Updated resume is required. EXTERNAL CANDIDATES: Please apply at stel.org/careers EQUAL OPPORTUNITY EMPLOYER
    $17.4 hourly Easy Apply 60d+ ago
  • Commercial Contracts Attorney

    Medpace 4.5company rating

    Cincinnati, OH jobs

    We are looking to introduce a full-time Contracts Attorney to expand our Commercial Operations team. The Contracts Attorney will play a key role in the development and management of contracts with Medpace's clients, pharmaceutical companies, and strategic vendors for clinical research trials. Responsibilities * Prepare, negotiate, and finalize customer-related contracts including master services agreements, statements of work, CDAs, and/or other related contracts; * Facilitate clear communication, evaluations and reporting of ongoing contract negotiations; * Independently review and draft contracts, and lead negotiation of strategic contracts; * Work collaboratively with business partners; * Evaluation of legal, financial and business risks associated with contracts in compliance with company policies, in order to protect company interests; and * Design and participate in initiatives relating to contract management and compliance. Qualifications * Juris Doctorate with 3-5 years of contracting experience; * Licensed in Ohio or the ability to obtain Corporate Counsel status in Ohio; * Knowledge of relevant Clinical Trial and Contracts Legislation; * Excellent communication, negotiation and leadership skills; and * Professional demeanor and strong work ethic. Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Cincinnati Perks * Cincinnati Campus Overview * Flexible work environment * Competitive PTO packages, starting at 20+ days * Competitive compensation and benefits package * Company-sponsored employee appreciation events * Employee health and wellness initiatives * Community involvement with local nonprofit organizations * Discounts on local sports games, fitness gyms and attractions * Modern, ecofriendly campus with an on-site fitness center * Structured career paths with opportunities for professional growth * Discounted tuition for UC online programs Awards * Named a Top Workplace in 2024 by The Cincinnati Enquirer * Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
    $41k-71k yearly est. Auto-Apply 13d ago
  • Associate Counselor - Per Diem - Part-Time Relief

    STEL 3.5company rating

    Wellsville, NY jobs

    SOUTHERN TIER ENVIRONMENTS FOR LIVING, INC. Employment Opportunity STEL, Inc. is the Chautauqua-Allegheny region's leading and largest mental health residential rehabilitation and support provider. We seek caring, empathetic, and energetic people to join our team of professionals and support our mission of assisting people in recovery from mental illness. We offer a competitive salary and an excellent full-time benefits package, including medical, dental, vision, Sec.125 plan, retirement plan, employee assistance plan, and more. APPLY TODAY! Associate Counselor - Per Diem - Part-Time Relief DEPARTMENT: Wellsville Community Residence Program - Wellsville, NY SCHEDULE: NO SET SCHEDULE Need to be readily available and flexible to cover call ins for the following shifts when needed. 4:00 pm to 10:00 pm, or 12:00 am to 8:00 pm, or weekends 12:00 pm to 8:00 pm SALARY: Minimum $17.37/hr. AVAILABLE: ASAP JOB FUNCTION: Performs direct care work teaching adult daily living skills and supervising residents in agency community residence or apartment program. Duties include performing daily household tasks and providing supportive counseling and related therapeutic services to people with mental illness. MINIMUM QUALIFICATIONS: Education, Experience, and Knowledge High School/GED diploma or equivalent required. Associates degree in Human Services and/or one year experience working with people with mental illness preferred. Prefer a working knowledge of current issues and concerns of people with mental illness, rehabilitative training methods, and community resources. Excellent customer service skills. Other Qualifications Have a home telephone. Be able to travel to and among various facilities that are multi-leveled with stairs only. Have a valid driver's license and a safe driving record. May be required to use personal vehicle for programmatic purposes. Must pass criminal background checks are required my NYS Office of Mental Health, NYS OMIG, and other regulatory agencies. REPLY TO: Janie Tomczak STEL, Inc. 715 Central Avenue Dunkirk, NY 14048 ***************** Apply on line at *********************** or email ************* INTERNAL CANDIDATES: Please forward “In House” application. Updated resume is required. EXTERNAL CANDIDATES: Please apply at stel.org/careers DEADLINE: Internal Candidates: Until position is filled. DEADLINE: External Candidates: Until position is filled. EQUAL OPPORTUNITY EMPLOYER
    $17.4 hourly Easy Apply 60d+ ago

Learn more about Merck jobs

View all jobs