Research fellow jobs in Bridgeport, CT

The Clinical Development and Medical Affairs Fellow is a post-doctoral pharmacist position that will obtain broad exposure to BI US Medical functions including, but not limited to -- Medical Affairs and Scientific Communications, clinical operations, translational medicine and clinical pharmacology, and regulatory affairs. This position will require the Fellow to develop competencies necessary to contribute to their respective functional area within a pharmaceutical company. The Fellow will be based at Boehringer Ingelheim´s U.S. headquarters in Ridgefield, CT, working on a particular or multiple therapeutic areas (TAs) in the areas of cardiology, diabetes, immunology, oncology, and respiratory. Through a series of rotations either within or outside of the assigned area, the Fellow will also gain an understanding of the broad range of opportunities available to a pharmacist in the pharmaceutical industry. As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies´ success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim´s high regard for our employees. The Regulatory Policy and Intelligence Fellowship is designed to provide pharmacists with exposure to regulatory intelligence and policy activity within the pharmaceutical industry. The position will also offer the opportunity to complete rotations in areas within and beyond Regulatory Affairs. The Fellow will be exposed to projects involving both US marketed products and investigational projects. Under supervision, the Fellow will: - Develop, compile, and integrate regulatory intelligence from health authorities, professional groups, publicly available information and BI. - Appropriately communicate regulatory intelligence within the organization. - Provide analysis, advice, and guidance on US regulatory strategies to promote expedited product development and approval. - Research information on regulatory policies and departmental policies within and external to RA. - Research and implement processes to improve regulatory intelligence and collaboration. - Develop expertise on projects from the regulatory intelligence and policy perspective. - Collaborate with BI Government Affairs to ensure knowledge sharing of overlapping intelligence topics. **Duties & Responsibilities** **Regulatory Expertise:** The Fellow will develop basic regulatory policy and intelligence knowledge across the spectrum of BI assets and marketed products. Interact effectively within Regulatory Affairs and across functions, as a US regulatory advocate to achieve common goals for assigned projects, with supervision. With supervision, the Regulatory Policy and Intelligence Fellow will: + Proactively review and evaluate relevant US regulations and guidelines, as well as evolving regulatory trends and developments for their impact on drug and device development activities and on existing development strategies. + Lead requests for global country-level regulatory information from various partners. + Handle the development of custom reports to support regulatory compliance and advise strategy. + Collaborate with partners to support any compliance and process initiatives. + Own the review and refinement of regulatory FDA guidance and recommendations by developing written comments reflecting BI's priorities for submission to health authorities. + Supervise the evaluation of new regulatory intelligence data sources and service providers. + Serve as Regulatory intelligence lead on highly sophisticated cross-functional teams. + Provide regular communications and briefings to global and regional policy management on relevant global regulatory policy issues. + Participate in internal product team meetings to provide regulatory policy context for business decisions. + Provide strategic regulatory advice to RA colleagues on drug development and device projects, registration, and marketed products in preparation for HA meetings. + Develop training materials and participate as a facility member on new and emerging regulatory requirements for RA colleagues and other line functions. + Analyze impact of important emerging regulatory policies and new requirements on projects and business. + Prepare and coordinate internal customer feedback on proposed laws, regulations and guidances, to ensure consideration of BI's positions by trade organizations. + When appropriate, collaborate with Government Affairs to shape emerging legislative proposals. + Develop targeted and appropriate automation of regulatory information. **Position Expertise:** + Basic knowledge of pharmacy gained through Doctor of Pharmacy program + Fellow should have basic understanding of: + Food, Drug and Cosmetic Act. + 21 CFR regulations relevant to drug/biologic development and registration. + Other relevant US laws, regulations and guidance documents. + Medical, pharmaceutical and scientific knowledge and understanding in the assigned therapeutic area. **Application Requirements** **1. Curriculum vitae** **2. Letter of intent** - focusing on how a fellowship at Boehringer Ingelheim can help further your career growth. ***** Please upload under My Documents, Additional Attachments. **Requirements** + Doctor of Pharmacy degree from an ACPE-accredited school or college of pharmacy earned prior to the start date at Boehringer Ingelheim. + Ability to perform MEDLINE and EMBASE literature searches. + Strong intrapersonal, active listening, and problem-solving skills with an ability to work well in a team environment. + Highly motivated and shows initiative in contributing to team deliverables. + Receptive to receiving and quickly implementing constructive feedback. + Ability to work independently within provided guidance from team leads. + Adaptable and able to contribute to multiple Therapeutic Areas as needed. + Excellent verbal and written communication skills. + Proven experience working in a dynamic, high volume environment handling multiple tasks. + Strong computer skills, including Outlook, Word, PowerPoint, and Excel. + Foundational understanding of corporate structure, regulatory considerations and the drug development process in pharmacy with an ability to quickly adapt to a changing Corporate environment that will allow the incumbent to be productive in rotational experiences. Desired Experience, Skills, and Abilities: + Prior pharmaceutical industry experience (e.g. internship or Advanced Pharmacy Practice Experience [APPE] rotation is preferred but not required. All qualified applicants will receive consideration for employment without regard to a person's actual or perceived race, including natural hairstyles, hair texture and protective hairstyles; color; creed; religion; national origin; age; ancestry; citizenship status, marital status; gender, gender identity or expression; sexual orientation, mental, physical or intellectual disability, veteran status; pregnancy, childbirth or related medical condition; genetic information (including the refusal to submit to genetic testing) or any other class or characteristic protected by applicable law.

Behavioral Health Research Scientist Position specific details: This is a Health Research role where the successful hire will conduct data analysis, review and incorporation of relevant literature, collaborative project design, associated data collection activities including extracting and manipulating data, use statistical methods to analyze data and generate useful reports depicting trends in performance measures, conducting basic statistical analysis, report writing, and presenting results at committee meetings. This is not an IT role. Will also be responsible for understanding and assisting with updating performance measure methodology, including reporting and data requirements, and using quality improvement techniques to improve organizational and/or provider performance. Hybrid 1: This role requires associates to be in-office 1-2 days per week, fostering collaboration and connectivity, while providing flexibility to support productivity and work-life balance. This approach combines structured office engagement with the autonomy of virtual work, promoting a dynamic and adaptable workplace. The ideal candidate will be within a reasonable distance of our Rocky Hill, CT or Wallingford, CT office. Please note that per our policy on hybrid/virtual work, candidates not within a reasonable commuting distance from the posting location(s) will not be considered for employment, unless an accommodation is granted as required by law. The Health Research Scientist - Connecticut creates statistical models to predict, classify, quantify, and/or forecast behavioral health (BH) outcomes. business metrics. Design modeling studies to address specific issues determined by consultation with internal and external partners. How You Will Make an Impact: * Prepares analytical data sets based on Medicaid claims and authorization data in support of modeling studies. * Build, test, and validate statistical models. * Publishes results and address constraints/limitations with high level partners. * Proactively collaborates interdepartmentally to determine identified population segments and develop actionable plans to enable the identification of patterns related to quality, use, cost and other variables. Minimum Requirement: * Requires MS, MA, or PhD with concentration in a quantitative discipline such as statistics, cognitive science, economics, or operations research; a minimum of 3 years direct experience programming large, multi-source datasets with SAS required, and a minimum of 3 years in health care setting; or any combination of education and experience which would provide an equivalent background. Preferred Skills, Capabilities, and Experiences: * Experience in behavioral health, social studies, social work, psychiatry, or public health is strongly preferred. * Intermediate to Advanced expertise with software such as SAS, SAS Enterprise Miner, Tableau or equivalents strongly preferred. * Proven ability to design research studies and experience with data models, program evaluation, addressing data quality issues in study design, constructing robust and efficient analytical data sets strongly preferred. * Significant experience analyzing claims data strongly preferred. * The ability to present meaningful results to a business audience, to participate collaboratively in a team tasked to produce complex analyses on a rigorous schedule, to communicate with strong written and verbal communications skills, and to present to large multi-disciplinary audiences on a regular basis strongly preferred. * Healthcare/managed care/insurance experience preferred. * Experience with value-based payment models or attribution methodologies. Please be advised that Elevance Health only accepts resumes for compensation from agencies that have a signed agreement with Elevance Health. Any unsolicited resumes, including those submitted to hiring managers, are deemed to be the property of Elevance Health. Who We Are Elevance Health is a health company dedicated to improving lives and communities - and making healthcare simpler. We are a Fortune 25 company with a longstanding history in the healthcare industry, looking for leaders at all levels of the organization who are passionate about making an impact on our members and the communities we serve. How We Work At Elevance Health, we are creating a culture that is designed to advance our strategy but will also lead to personal and professional growth for our associates. Our values and behaviors are the root of our culture. They are how we achieve our strategy, power our business outcomes and drive our shared success - for our consumers, our associates, our communities and our business. We offer a range of market-competitive total rewards that include merit increases, paid holidays, Paid Time Off, and incentive bonus programs (unless covered by a collective bargaining agreement), medical, dental, vision, short and long term disability benefits, 401(k) +match, stock purchase plan, life insurance, wellness programs and financial education resources, to name a few. Elevance Health operates in a Hybrid Workforce Strategy. Unless specified as primarily virtual by the hiring manager, associates are required to work at an Elevance Health location at least once per week, and potentially several times per week. Specific requirements and expectations for time onsite will be discussed as part of the hiring process. The health of our associates and communities is a top priority for Elevance Health. We require all new candidates in certain patient/member-facing roles to become vaccinated against COVID-19 and Influenza. If you are not vaccinated, your offer will be rescinded unless you provide an acceptable explanation. Elevance Health will also follow all relevant federal, state and local laws. Elevance Health is an Equal Employment Opportunity employer and all qualified applicants will receive consideration for employment without regard to age, citizenship status, color, creed, disability, ethnicity, genetic information, gender (including gender identity and gender expression), marital status, national origin, race, religion, sex, sexual orientation, veteran status or any other status or condition protected by applicable federal, state, or local laws. Applicants who require accommodation to participate in the job application process may contact ******************************************** for assistance. Qualified applicants with arrest or conviction records will be considered for employment in accordance with all federal, state, and local laws, including, but not limited to, the Los Angeles County Fair Chance Ordinance and the California Fair Chance Act.

Behavioral Health Research Scientist Position specific details: This is a Health Research role where the successful hire will conduct data analysis, review and incorporation of relevant literature, collaborative project design, associated data collection activities including extracting and manipulating data, use statistical methods to analyze data and generate useful reports depicting trends in performance measures, conducting basic statistical analysis, report writing, and presenting results at committee meetings. This is not an IT role. Will also be responsible for understanding and assisting with updating performance measure methodology, including reporting and data requirements, and using quality improvement techniques to improve organizational and/or provider performance. Hybrid 1: This role requires associates to be in-office 1-2 days per week, fostering collaboration and connectivity, while providing flexibility to support productivity and work-life balance. This approach combines structured office engagement with the autonomy of virtual work, promoting a dynamic and adaptable workplace. The ideal candidate will be within a reasonable distance of our Rocky Hill, CT or Wallingford, CT office. Please note that per our policy on hybrid/virtual work, candidates not within a reasonable commuting distance from the posting location(s) will not be considered for employment, unless an accommodation is granted as required by law. The Health Research Scientist - Connecticut creates statistical models to predict, classify, quantify, and/or forecast behavioral health (BH) outcomes. business metrics. Design modeling studies to address specific issues determined by consultation with internal and external partners. How You Will Make an Impact: Prepares analytical data sets based on Medicaid claims and authorization data in support of modeling studies. Build, test, and validate statistical models. Publishes results and address constraints/limitations with high level partners. Proactively collaborates interdepartmentally to determine identified population segments and develop actionable plans to enable the identification of patterns related to quality, use, cost and other variables. Minimum Requirement: Requires MS, MA, or PhD with concentration in a quantitative discipline such as statistics, cognitive science, economics, or operations research; a minimum of 3 years direct experience programming large, multi-source datasets with SAS required, and a minimum of 3 years in health care setting; or any combination of education and experience which would provide an equivalent background. Preferred Skills, Capabilities, and Experiences: Experience in behavioral health, social studies, social work, psychiatry, or public health is strongly preferred. Intermediate to Advanced expertise with software such as SAS, SAS Enterprise Miner, Tableau or equivalents strongly preferred. Proven ability to design research studies and experience with data models, program evaluation, addressing data quality issues in study design, constructing robust and efficient analytical data sets strongly preferred. Significant experience analyzing claims data strongly preferred. The ability to present meaningful results to a business audience, to participate collaboratively in a team tasked to produce complex analyses on a rigorous schedule, to communicate with strong written and verbal communications skills, and to present to large multi-disciplinary audiences on a regular basis strongly preferred. Healthcare/managed care/insurance experience preferred. Experience with value-based payment models or attribution methodologies. Job Level: Non-Management Exempt Workshift: Job Family: RDA > Reporting & Data Analysis Please be advised that Elevance Health only accepts resumes for compensation from agencies that have a signed agreement with Elevance Health. Any unsolicited resumes, including those submitted to hiring managers, are deemed to be the property of Elevance Health. Who We Are Elevance Health is a health company dedicated to improving lives and communities - and making healthcare simpler. We are a Fortune 25 company with a longstanding history in the healthcare industry, looking for leaders at all levels of the organization who are passionate about making an impact on our members and the communities we serve. How We Work At Elevance Health, we are creating a culture that is designed to advance our strategy but will also lead to personal and professional growth for our associates. Our values and behaviors are the root of our culture. They are how we achieve our strategy, power our business outcomes and drive our shared success - for our consumers, our associates, our communities and our business. We offer a range of market-competitive total rewards that include merit increases, paid holidays, Paid Time Off, and incentive bonus programs (unless covered by a collective bargaining agreement), medical, dental, vision, short and long term disability benefits, 401(k) +match, stock purchase plan, life insurance, wellness programs and financial education resources, to name a few. Elevance Health operates in a Hybrid Workforce Strategy. Unless specified as primarily virtual by the hiring manager, associates are required to work at an Elevance Health location at least once per week, and potentially several times per week. Specific requirements and expectations for time onsite will be discussed as part of the hiring process. The health of our associates and communities is a top priority for Elevance Health. We require all new candidates in certain patient/member-facing roles to become vaccinated against COVID-19 and Influenza. If you are not vaccinated, your offer will be rescinded unless you provide an acceptable explanation. Elevance Health will also follow all relevant federal, state and local laws. Elevance Health is an Equal Employment Opportunity employer, and all qualified applicants will receive consideration for employment without regard to age, citizenship status, color, creed, disability, ethnicity, genetic information, gender (including gender identity and gender expression), marital status, national origin, race, religion, sex, sexual orientation, veteran status or any other status or condition protected by applicable federal, state, or local laws. Applicants who require accommodation to participate in the job application process may contact ******************************************** for assistance. Qualified applicants with arrest or conviction records will be considered for employment in accordance with all federal, state, and local laws, including, but not limited to, the Los Angeles County Fair Chance Ordinance and the California Fair Chance Act.

NYMC seeks a Postdoctoral Fellow in the Department of Cell Biology and Anatomy. The position will be in the Kwak laboratory to study the general mechanisms of enhancer RNAs and RNA condensates. Candidates with a Ph.D. in cell/molecular biology, genetics/genomics, and/or computational biology are encouraged to apply. Successful candidates will develop a research project focused on non-coding genetic variants and mutations in nascent RNA and epigenetic studies using systems biology approaches and CRISPR genome editing methods. The candidate will contribute to the training of research assistants and graduate students and actively participate in lab and department meetings. How to apply: Interested candidates should submit a complete CV, a summary of current and future research interests, and the contact information of three reference. Responsibilities Develop and perform experimental strategies for genome editing of target genes and the analysis of genetic models Conduct advanced laboratory research through data analysis and interpretation, troubleshoot problems, and design new research projects Publish in peer-reviewed journals and participate in grant proposal preparations Actively participate in lab and departmental scientific meetings Supervise and train students and lab staffs Qualifications Education requirement: Ph.D. in molecular biology, genetics, genomics, or computational biology Prior experience: The candidate must have previous experience in molecular biology, genomics and/or bioinformatics. Preference will be given to candidates familiar with experimental and computational techniques for transcriptomic and epigenomic analyses. Minimum Salary USD $48,806.40/Yr. Maximum Salary USD $61,008.00/Yr.

Position Description: The successful candidate will provide quantitative bioanalytical support using LC-MS/MS for a variety of high throughput in vitro ADME profiling assays. In this hands-on role, the candidate will perform sample analyses by mass spectrometry, and will review, interpret and report results. Instruments and software from various vendors including Sciex (Analyst) and Thermo (Excalibur) will be used along with custom internal data processing software to acquire data and process results. The successful candidate will also troubleshoot HPLC and MS instrumentation as necessary. Position Requirements: BS or MS in chemistry, with specialization in analytical chemistry preferred, along with 1 to 5 years of relevant pharmaceutical experience is required. Training or experience in mass spectrometry and separation science, as well as hands-on experience in quantitative LC-MS/MS analysis are desired. Proficiency in general computer software, including vendor specific instrument control and analysis tools, is required. Strong interpersonal and communication skills, both oral and written, are required as is commitment to working as a team player within a multifunctional organization. A working knowledge of allied disciplines such as computer science, lab automation, drug metabolism, pharmacokinetics and synthetic chemistry is helpful. Qualifications The successful candidate will also troubleshoot HPLC and MS instrumentation as necessary. LC-MS/MS analysis BS or MS in chemistry Additional Information Thanks & Regards Riya ************

HistoWiz is the largest online histopathology company, based in New York City. Our mission is to help biomedical researchers find cures by accelerating histopathology and enabling global collaboration. Since inception in 2013, we have doubled our month-over-month sales, driven primarily by customer referrals. We are profitable, won numerous awards and are funded by prestigious investors, including Y-Combinator and Zhenfund. We are seasoned scientists with experience at leading academic institutions and have published high impact research in top journals of biomedicine. We have just completed our Series A and are now looking to scale our business significantly in the coming years. HistoWiz has over 3,000 paying customers globally from top academic institutions (e.g. MSKCC, Harvard, Stanford, HHMI) and pharmaceutical companies (e.g. CRISPR, Johnson & Johnson, Regeneron). We process tissue specimens and digitize all of the results, hosting our client's data on a proprietary platform, PathologyMapTM . This platform not only enables industry-leading turnaround time for diagnosis, but also online viewing, sharing and search. No other platform like this exists, so we are truly building something new that can bridge scientists, doctors, and patients from all over the world to conquer life-threatening diseases collaboratively instead of individually. This online platform also contains the world's largest collection of pathology data and the first network of top pathologists. We are looking for highly motivated Research Associate to join our fast-growing team. Under the general direction and supervision of the Director of Laboratory Operations, the Research Associate will effectively apply a working knowledge and skill of designated Research Associate-related duties and tasks, in support of the Department as a whole, to complete the daily assigned Histology workload. Requirements Research and review the literature to find the best antibodies for IHC and IF Design and recommend processes, systems, and operational changes to increase efficiency and effectiveness Maintain laboratory organization and team priorities to complete projects with client-expected turnaround time Lead project update meetings with clients Design experiments and interpret results, while thinking critically about research projects Write IHC validation reports for pharma clients Coordinate in ordering supplies and maintain inventory for the AIR department Develop new protocols and assays, including Multiplex mIF panels Troubleshoot quality issues and work with pathologists to QC slides Oversee and perform biomarker and equipment validations Perform IHC, IF and ISH via RNAScope independently Position Requirements: Bachelors degree in scientific field preferred Tech-savvy, fast learner. We use a proprietary, digital LIMS system Strong verbal and written communication skills HTL or QIHC licenses, a plus Experience working at a biotech preferred

Conduct experiments to map cellular architecture in a wide range of tissue samples with our novel multi-omics spatial profiling platform. Contribute to the development and standardization of new SOPs for novel tissues and new omics chemistries. Design and conduct studies to optimize the performance and throughput of our spatial multi-omics platform. Organize and communicate data with internal and external groups. Assist in laboratory duties, including reagent preparation, instrument and inventory maintenance, and implementation of 5S practices. Responsibilities * Conduct experiments to map cellular architecture in various tissue samples using our multi-omics spatial profiling platform. * Develop and standardize new SOPs for novel tissues and omics chemistries. * Design and conduct studies to optimize the performance and throughput of our spatial multi-omics platform. * Organize and communicate data with internal and external groups. * Assist in laboratory duties, including reagent preparation, instrument and inventory maintenance, and implementation of 5S practices. Additional Skills & Qualifications * B.S. or M.S. in molecular biology, biochemistry, genetics, or related field with 1-3 years of industry experience. * Experience in tissue processing, histological slide preparation, and immunohistochemical and immunofluorescent staining in mammalian tissues. * Knowledge of a broad range of cellular, functional, IHC and/or pathology applications and imaging instrumentation. * Deep experience with molecular biology and microscopy techniques including qPCR and NGS library preparation. * Excellent communication skills, adaptive in interfacing between biologists, engineers, and other disciplines. * Ability to work full-time, on-site in New Haven, CT. Work Environment This position is based in a laboratory setting, working from 9am to 5pm on-site in New Haven, CT. The role involves collaborating closely with a multidisciplinary team of biologists, chemists, physicists, computer scientists, and engineers. Pay and Benefits The pay range for this position is $24.00 - $38.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in New Haven,CT. Application Deadline This position is anticipated to close on May 9, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Postdoctoral AssociateRequired Qualifications:Doctoral Degree (or foreign equivalent) in Cancer biology, Molecular and Cell Biology, Immunology or a closely related field degree in hand by the start of the appointment. Have one first authored publication in a highly regarded peer-reviewed journal in the field. Preferred Qualifications:The ideal candidate has laboratory research experience in cancer biology, genetic engineered mouse models, microscopy, histology, flow cytometry and/or bioinformatics. The applicant must have good problem solving and organizational skills and demonstrate the ability to conduct experiments independently and under supervision. Brief Description of Duties:The Postdoctoral Associate will assist the Principal Investigator Dr. Mario Shields in the department of PathologyThe Shields laboratory investigates the mechanisms of development and progression of diseases impacting the exocrine pancreas, such as pancreatitis and pancreatic cancer. Chronic pancreatitis is a major risk factor for pancreatic cancer, which is one of the most aggressive malignancies and among the highest mortality rate of all cancers. Current projects in the lab are focused on investigating the roles of a G-protein signaling and cell polarity in pancreatic cancer and pancreatitis. Our lab previously demonstrated that pancreas-specific deletion of the G-protein, Ga13, promotes tumor development in a genetic mouse model of pancreatic cancer. Our ongoing studies aim to define the mechanisms by which Ga13 regulates tumor metabolism and inflammation. The incumbent will conduct research and ensure that all experiments are appropriately conducted following the policies and procedures of Stony Brook University. Within the predetermined research scope and methodology, plan and conduct research● Collect and analyze data, including periodical/literature search and utilizing specialized skills in related field to analyze the collected data. ● Participate/assist in manuscript writing for publication in scientific journals and/or presentations. May also assist in grant writing. ● Assist with training and oversight of junior scientists● Lab maintenance, including equipment maintenance and ordering of supplies as needed. ● Other duties as assigned, which may include attending Scientific Conferences and Meetings. Special Notes:The Research Foundation of SUNY is a private educational corporation. Employment is subject to the Research Foundation policies and procedures, sponsor guidelines and the availability of funding. FLSA Exempt position, not eligible for the overtime provisions of the FLSA. Minimum salary threshold must be met to maintain FLSA exemption. Visit The Office of Postdoctoral Affairs to learn more about our postdoctoral community. Resume/CV and cover letter should be included with the online application. Stony Brook University is committed to excellence in diversity and the creation of an inclusive learning, and working environment. All qualified applicants will receive consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, familial status, sexual orientation, gender identity or expression, age, disability, genetic information, veteran status and all other protected classes under federal or state laws. If you need a disability-related accommodation, please call the university Office of Equity and Access (OEA) at ************** or visit OEA. In accordance with the Title II Crime Awareness and Security Act a copy of our crime statistics can be viewed here. Visit our WHY WORK HERE page to learn about the total rewards we offer. SUNY Research Foundation: A Great Place to Work. The starting salary range (or hiring range) to be offered for this position is noted below, it represents SBU's good faith and reasonable estimate of the range of possible compensation at the time of posting. Job Number: 2504480Official Job Title: Postdoctoral AssociateJob Field: Post DoctoralPrimary Location: US-NY-Stony BrookDepartment/Hiring Area: PathologySchedule: Full-time Shift :Day Shift Shift Hours: 8:30 am - 5:00pm Posting Start Date: Dec 2, 2025Posting End Date: Jan 2, 2026, 4:59:00 AMSalary:$50,000-$65,000Appointment Type: RegularSalary Grade:E89SBU Area:The Research Foundation for The State University of New York at Stony Brook

Postdoctoral AssociateRequired Qualifications:Doctoral Degree (or foreign equivalent) in Cancer biology, Molecular and Cell Biology, Immunology or a closely related field degree in hand by the start of the appointment. Have one first authored publication in a highly regarded peer-reviewed journal in the field. Preferred Qualifications:The ideal candidate has laboratory research experience in cancer biology, genetic engineered mouse models, microscopy, histology, flow cytometry and/or bioinformatics. The applicant must have good problem solving and organizational skills and demonstrate the ability to conduct experiments independently and under supervision. Brief Description of Duties:The Postdoctoral Associate will assist the Principal Investigator Dr. Mario Shields in the department of PathologyThe Shields laboratory investigates the mechanisms of development and progression of diseases impacting the exocrine pancreas, such as pancreatitis and pancreatic cancer. Chronic pancreatitis is a major risk factor for pancreatic cancer, which is one of the most aggressive malignancies and among the highest mortality rate of all cancers. Current projects in the lab are focused on investigating the roles of a G-protein signaling and cell polarity in pancreatic cancer and pancreatitis. Our lab previously demonstrated that pancreas-specific deletion of the G-protein, Ga13, promotes tumor development in a genetic mouse model of pancreatic cancer. Our ongoing studies aim to define the mechanisms by which Ga13 regulates tumor metabolism and inflammation. The incumbent will conduct research and ensure that all experiments are appropriately conducted following the policies and procedures of Stony Brook University. Within the predetermined research scope and methodology, plan and conduct research● Collect and analyze data, including periodical/literature search and utilizing specialized skills in related field to analyze the collected data. ● Participate/assist in manuscript writing for publication in scientific journals and/or presentations. May also assist in grant writing. ● Assist with training and oversight of junior scientists● Lab maintenance, including equipment maintenance and ordering of supplies as needed. ● Other duties as assigned, which may include attending Scientific Conferences and Meetings. Special Notes:The Research Foundation of SUNY is a private educational corporation. Employment is subject to the Research Foundation policies and procedures, sponsor guidelines and the availability of funding. FLSA Exempt position, not eligible for the overtime provisions of the FLSA. Minimum salary threshold must be met to maintain FLSA exemption. Visit The Office of Postdoctoral Affairs to learn more about our postdoctoral community. Resume/CV and cover letter should be included with the online application. Stony Brook University is committed to excellence in diversity and the creation of an inclusive learning, and working environment. All qualified applicants will receive consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, familial status, sexual orientation, gender identity or expression, age, disability, genetic information, veteran status and all other protected classes under federal or state laws. If you need a disability-related accommodation, please call the university Office of Equity and Access (OEA) at ************** or visit OEA. In accordance with the Title II Crime Awareness and Security Act a copy of our crime statistics can be viewed here. Visit our WHY WORK HERE page to learn about the total rewards we offer. SUNY Research Foundation: A Great Place to Work. The starting salary range (or hiring range) to be offered for this position is noted below, it represents SBU's good faith and reasonable estimate of the range of possible compensation at the time of posting. Job Number: 2504480Official Job Title: Postdoctoral AssociateJob Field: Post DoctoralPrimary Location: US-NY-Stony BrookDepartment/Hiring Area: PathologySchedule: Full-time Shift :Day Shift Shift Hours: 8:30 am - 5:00pm Posting Start Date: Dec 2, 2025Posting End Date: Jan 2, 2026, 4:59:00 AMSalary:$50,000-$65,000Appointment Type: RegularSalary Grade:E89SBU Area:The Research Foundation for The State University of New York at Stony Brook

**Introduction** Research Scientists at IBM drive the leading edge of quantum computing technologies with the industry's most advanced hardware and software. Join an elite team of researchers and engineers building a path towards scalable fault tolerant quantum computation. **Your role and responsibilities** IBM Quantum is hiring a Research Scientist to contribute to the development of advanced, high-performance digital and mixed-signal ASICs in advanced nodes for exploratory applications. We focus on circuit designs targeting the development of differentiated solutions for a range of communication and computation challenges, including the creation of CMOS-based electronics for quantum computing applications. Successful applicants will have demonstrated experience in CMOS digital integrated circuit design, including logic design, logic synthesis, and verification. In this role, you may be tasked with developing RTL, performing logic synthesis, developing testbenches, and/or integration of designs incorporating digital and analog macros. You will be involved in all aspects of design projects from concept and IC architecture exploration / definition to system integration to bring up and test; demonstrated hands-on lab skills are therefore important. In addition, background in communication theory, digital signal processing, and / or custom accelerator design would be advantageous. **Required technical and professional expertise** Degree: Master's degree or equivalent experience. - Digital Circuit Design: A strong foundation in digital design, including using EDA tools for digital logic synthesis, floor planning, place-and-route, and static timing analysis. (2 years). - CMOS implementation: Demonstrated expertise through successful implementation digital and/or mixed-signal designs in deep submicron CMOS technology (2 years). - EDA: A thorough knowledge of at least one commercial EDA digital IC design framework (2 years). **Preferred technical and professional experience** Degree: Doctorate. - Custom and/or standard cell-based digital circuit design: Proficiency in custom and/or standard cell-based digital circuit design and implementation in deep submicron technology (2 years). - Design Integration: Chip integration experience leveraging mixed-signal analog-on-top (AoT) or digital-on-top (DoT) flows. - Digital signal processing and/or accelerator design: Experience in the design, implementation, and demonstration of digital signal processing algorithms and/or custom accelerators in integrated CMOS technologies. - Programming Skills: Candidates with strong programming skills in commonly used languages (2 years). - Communication and collaboration skills: Excellent verbal and written communication skills are highly valued for effective collaboration within the team. A track record of successful participation in multi-disciplinary research and development projects is a plus. IBM is committed to creating a diverse environment and is proud to be an equal-opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender, gender identity or expression, sexual orientation, national origin, caste, genetics, pregnancy, disability, neurodivergence, age, veteran status, or other characteristics. IBM is also committed to compliance with all fair employment practices regarding citizenship and immigration status.

About the Role & Program The ESPN Research team is part of the Finance, Strategy and Research organization. The team utilizes all facets of media research (Nielsen, Adobe Analytics, Comscore/Shareablee, etc.) and primary research to inform the company about how the sports category, sports fandom, and specific sports content is performing, and how ESPN can drive even greater consumption in the future. The dates of this internship are June 8, 2026 - August 14, 2026, located in ESPN's headquarters in Bristol, CT. What You Will Do As an intern, you will participate in the collection, analysis, and communication of audience data for ESPN's linear, digital, streaming, and social media properties. The focus for this internship will be digital and social sports, both on ESPN.com, ESPN App and ESPN Social platforms. The intern will be charged with providing actionable insights to ESPN's Digital, Social & Streaming Content department, Corporate Strategy, Marketing, and other core constituents. Responsibilities include: Using Comscore/Shareablee software to query data for digital/social properties and programs Aiding in data analysis for ESPN and competitive content across ESPN digital, social, and streaming Working on research projects, including team/player social analysis, social listening, and fan community activities covering ESPN sports properties Required Qualifications & Skills Experience using Microsoft Office with a strong emphasis in Microsoft Excel and PowerPoint Comfortable working with data and high attention to detail Eager to learn new tools and data organization processes Strong interest in television content and the media landscape Preferred Qualifications & Skills Demonstrated knowledge of sports and the sports media landscape Previous experience in media and entertainment (academic or internship) Education Junior or Senior year preferred Major or previous coursework in Business Administration, Finance or related major preferred Eligibility Requirements & Program Information Candidates for this opportunity MUST meet all of the below requirements: Be enrolled in an accredited college/university pursuing a degree taking at least one class at time of application OR currently participating in a Disney College Program or Disney Internship Current Disney Interns, College, International, or Culinary Program Participants: You may only work for ONE consecutive year (12 months) in any combination of an internship and/or program Be at least 18 years of age Possess unrestricted work authorization Additional Information Able to have a consistent, reliable work schedule throughout the internship Fully available Monday through Friday for the duration of the internship, 40 hours each week Able to provide own housing for the duration of the internship program in the Bristol, CT area Able to provide/have reliable transportation to/from work The pay rate for this role in Connecticut is $22.50 per hour. Select benefits may be provided as part of the compensation package, such as medical, financial, and/or other benefits, dependent on the level and position offered. To learn more about our benefits visit: **************************************** Job Posting Segment: DO NOT USE - Production, Remote Events & Audio Job Posting Primary Business: Sports Studio & Entertainment Primary Job Posting Category: Production Intern Employment Type: Full time Primary City, State, Region, Postal Code: Bristol, CT, USA Alternate City, State, Region, Postal Code: Date Posted: 2025-12-01

ARGA Investment Management, LP seeks motivated professionals excited by global business analysis. You will develop insights into how businesses work and their normalized earnings power. You are brilliant and enjoy multicultural interaction and teamwork. Members of our research team typically cover sectors globally. This role would provide that opportunity, along with emphasis on China or Japan. We are seeking uniquely talented and entrepreneurial candidates who can help develop future offices in Asia. JOB DESCRIPTION * Understand key drivers at company and industry levels * Build detailed global industry models and forecasts * Forecast company financial statements by business segment * Identify issues and conduct company management meetings * Present conclusions through models, written reports and presentations QUALIFICATIONS * Demonstrated academic excellence in a top graduate program * Excellent oral/written communication in Mandarin Chinese or Japanese * Unquestionable integrity * Strong financial statement analysis and modeling background * Ability to understand and forecast business fundamentals * Entrepreneurial * Flexibility in international travel (at an appropriate time) Send your resume to ********************** FIRM DESCRIPTION ARGA Investment Management is a leading global value manager. ARGA manages global equity portfolios on behalf of institutional clients. We use a sophisticated process combining research and technology to identify businesses that are underpriced. ARGA is based in Stamford, CT, with offices in Chennai and Mumbai, India, Hongkong and London, UK. For more information, visit

About Us Bexorg is a cutting-edge biotech startup focused on CNS drug discovery, leveraging its proprietary BrainEx platform to conduct preclinical studies on human and porcine brains. We combine advanced wet-lab experiments with AI/ML-driven drug discovery through our XO Digital platform to revolutionize the understanding and treatment of brain disorders. We are seeking a Computational Biologist to develop and optimize computational pipelines to process and analyze complex, multi-modal datasets. You will play a critical role in extracting actionable insights from our proprietary datasets and enable downstream AI models to more accurately capture human brain complexity. Essential Duties/Tasks: ● Data Integration & Pipeline Development: Design, implement, and optimize computational pipelines for processing high-throughput, multi-modal biological data. ● Multi-Modal Analysis: Integrate diverse datasets to produce spatially and temporally resolved profiles of brain biology. ● Collaborative Research: Work closely with experimental biologists, engineers, to translate data findings into actionable insights for drug discovery and development ● Statistical & Machine Learning Methods: Develop and apply statistical models and machine learning approaches to interrogate and visualize complex biological data. ● Quality Control & Scalability: Ensure robust data quality, reproducibility, and scalability across large datasets. ● Scientific Communication: Present research findings in internal meetings, conferences, and contribute to peer-reviewed publications. Qualifications: ● PhD in Bioinformatics, Computational Biology, or a related field with clearly relevant computational projects ● Demonstrated experience with multi-omics data analysis, ideally within a neurological or biomedical context. ● Experience with RNAseq technologies, including sc/sn RNAseq ● Proficiency in programming languages such as Python and R, with hands-on experience using standard bioinformatics tools. ● Strong background in developing scalable computational workflows and data integration strategies. ● Experience with high-performance computing or cloud-based data processing. ● Excellent problem-solving skills, with the ability to work collaboratively in a multidisciplinary environment. Preferred Qualifications: ● Prior work in neurobiology or neurological disease research. ● A strong publication record in peer-reviewed scientific journals. ● Familiarity with advanced visualization techniques and data management best practices. What We Offer: ● Opportunity to work at the forefront of neuroscience and drug discovery. ● Collaborative work environment with a multidisciplinary team. ● Competitive compensation package including stock options. ● Career growth opportunities in a rapidly scaling company.

A global leader in food and beverage is interviewing for a contract Research and Development Scientist position in Valhalla, NY. The incumbent will conduct and support ingredient application programs. Qualifications: BS/MS Food Science & Technology / Food Chemistry or related field • 3-5 years of experience in the Food Industry or related area • Understanding of food chemistry, carbohydrates, product formulation and development, ingredient technology, and food safety • Functional knowledge of analytical test methodologies and data interpretation • Ability to make significant technical, and scientific advances utilizing internal and/or external resources. • Detail-oriented individual with proven ability to independently lead multiple projects and work streams simultaneously, leveraging project management tools. • Self-starter with good oral and written communication and presentation skills, the ability to work with various personalities and work styles, • Ability to travel when needed

The Nassau-Suffolk Hospital Council (NSHC) is seeking a paid temporary part-time intern to join our team. Reporting to the Manager of Communications, Health Outreach, and Research, this position provides communications activities in support of the Long Island Health Collaborative (LIHC), the Suburban Hospital Alliance of New York State (SHANYS), and SHANYS' regional organizations: the Nassau-Suffolk Hospital Council (NSHC, Long Island region) and the Northern Metropolitan Hospital Association (NorMet, Hudson Valley region). This position is hybrid, with some time working remotely and some time working in the NSHC office, located at 800 Veterans Memorial Highway, Suite 150 in Hauppauge, NY. Remote and in-person work schedule to be determined based on intern's availability. Candidates must be enrolled in a bachelor's degree program pertaining to communications, public relations, health communications, or another relevant area of study. Compensation, Hours & Length of Internship Compensation: $19/hour 8 hours per week, weekly schedule to be determined based on candidate's availability 14 total weeks Primary Role Assists Manager of Communications, Health Outreach, and Research with communications activities primarily in support of New York Coalition for Transportation Safety (NYCTS) grant deliverables. Also assists with communications activities in support of the Long Island Health Collaborative (LIHC), the Suburban Hospital Alliance of New York State (SHANYS), Nassau-Suffolk Hospital Council (NSHC), and Northern Metropolitan Hospital Association (NorMet) as needed. Key Responsibilities Communications & Outreach Attend meetings with Manager of Communications, Health Outreach, and Research Assist with development and creation of communications materials on behalf of NSHC, NorMet, the LIHC, and NYCTS grant activities, including but not limited to social media campaigns and posts; blog posts; press releases; letters to various audiences such as media, the community, and members; thematic reports; webpage content; and other content as needed. Assist with graphic design of communications materials via Canva including but not limited to social media graphics; postcards; flyers; and infographics. Contact individuals, community-based organizations, and NSHC/NorMet/LIHC members as needed. Assist with distribution of Community Health Assessment Survey (CHAS). Research Research new contact lists and update existing lists including but not limited to physicians; libraries; elementary, middle, and high schools; legislators; media; and community-based organizations. Research of topics including but not limited to population health; census data; statistics for grant-writing; upcoming local events; NSHC/NorMet/LIHC member news; and more. Data Entry and Reports Enter paper-based CHAS and NYCTS into SurveyMonkey analysis platform Create and export reports from SurveyMonkey Create custom data reports as needed Events Assist with coordination and promotion of community outreach events Attend all virtual and in-person events, when candidate's schedule allows Assists with survey distribution and collection at in-person events Special Projects Depending on intern's unique skillsets, other specialized projects related to communications, outreach, and research may be assigned Other relevant duties as assigned Qualifications Candidate must be enrolled in a bachelor's degree program pertaining to communications, public relations, health communications, or another relevant area of study Must have excellent communication skills, especially writing skills Computer literate, especially in Microsoft Office suite of functions Proficiency in Survey Monkey a plus Proficiency in Canva a plus Interest and knowledge of healthcare, public health, New York's healthcare landscape, data analytics, and/or health policy a plus

The Clinical Development Operations fellowship is designed to provide the PharmD fellow with an understanding of the history of drug development and how the US Code of Federal Regulations and International Conference on Harmonization (ICH) - Good Clinical Practice (GCP) set the framework under which clinical trials are conducted. To facilitate hands-on training, the fellow will be assigned to work on one or more clinical trials under the supervision of an experienced Clinical Trial Manager (CTM) and/or Clinical Trial Leader (CTL). The CTM/CTL will be responsible for guiding and mentoring the fellow on the strategic and operational aspects of his/her assigned clinical trials. There may also be an opportunity for the fellow to undertake special projects. Through direct mentoring and rotations, the fellow will gain an understanding of the broad range of career opportunities available to a pharmacist in Clinical Development Operations. Although the fellow will be based in Study Management & Conduct, he/she will have an opportunity to rotate/shadow through other departments within the broader Medical Department as appropriate. The intention of these rotations is to increase the fellow's understanding of how the work of specialized functions is critical the overall conduct of clinical trials. As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility, and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees. **Duties & Responsibilities** **Trial Preparation, Conduct, and Closeout:** + Select sites for study conduct and deliver the trial according to the clinical trial protocol, within trial timelines, and in compliance with ICH-GCP and all other relevant external regulations + Lead and support local trial team and investigative sites in timely preparation of required trial documents, contracts and necessary approvals + All Regulatory Requirements are satisfied prior to trial/site initiation + Where necessary, set up and manage external suppliers that meet requirements of local/regional trial operations + Set up, manage and review operating unit (OPU) trial budget to ensure appropriate level of financial oversight. Timely budget updates based on trial changes + Ensure appropriate trial-specific training of OPU internal and external partners in line with Trial Training Plan + In collaboration with Site Monitoring Lead and Clinical Research Associates (CRAs), ensure provision of appropriate trial oversight for the trials by monitoring compliance of trial sites and BI team to GCP, local regulations, BI Standard Operating Procedures (SOPs) (for BI staff and issue), and adherence to trial protocol, adequate trial supply distribution to sites + Continuous and timely data entry and cleaning, and on time Data Base Lock (DBL) + Trial contact for CRAs, investigators and site staff + In collaboration with Trial Resource Specialist and with support from CRAs as appropriate, ensures collection of required documents, with timely, complete and compliant archiving of all relevant documents for the electronic Trial Master File (eTMF) and Clinical Trial Report (CTR) Appendices **Management and Relationship Responsibilities:** + Develop and maintain company relationships with external experts and investigational sites by coordinating and ensuring cross-functional collaboration amongst Clinical Operations and Medical Affairs on Regional/ local level, and supporting CRAs in site contacts + Collaborates with other BI functions to support Trial Management topics and support integration across Medicine + Participate in working groups related to Trial Management, represent trial on local and regional level, providing updates on trial within R/OPU **Application Requirements** **1. Curriculum vitae** **2. Letter of intent** - focusing on how a fellowship at Boehringer Ingelheim can help further your career growth. ***** Please upload under My Documents, Additional Attachments. **Requirements** + Doctor of Pharmacy degree from an ACPE-accredited school or college of pharmacy earned prior to the start date at Boehringer Ingelheim OR Ph.D. degree in related discipline + **PharmD candidates preferred. + Highly motivated and shows initiative in contributing to team deliverables + Receptive to receiving and quickly implementing constructive feedback + Ability to work independently within provided guidance from team leads + Adaptable and able to contribute to multiple Therapeutic Areas as needed + Excellent verbal and written communication skills + Proven experience working in a dynamic, high-volume environment handling multiple tasks + Strong computer skills, including Outlook, Word, PowerPoint, and Excel + Foundational understanding of corporate structure, regulatory considerations and the drug development process in pharmacy with an ability to quickly adapt to a changing corporate environment that will allow the incumbent to be productive in rotational experiences **Desired Skills, Experience and Abilities** Prior pharmaceutical industry experience (e.g. internship or Advanced Pharmacy Practice Experience [APPE] rotation is preferred but not required.) **Compensation** Compensation: This position offers a base salary of $80,000. The position may be eligible for a role specific variable or performance based bonus and or other compensation elements. For an overview of our benefits please click here. (***************************************************************** All qualified applicants will receive consideration for employment without regard to a person's actual or perceived race, including natural hairstyles, hair texture and protective hairstyles; color; creed; religion; national origin; age; ancestry; citizenship status, marital status; gender, gender identity or expression; sexual orientation, mental, physical or intellectual disability, veteran status; pregnancy, childbirth or related medical condition; genetic information (including the refusal to submit to genetic testing) or any other class or characteristic protected by applicable law.

NYMC is seeking a Postdoctoral Fellow for the Department of Cell Biology and Anatomy. The position is available in the El Ouaamari laboratory to investigate the role of the peripheral neurons in the regulation of systemic energy homeostasis. Self-driven, creative, resourceful and independent candidates with a PhD in neuroscience and/or endocrine physiology are encouraged to apply. Successful applicants will develop a research project focused on understanding how peripheral neurons control glucose and lipid homeostasis with the long-term goal of identifying high-value biological data that can be harnessed to design neuromodulation-based strategies to counter diabetes and/or obesity. The successful candidate will contribute to the training of research assistants and graduate students and actively participate in lab and departmental meetings. How to apply: Interested candidates should submit a complete CV, a summary of current and future research interests, and the contact information of three references to Dr. Abdelfattah El Ouaamari, Ph.D. at *****************. Compensation: Salary will be determined based on the experience of the candidate and the NYMC guidelines. Responsibilities To perform in vitro and in vivo experiments in mouse models of diabetes and obesity. To analyze and interpret data. To write and publish articles in peer-reviewed journals. To train research assistants and graduate students. To actively participate in lab and departmental scientific meeting. Qualifications Education requirement: PhD in neuroscience and/or endocrine physiology or related. Other skills/requirements: The candidate must have prior experience in (1) animal physiology, (2) molecular biology, (3) histology and imaging, and (4) primary cell culture. Preference will be given to candidates who are familiar with in vitro and in vivo techniques for manipulating and monitoring neuronal activity. Minimum Salary USD $44,505.60/Yr. Maximum Salary USD $55,632.00/Yr.

Introduction Research Scientists at IBM drive the leading edge of quantum computing technologies with the industry's most advanced hardware and software. Join an elite team of researchers and engineers building a path towards scalable fault tolerant quantum computation. Your role and responsibilities IBM Quantum is hiring a Research Scientist to contribute to the development of advanced, high-performance digital and mixed-signal ASICs in advanced nodes for exploratory applications. We focus on circuit designs targeting the development of differentiated solutions for a range of communication and computation challenges, including the creation of CMOS-based electronics for quantum computing applications. Successful applicants will have demonstrated experience in CMOS digital integrated circuit design, including logic design, logic synthesis, and verification. In this role, you may be tasked with developing RTL, performing logic synthesis, developing testbenches, and/or integration of designs incorporating digital and analog macros. You will be involved in all aspects of design projects from concept and IC architecture exploration / definition to system integration to bring up and test; demonstrated hands-on lab skills are therefore important. In addition, background in communication theory, digital signal processing, and / or custom accelerator design would be advantageous. Required education Master's Degree Preferred education Doctorate Degree Required technical and professional expertise Degree: Master's degree or equivalent experience. * Digital Circuit Design: A strong foundation in digital design, including using EDA tools for digital logic synthesis, floor planning, place-and-route, and static timing analysis. (2 years). * CMOS implementation: Demonstrated expertise through successful implementation digital and/or mixed-signal designs in deep submicron CMOS technology (2 years). * EDA: A thorough knowledge of at least one commercial EDA digital IC design framework (2 years). Preferred technical and professional experience Degree: Doctorate. * Custom and/or standard cell-based digital circuit design: Proficiency in custom and/or standard cell-based digital circuit design and implementation in deep submicron technology (2 years). * Design Integration: Chip integration experience leveraging mixed-signal analog-on-top (AoT) or digital-on-top (DoT) flows. * Digital signal processing and/or accelerator design: Experience in the design, implementation, and demonstration of digital signal processing algorithms and/or custom accelerators in integrated CMOS technologies. * Programming Skills: Candidates with strong programming skills in commonly used languages (2 years). * Communication and collaboration skills: Excellent verbal and written communication skills are highly valued for effective collaboration within the team. A track record of successful participation in multi-disciplinary research and development projects is a plus. ABOUT BUSINESS UNIT IBM Research is the organic growth engine of IBM and an innovation engine for our customers and partners. As part of this mission, IBM Research anticipates and examines 'What's Next in Computing' to ultimately create and integrate the technologies the world relies upon to solve big challenges and unlock new opportunities. We create and pioneer new markets for IBM, our partners and customers as exemplified in our ongoing quest to reach practical and large-scale quantum computing. Across IBM Research, we realize the power and potential to accelerate discovery with our partners and clients by combining the power of high performance computing, AI, and Quantum, all integrated through the hybrid cloud. YOUR LIFE @ IBM In a world where technology never stands still, we understand that, dedication to our clients success, innovation that matters, and trust and personal responsibility in all our relationships, lives in what we do as IBMers as we strive to be the catalyst that makes the world work better. Being an IBMer means you'll be able to learn and develop yourself and your career, you'll be encouraged to be courageous and experiment everyday, all whilst having continuous trust and support in an environment where everyone can thrive whatever their personal or professional background. Our IBMers are growth minded, always staying curious, open to feedback and learning new information and skills to constantly transform themselves and our company. They are trusted to provide on-going feedback to help other IBMers grow, as well as collaborate with colleagues keeping in mind a team focused approach to include different perspectives to drive exceptional outcomes for our customers. The courage our IBMers have to make critical decisions everyday is essential to IBM becoming the catalyst for progress, always embracing challenges with resources they have to hand, a can-do attitude and always striving for an outcome focused approach within everything that they do. Are you ready to be an IBMer? ABOUT IBM IBM's greatest invention is the IBMer. We believe that through the application of intelligence, reason and science, we can improve business, society and the human condition, bringing the power of an open hybrid cloud and AI strategy to life for our clients and partners around the world. Restlessly reinventing since 1911, we are not only one of the largest corporate organizations in the world, we're also one of the biggest technology and consulting employers, with many of the Fortune 500 companies relying on the IBM Cloud to run their business. At IBM, we pride ourselves on being an early adopter of artificial intelligence, quantum computing and blockchain. Now it's time for you to join us on our journey to being a responsible technology innovator and a force for good in the world. IBM is proud to be an equal-opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender, gender identity or expression, sexual orientation, national origin, genetics, pregnancy, disability, neurodivergence, age, or other characteristics protected by the applicable law. IBM is also committed to compliance with all fair employment practices regarding citizenship and immigration status. OTHER RELEVANT JOB DETAILS IBM offers a competitive and comprehensive benefits program. Eligible employees may have access to: * Healthcare benefits including medical & prescription drug coverage, dental, vision, and mental health & well being * Financial programs such as 401(k), cash balance pension plan, the IBM Employee Stock Purchase Plan, financial counseling, life insurance, short & long- term disability coverage, and opportunities for performance based salary incentive programs * Generous paid time off including 12 holidays, minimum 56 hours sick time, 120 hours vacation, 12 weeks parental bonding leave in accordance with IBM Policy, and other Paid Care Leave programs. IBM also offers paid family leave benefits to eligible employees where required by applicable law * Training and educational resources on our personalized, AI-driven learning platform where IBMers can grow skills and obtain industry-recognized certifications to achieve their career goals * Diverse and inclusive employee resource groups, giving & volunteer opportunities, and discounts on retail products, services & experiences We consider qualified applicants with criminal histories, consistent with applicable law. This position was posted on the date cited in the key job details section and is anticipated to remain posted for 21 days from this date or less if not needed to fill the role. IBM will not be providing visa sponsorship for this position now or in the future. Therefore, in order to be considered for this position, you must have the ability to work without a need for current or future visa sponsorship. The compensation range and benefits for this position are based on a full-time schedule for a full calendar year. The salary will vary depending on your job-related skills, experience and location. Pay increment and frequency of pay will be in accordance with employment classification and applicable laws. For part time roles, your compensation and benefits will be adjusted to reflect your hours. Benefits may be pro-rated for those who start working during the calendar year.

ARGA Investment Management, LP seeks motivated professionals excited by global business analysis. You will develop insights into how businesses work and their normalized earnings power. You are brilliant and enjoy multicultural interaction and teamwork. Members of our research team typically cover sectors globally. JOB DESCRIPTION * Understand key drivers at company and industry levels * Build detailed global industry models and forecasts * Forecast company financial statements by business segment * Identify issues and conduct company management meetings * Present conclusions through models, written reports and presentations QUALIFICATIONS * Demonstrated academic excellence in a top graduate program * Excellent oral/written communication * Unquestionable integrity * Strong financial statement analysis and modeling background * Ability to understand and forecast business fundamentals * Entrepreneurial * Flexibility in international travel (at an appropriate time) Send your resume to ********************** FIRM DESCRIPTION ARGA Investment Management is a leading global value manager. ARGA manages global equity portfolios on behalf of institutional clients. We use a sophisticated process combining research and technology to identify businesses that are underpriced. ARGA is based in Stamford, CT, with offices in Chennai and Mumbai, India, Hongkong and London, UK. For more information, visit