Clinical Research Coordinator Jobs in Modesto, CA

PRIDE Health is seeking a travel Clinical Research Coordinator for a travel job in Los Angeles, California. Job Description & Requirements Specialty: Clinical Research Coordinator Discipline: Allied Health Professional Start Date: 04/07/2025 Duration: 13 weeks 40 hours per week Shift: 8 hours, days Employment Type: Travel Pride Health Job ID #16108617. Pay package is based on 8 hour shifts and 40.0 hours per week (subject to confirmation) with tax-free stipend amount to be determined. Posted job title: Clinical Research:Clinical Research Coordinator,09:00:00-17:00:00 About PRIDE Health PRIDE Health is the minority-owned healthcare recruitment division of Pride Global-an integrated human capital solutions and advisory firm. With our robust and abundant travel nursing and allied health employment options across the U.S., PRIDE Health will allow you to help change the way the world lives and heals as it connects you with the industry's leading healthcare organizations. Pride Global offers eligible employee's comprehensive healthcare coverage (medical, dental, and vision plans), supplemental coverage (accident insurance, critical illness insurance and hospital indemnity), 401(k)-retirement savings, life & disability insurance, an employee assistance program, legal support, auto, home insurance, pet insurance, and employee discounts with preferred vendors. Benefits Weekly pay Holiday Pay Guaranteed Hours 401k retirement plan Cancelation protection Referral bonus Medical benefits Dental benefits Vision benefits

Title: Clinical Trial Coordinator Contract to Hire: 6-month contract Responsibilities: Assist in operational and administrative research support under the clinical direction of the Principal Investigator (PI) Ensure compliance with institutional, federal, and sponsor regulations (e.g., FDA, IRB) Maintain accurate and up-to-date regulatory documents and study records Obtain informed consent from study participants under investigator supervision. Schedule and coordinate participant visits and follow-ups. Requirements: High School Diploma ~1 year of experience working in clinical trials Strong Organizational and Communication skills Ability to work effectively on cross-functional teams Prior experience in a Clinical Trials setting is highly preferred

Tata Elxsi brings together the best technology and user-centric design expertise to help customers deliver innovative solutions and great consumer experiences. Our integrated Design and Technology teams help enterprises reimagine their products and services - from strategy, consumer research and insights, to service and experience design, technology implementation, integration, launch, and beyond. We are looking for an experienced In-Person Moderator with a strong background in data collection, photography, and videography. This role will involve moderating participants and collecting high-quality images and videos at various residential locations across multiple cities. This is a field-based, temporary contract position that requires travel within the USA. Key Responsibilities: Data Collection & Quality Assurance: • Capture and document high-quality images and videos, ensuring they meet study guidelines and protocol. • Review and validate collected data on-site, ensuring clarity, accuracy, and proper documentation before uploading. • Organize and label all data files according to project specifications. In-Person Moderation: • Lead participant onboarding, providing clear instructions about the study and expectations for data collection. • Ensure that all participants follow the data collection protocol and address any questions or concerns during the process. • Maintain positive and professional communication with participants throughout the study. Adept at prioritizing research activities to deliver practical insights and direction quickly Understand the needs, challenges during the moderation and mitigate the same Site Preparation & Setup: • Set up and test data collection equipment (e.g., cameras, tablets, mobile devices) at each site before sessions begin. • Ensure all equipment is functioning properly and address any technical issues on-site. Logistics & Travel: • Travel between data collection sites across the USA, arriving on time and fully prepared for each session. • Organize logistics to ensure smooth transitions between sites, including necessary travel arrangements and accommodation. • Remain flexible to accommodate changes in travel or collection schedules based on study needs. Equipment Management: • Safely operate and maintain data collection equipment, ensuring proper functionality. • Troubleshoot minor technical issues on-site and report any significant issues to the project manager. • Prior experience in photography or videography is required, with an understanding of camera operation, framing, lighting, and video capture. • Experience with field-based data collection • Expertise designing and executing evaluative research studies to assess digital experiences • Experience moderating in- person, remote/virtual research with research participants (e.g., interviews, usability testing) • Expertise in survey design Qualifications and Skills: Experience: • Prior experience in photography or videography is required, with an understanding of camera operation, framing, lighting, and video capture. • Experience with field-based data collection is a plus. • Experience with field-based data collection • Expertise designing and executing evaluative research studies to assess digital experiences • Experience moderating in- person, remote/virtual research with research participants (e.g., interviews, usability testing) • Expertise in survey design. Skills & Competencies: • Attention to Detail: Ability to ensure data accuracy, clarity, and adherence to project protocols. • Communication Skills: Strong interpersonal skills for moderating participants and ensuring clear communication of guidelines. • Technical Proficiency: Comfortable using various data collection tools such as cameras, tablets, and mobile devices. • Photography/Videography Skills: A demonstrated interest or experience in capturing high-quality images and videos with an understanding of technical and aesthetic standards. • Has computer trouble shooting experience, • Handling hardware and software trouble shooting • Organizational Skills: Ability to keep track of collected data and ensure everything is properly stored, labeled, and uploaded. • Problem Solving: Ability to identify and resolve minor technical and logistical issues on-site. Other Requirements: • Ability to travel and work across various US cities; occasional overnight stays may be required. • Flexible schedule with possibility of working in night shift and the ability to work 5 days a week, including potential extended hours depending on data collection needs. Tata Elxsi offers a comprehensive compensation and benefits package. Tata Elxsi is an affirmative action-equal opportunity employer. Tata Elxsi complies with all applicable federal, state and local laws regarding recruitment and hiring. All qualified applicants are considered for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, citizenship status, disability, protected veteran status, or any other category protected by applicable federal, state or local laws. Tata Elxsi does not currently require partners or employees to be fully vaccinated or test negative for COVID-19 in order to go to Tata Elxsi offices, client sites or Tata Elxsi events, except when mandated by federal, state or local law. In some circumstances, clients also may require proof of vaccination or testing (e.g., to go to the client site). What are our perks for Full time employee? We provide unique options to fit your unique lives!. Our menu of flexible options includes, but is not limited to: • Excellent healthcare options: Medical, vision, prescription & dental • Family Focus & Balance: medical, commuters & Dependent FSA, Competitive PTO, Sick Time, and Employee Assistance Program • Financial Security: Competitive 401(k) match with Safe Harbor Plan, • Employee Recognition Programs • Perks AT works: Our exclusive one-stop online discount marketplace

In this role you will ensure IRB approved protocols are implemented and followed; execute the informed consent process and monitor patient status and safety; collect and organize research data; schedule and conduct study-specific training and site in-services to study related staff on new or amended protocols, and educate patients and their families about treatments and possible side effects. The Clinical Research Coordinator must also be able to perform clinical tasks. Responsibilities: ● Site preparation. ● Obtaining informed consent, patient screening and recruitment. ● Patient enrollment, and conducting study visits. ● Maintaining and dispensing study product and supplies. ● Completing and ensuring the quality of case report forms. ● Maintaining source documents ● Ensuring site quality. ● Maintain a thorough and meticulous working knowledge of protocol schemas and ● requirements. ● Collaborate with physicians to maintain strict protocol adherence and serve as a ● resource for members of staff. ● Writes patient information sheet for clinical studies for submission to IRB, as well as ● complete the necessary documents for IRB admission in a timely fashion. ● Participate in the development and implementation of patient educational materials. ● Writes patient information sheet (ICF) for clinical studies for admission to IRB, as well as ● complete the necessary documents for IRB submission in a timely fashion. ● Review research and administrative documents to determine action items, prioritizing ● and tracking action items. ● Responsible for completion, submission and tracking of regulatory documents to the ● IRB.

About Us: How many companies can say they've been in business for over 177 years?! Here at ZEISS, we certainly can! As the pioneers of science, ZEISS handles the everchanging environments in a fast-paced world, meeting it with cutting edge of technologies and continuous advancements. ZEISS believes that innovation and technology are the key to a sustainable future and solutions for global change. We have a diverse range of portfolios throughout the ZEISS family in segments like, Industrial Quality & Research, Medical Technology, Consumer Markets and Semiconductor Manufacturing Technology. We are a global company with over 42,000 employees and have over 4,000 in the US and Canada alone! Make a difference, come join the team! Location/Region: This position is located in Dublin, CA. What's the role? As a Staff Clinical Research Scientist, you get to work with an astonishing team that plays a vital role at Carl Zeiss Meditec, Inc.. Show case your skills and experience with process enhancement [ Sound Interesting? Here's what you'll do: The Staff Clinical Research Scientist is responsible for the day-to-day management of academics under contract as well as in-house Professional Affairs staff involved in applications development. Responsible for the management of clinical research teams in practices and university settings. With the VP of Professional Affairs, interacts with ophthalmology thought leaders worldwide Manage staff in the design and execution of clinical studies for the purpose of assessing the performance of current products, of applications under development or modification, and of competitors' products. Oversee the production of analyses and reports documenting clinical studies. Manage clinical research teams in the development and evaluation of new applications for new and existing products. Supervise evaluation of application performance and the Alpha testing of new applications and products. Primary contact for R&D and Marketing departments for internal application development projects and primary contact for external clinical sites. Maintain operational competence with most Carl Zeiss Meditec product Maintain computer and statistical skills consistent with needs of position. Maintain knowledge of corporate guidelines for Good Clinical Research Practices and of IRB procedures. Do you qualify? Four-year degree or equivalent with emphasis in the Physical Sciences, Mathematics, Statistics, or Engineering. At least seven (7) years experience in clinical research and in handling subjects and patients in a clinical research setting. Ability to move smoothly and professionally in the medical environment. The annual pay range for this position is $137,300 - $171,600. The pay offered for this role may be influenced by factors such as job location, scope of role, qualifications, education, experience, & complexity/specialization/scarcity of talent. This position is eligible for a Performance Bonus. ZEISS also offers robust benefits, including medical plans, retirement savings plan and paid time off. ZEISS is an EEO/AA/M/F/Disabled Veteran Employer Your ZEISS Recruiting Team: Jo Anne Mittelman Zeiss provides Equal Employment Opportunity without unlawful regard to an Applicants race, color, religion, creed, sex, gender, marital status, age, national origin or ancestry, physical or mental disability, medical condition, military or veteran status, citizen status, sexual orientation, pregnancy (includes childbirth, breastfeeding or related medical condition), genetic predisposition, carrier status, gender expression or identity, including transgender identity, or any other class or characteristic protected by federal, state, or local law of the employee (or the people with whom the employee associates, including relatives and friends).

About Us: How many companies can say they've been in business for over 177 years?! Here at ZEISS, we certainly can! As the pioneers of science, ZEISS handles the everchanging environments in a fast-paced world, meeting it with cutting edge of technologies and continuous advancements. ZEISS believes that innovation and technology are the key to a sustainable future and solutions for global change. We have a diverse range of portfolios throughout the ZEISS family in segments like, Industrial Quality & Research, Medical Technology, Consumer Markets and Semiconductor Manufacturing Technology. We are a global company with over 42,000 employees and have over 4,000 in the US and Canada alone! Make a difference, come join the team! Location/Region: This position is located in Dublin, CA. What's the role? As a Staff Clinical Research Scientist, you get to work with an astonishing team that plays a vital role at Carl Zeiss Meditec, Inc.. Show case your skills and experience with process enhancement [ Sound Interesting? Here's what you'll do: The Staff Clinical Research Scientist is responsible for the day-to-day management of academics under contract as well as in-house Professional Affairs staff involved in applications development. Responsible for the management of clinical research teams in practices and university settings. With the VP of Professional Affairs, interacts with ophthalmology thought leaders worldwide Manage staff in the design and execution of clinical studies for the purpose of assessing the performance of current products, of applications under development or modification, and of competitors' products. Oversee the production of analyses and reports documenting clinical studies. Manage clinical research teams in the development and evaluation of new applications for new and existing products. Supervise evaluation of application performance and the Alpha testing of new applications and products. Primary contact for R&D and Marketing departments for internal application development projects and primary contact for external clinical sites. Maintain operational competence with most Carl Zeiss Meditec product Maintain computer and statistical skills consistent with needs of position. Maintain knowledge of corporate guidelines for Good Clinical Research Practices and of IRB procedures. Do you qualify? Four-year degree or equivalent with emphasis in the Physical Sciences, Mathematics, Statistics, or Engineering. At least seven (7) years experience in clinical research and in handling subjects and patients in a clinical research setting. Ability to move smoothly and professionally in the medical environment. The annual pay range for this position is $137,300 - $171,600. The pay offered for this role may be influenced by factors such as job location, scope of role, qualifications, education, experience, & complexity/specialization/scarcity of talent. This position is eligible for a Performance Bonus. ZEISS also offers robust benefits, including medical plans, retirement savings plan and paid time off. ZEISS is an EEO/AA/M/F/Disabled Veteran Employer Your ZEISS Recruiting Team: Jo Anne Mittelman Zeiss provides Equal Employment Opportunity without unlawful regard to an Applicants race, color, religion, creed, sex, gender, marital status, age, national origin or ancestry, physical or mental disability, medical condition, military or veteran status, citizen status, sexual orientation, pregnancy (includes childbirth, breastfeeding or related medical condition), genetic predisposition, carrier status, gender expression or identity, including transgender identity, or any other class or characteristic protected by federal, state, or local law of the employee (or the people with whom the employee associates, including relatives and friends).

St. Joseph's Medical Center is a member of Dignity Health. The word dignity perfectly defines what our organization stands for showing respect for all people by providing excellent care. St. Joseph's Medical Center was founded in 1899 under the direction of the Dominican Sisters of San Rafael and is a not-for-profit fully-accredited regional hospital with 395 beds a physician staff of over 400 and more than 2400 employees. Specializing in cardiovascular care comprehensive cancer services and women and children's services including neonatal intensive care St. Joseph's is the largest hospital as well as the largest private employer in Stockton California. Nationally recognized as a quality leader St. Joseph's is consistently chosen as the most preferred hospital by local consumers. One Community. One Mission. One California (********************************** QgPZ6ZWZM60TPV) **Responsibilities** The Research Coordinator will provide comprehensive administrative and operational support to the Research Director and assist in managing various resident-related activities. This role is pivotal in ensuring smooth coordination between the Research Director, residents, and program coordinators, supporting GME's scholarly and research objectives. The ideal candidate is organized, detail-oriented, and capable of handling multiple priorities in a fast paced environment. Flexibility and a willingness to take on additional responsibilities as they arise are essential for success in this role. **Job Duties:** **Administrative Support:** + Assist the Research Director with day-to-day tasks and ensure timely follow-up on pending matters. + Manage calendars and schedules, including setting up meetings with residents and other stakeholders. + Serve as the primary point of contact for residents regarding research-related inquiries and scheduling. **Coordination of Resident Activities:** + Collaborate with program coordinators to plan and organize resident-related research activities. + Maintain clear and proactive communication with all involved parties to ensure efficient coordination. **Data Management:** + Help the Research Director update and maintain scholarly trackers, ensuring accurate and up-to-date records of resident research progress. + Help the Research Director manage the research elective spreadsheet, ensuring all information is current and properly documented. **General Support:** + Perform administrative tasks and duties as assigned to support GME's research program goals. + Take on additional responsibilities or projects as they arise to meet departmental needs. **We offer the following benefits to support you and your family:** + Health/Dental/Vision Insurance + Flexible spending accounts + Voluntary Protection: Group Accident Critical Illness and Identity Theft + Adoption Assistance + Free Premium Membership to Care.com with preloaded credits for children and/or dependent adults + Employee Assistance Program (EAP) for you and your family + Paid Time Off (PTO) + Tuition Assistance for career growth and development + Retirement Programs + Wellness Programs **Qualifications** **Minimum Requirements:** **Education and Experience:** + Bachelor's degree preferred. + Prior experience in administrative support or program coordination is highly desirable. **Required minimum knowledge, skills, abilities, and training:** + Prior experience in administrative support or program coordination is highly desirable. + Excellent written and verbal communication skills. + Proficient in Excel, Word, PowerPoint and other relevant software. + Ability to work independently and collaboratively in a team setting. + Attention to detail and a commitment to accuracy. + Professional demeanor and ability to handle sensitive information confidentially. **Preferred minimum knowledge, skills, abilities, and training:** + Familiarity with research modalities and IRB preparation and workflow not required but a plus. **Pay Range** $33.60 - $48.73 /hour We are an equal opportunity/affirmative action employer.

St. Joseph's Medical Center is a member of Dignity Health. The word dignity perfectly defines what our organization stands for showing respect for all people by providing excellent care. St. Joseph's Medical Center was founded in 1899 under the direction of the Dominican Sisters of San Rafael and is a not-for-profit fully-accredited regional hospital with 395 beds a physician staff of over 400 and more than 2400 employees. Specializing in cardiovascular care comprehensive cancer services and women and children's services including neonatal intensive care St. Joseph's is the largest hospital as well as the largest private employer in Stockton California. Nationally recognized as a quality leader St. Joseph's is consistently chosen as the most preferred hospital by local consumers. One Community. One Mission. One California Responsibilities The Research Coordinator will provide comprehensive administrative and operational support to the Research Director and assist in managing various resident-related activities. This role is pivotal in ensuring smooth coordination between the Research Director, residents, and program coordinators, supporting GME's scholarly and research objectives. The ideal candidate is organized, detail-oriented, and capable of handling multiple priorities in a fast paced environment. Flexibility and a willingness to take on additional responsibilities as they arise are essential for success in this role. Job Duties: Administrative Support: Assist the Research Director with day-to-day tasks and ensure timely follow-up on pending matters. Manage calendars and schedules, including setting up meetings with residents and other stakeholders. Serve as the primary point of contact for residents regarding research-related inquiries and scheduling. Coordination of Resident Activities: Collaborate with program coordinators to plan and organize resident-related research activities. Maintain clear and proactive communication with all involved parties to ensure efficient coordination. Data Management: Help the Research Director update and maintain scholarly trackers, ensuring accurate and up-to-date records of resident research progress. Help the Research Director manage the research elective spreadsheet, ensuring all information is current and properly documented. General Support: Perform administrative tasks and duties as assigned to support GME's research program goals. Take on additional responsibilities or projects as they arise to meet departmental needs. We offer the following benefits to support you and your family: Health/Dental/Vision Insurance Flexible spending accounts Voluntary Protection: Group Accident Critical Illness and Identity Theft Adoption Assistance Free Premium Membership to Care.com with preloaded credits for children and/or dependent adults Employee Assistance Program (EAP) for you and your family Paid Time Off (PTO) Tuition Assistance for career growth and development Retirement Programs Wellness Programs Qualifications Minimum Requirements: Education and Experience: Bachelor's degree preferred. Prior experience in administrative support or program coordination is highly desirable. Required minimum knowledge, skills, abilities, and training: Prior experience in administrative support or program coordination is highly desirable. Excellent written and verbal communication skills. Proficient in Excel, Word, PowerPoint and other relevant software. Ability to work independently and collaboratively in a team setting. Attention to detail and a commitment to accuracy. Professional demeanor and ability to handle sensitive information confidentially. Preferred minimum knowledge, skills, abilities, and training: Familiarity with research modalities and IRB preparation and workflow not required but a plus.

As a Clinical Research Associate you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Responsibilities What you will be doing: * Strong written and verbal communication skills in English and local language (if applicable), good presentation, negotiation and influencing * Ability to effectively manage multiple priorities and responsibilities of increasing scope and complexity. * Strong planning & organizational skills, and the ability to work efficiently and effectively * Proactive, conscientious and precise in delivery of quality work even when under pressure * Effective at analyzing and escalating issues at the right functional level, solving problems and resolving conflicts in a timely manner * Flexible with high learning and change agility * Knowledge of local regulations, IND/ICH GCP - guidelines, * Available and willing to travel as job requires * Communicate the progress and relevant information or escalate issues of the study to the appropriate study management team * Engage and maintain good written and verbal communication with external stakeholders in order to ensure effectiveness * Accountable for local activities required in set up and for high quality execution of studies; will seek managerial or other experienced support as appropriate * Performs operational site evaluation visits, study initiation visits, on and off-site monitoring visits at the required frequency and site close-out * Determines the feasibility of the study protocol with reference to study complexity * Confirms staff availability, suitable clinical facilities, potential for per protocol patient population * Confirms ability to comply with ICH GCP and requirements for clinical studies. * Works with Study staff to carry out a local study / site level risk * Participate in global investigators and/or monitor meetings as appropriate. Facilitates investigator's participation in global meetings and/or may assist the study staff with organizing local investigator Participates in other study meetings as required. * Maintain good relationship with sites and ensure that critical study timelines related to monitoring activities are achieved and that recruitment targets, patient recruitment cycle times, data and audit quality and site related milestones are * Ensure that investigators and staff fully understand their roles and responsibilities with respect to regulatory requirements (ICH-GCP). * Work with the sites to ensure they address data queries in a timely Verifying that data entered in to the CRFs is consistent with patient medical notes and entered in real time. * Ensure Investigator and site staff receives safety reports and new safety information in a timely manner. * Ensure the accuracy of data collected for safety reporting (AEs, SAEs etc.), and provides such information to safety department and other relevant departments, within the required time frames. * Completes monitoring visit reports within the agreed timelines * Ensure local and global clinical study tracking databases are kept current with clinical study information as required (i.e. e-track, Veeva, RAMOS). * Ensure all necessary study supplies are available at sites in a timely manner and appropriate accountability is maintained during the study. Ensure all unused study supplies are accounted for and destroyed appropriately. * Ensure sponsor study records are inspection ready at all times and archives records as applicable Qualifications You are: Education required: * Undergraduate degree or its international equivalent in clinical, science, or health-related fieldfrom an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience preferred Skills Required * Read, write and speak fluent English; fluent in host country language required. * 4+ years of clinical monitoring experience required * Knowledge of ICH and local regulatory authority regulations regarding drug * Clinical research experience * Knowledge of ICH and local regulatory authority regulations regarding drug * Experience in monitoring all trial components (PSSV to COV) * Experience in coaching/mentoring other CRA What ICON can offer you:Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.Our benefits examples include: * Various annual leave entitlements * A range of health insurance offerings to suit you and your family's needs * Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead * Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family's well-being * Life assurance * Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others Pay Range ($110,520.00 - $138,150.00 USD) Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level. Visit our careers website to read more about the benefits of working at ICON: ************************************ At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we've done to become a more inclusive organisation. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. ***************************************************** Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.

Cutera, Inc. is a leading aesthetics device company with a comprehensive product portfolio and a worldwide distribution footprint. The Company's technology enables physicians to provide sophisticated solutions for a wide range of medical aesthetic applications. We are looking for a key member to join our fast-paced R&D engineering team in changing the landscape of medical aesthetics. Please visit ************** for more information about us! Job Description Position Summary: We are seeking a Senior Clinical Research Associate to join our clinical team in its mission to improve lives through medical aesthetic technologies driven by science. Our products use a broad range of innovative laser and radio frequency technologies designed by our scientists and engineers to enable first-to-market applications and best-in-class products for dermatology. Reporting to the Director of Clinical Research, the Senior CRA is responsible for leading and coordinating activities among participating study physicians and maintaining study records. Serving as the primary point of contact for study sites, this role oversees the organization and execution of pre- and post-market clinical research studies. The Senior CRA collaborates with research staff to uphold best practices, ensuring study integrity and accurate data documentation. Additionally, you will establish and maintain relationships with investigators, site coordinators, and regulatory personnel, ensuring compliance with GCP guidelines and all relevant clinical study regulations. Duties & Responsibilities: * Lead the development, production and compilation of study documents such as protocol, case report forms (paper or electronic), informed consent, subject questionnaire, clinical study reports, clinical portions of applicable regulatory submissions, IRB submission, data management or statistical analysis plans or other controlled documentation. * Perform site qualification, study initiation, site training, interim monitoring and study close-out visits, and complete timely and accurate site visit reports. * Design forms (electronic or paper based) for receiving, processing, or tracking data. * Develop and maintain study and data tracking tools and report study/ data metrics to supervisory staff. * Track and ensure the timely flow of study documentation and case report forms, including in-house data flow and/or electronic forms transfer. * Monitor data -- remotely, on site, and via other approved modes - with a focus on data integrity (completeness, accuracy, consistency, timeliness) and patient safety. * Create and manage clinical databases and process clinical data, including receipt, entry, verification, or filing of information. * Prepare data analysis listings and activity, performance, or progress reports. * Generate data queries and liaise with the study sites to resolve identified problems in a timely manner. * Prepare and maintain the study essential documents including sponsor and site-specific regulatory documentation (binders or eTMF) * Write work instruction manuals, data capture guidelines, and other study specific standard operating procedures. * Consistently assess processes, systems, and technologies for efficiency and compliance with procedures; suggest revision to increase productivity as applicable. * Analyze clinical data using appropriate statistical tools * Help record and track clinical trial data on online government databases. (*********************** * Help select specific software programs for various research procedures and scenarios as needed. * Train staff on study procedures, photography and software program usage. * Provide support and information to functional areas such as clinical affairs, regulatory, research & development and marketing. * Ensure study documentation, procedures, data collection and analysis are conducted in accordance with Cutera SOPs, FDA regulations, ICH Good Clinical Practice (GCP) guidelines and other applicable regulations. * Other duties as assigned. Qualifications Minimum Requirements & Qualifications: * B.Sc. in the life sciences or allied health/medical related field, or equivalent experience. * 3+ years of experience in a clinical research environment preferred. * Experience independently running a study from start-up through close-out required. * Experience in the medical device and/or dermatology or aesthetic space preferred. * Knowledge of GCP guidelines, medical terminology and clinical trial processes required. * Proficient in the use of Microsoft Office Applications (Word, Excel, PowerPoint, etc.) * Working knowledge of EDC, eTMF and/or other clinical research or data management software preferred. * Experience participating in FDA bioresearch monitoring (BIMO) audits preferred. * Strong interpersonal and organizational skills. * Excellent oral and written communication skills. * Strong organizational skills with attention to details. * Self-motivated, flexible, and independent thinker. * Ability to work in a fast-paced/demanding environment. * Problem solver, ability to prioritize and/or multi-task * Collaborative team member * Must be willing to work on-site at corporate headquarters in Brisbane, CA (Monday through Friday). * Travel up to 30 percent of the time. Additional Information Compensation: Cutera expects to reasonably pay in the range listed below for this position based on the city and state listed in the job posting. The actual compensation is influenced by a wide array of factors, including but not limited to skill set, level of experience, education, and candidate residence if the position is remote or field-based. Base salary range: $110,000 - $130,000 All your information will be kept confidential according to EEO guidelines. If you are ready to become part of our spectacular, growing, and FUN company, then apply today! We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, perform essential job functions, and receive other benefits and privileges of employment. Please contact us to request accommodation. Applicants responding to this posting must be able to provide proof of eligibility to work in the United States. Competitive salary, benefits, ESPP and stock options. Cutera is an Equal Employment Opportunity Employer.

Science 37's Nursing Solutions Group brings together expert nurses who share a passion for organizing, planning and implementing mobile clinical nurse services to participants in clinical trials. Science 37's extraordinary work environment allows continuous collaboration between clinicians, clinical researchers, patient recruitment specialists, data managers and technology developers. The Nursing Solutions Group is involved throughout the trial life cycle, from protocol development and feasibility analysis to clinical trial implementation and closeout. The Per Diem Mobile Research Nurse is a Registered Nurse who will work per diem and has experience across multiple therapeutic areas with the ability to work independently and integrate well with the Nursing Solutions Group. With interest/expertise in Science 37's decentralized model of care delivery, the Mobile Research Nurse will perform delivery of care to participants as well as collaborate with brick and mortar sites, if indicated, for shared clinical trial implementation. The Mobile Research Nurse ensures the professional delivery of patient care in compliance with all federal and state regulations, Good Clinical Practice, and Standard Operating Procedures. *This is a travel role that requires on-site visits to participants homes. Duties for this position include but are not limited to: Participate and provide research nurse services to qualified study participants at home Apply clinical research and nursing practices to develop solutions to complex problems Collaborate with Lead and Per Diem Mobile Research Nurses on solutioning, education, and resource support Participate in activities that will further the operational development of Science 37 nursing service delivery Develop relationships with study team members and serve as the subject matter expert (SME) on all nursing processes Other duties as assigned as the needs of Science 37 evolve and change This position has the following qualifications: BSN degree preferred Full Covid Vaccination strongly preferred. Science 37 follows CDC guidelines for vaccination recommendations and such guidelines are subject to change. Active RN licensure in home state as well as eligibility for Compact Licensure required Minimum 2+ years clinical/research experience preferred Basic Life Support (BLS) Certification Maintain a positive reflection of the company by representation in participant's homes or in clinic settings Travel and availability qualifications are as follows: 1-2 days minimum a week dedicated to support Science 37's study visits Weekday/night availability required Must be willing to travel to a participants homes Active Driver's License Science 37 is looking for people with the following skills and competencies: BSN degree preferred Active RN licensure in home state as well as eligibility for Compact Licensure required Minimum 2+ years clinical/research experience preferred Basic Life Support (BLS) Certification Active Driver's License Weekday/night availability required Maintain a positive reflection of the company by representation in participant's homes or in clinic settings Up to 100% travel, as needed, for study participant visits, project team meetings, and other professional meetings/conferences as needed Ability to obtain nursing license in multiple states based on study needs Physical ability to perform nursing tasks and lift equipment up to 15 kg in weight Access to a reliable vehicle to perform study participant visits and transport equipment Ability to drive to local and/or remote locations to perform study participant visits Ability to use technology effectively and appropriately for study participant assessments and documentation including but not limited to study participant care equipment, laptop computers, communication devices and tablets Ability to communicate in English (both verbal and written) There is minimal supervision for this position, with individuals reporting to the Manager, Nursing Solutions Group. Compensation varies based on location and work being performed. The starting pay range for a candidate selected for this position is generally within the range of $50-55 per hour. Employees may be eligible for additional discretionary bonuses and commissions. The successful candidate's actual pay will also be based on qualifications and experience, so the actual starting pay may be above or below this range. Science 37 is an equal opportunity employer. We are committed to creating a diverse environment and is an equal opportunity employer. All qualified applicants receive consideration for employment without regard to age, race, ethnicity (including but not limited to hair texture and protected hairstyles), ancestry, color, sex, national origin, sexual orientation, gender, gender identity, gender expression, transgender status, religious creed, physical or mental disability (including actual or perceived disability), medical condition (including HIV/AIDS), pregnancy, perceived pregnancy and pregnancy related conditions, genetic information, marital status, political affiliation or activities, status as a victim of domestic violence, assault, or stalking, veteran status or participation in the uniformed military services of the United States, including the National Guard, or any other basis prohibited by applicable law. Science 37 values the well-being of its employees and aims to provide team members with everything they need to succeed. Submit your resume to apply! To learn about Science 37's privacy practices including compliance with applicable privacy laws, please click here

Transform Lives with Us: ABA Program Supervisor ABA Clinical Coordinator (Program Supervisor) Why You'll Love Working Here: • Comprehensive Benefits: Health, dental, vision insurance, 401k, and more. • Professional Development: Supervision for BCBA certification and career advancement opportunities. • Flexible Work-Life Balance: Enjoy 80 hours of PTO annually and flexible scheduling. • State-of-the-Art Resources: Equipped with the latest technology, plus a cell phone and laptop. • Meaningful Impact: Create and implement personalized ABA programs, collaborate with families, and mentor staff. Your Role: • Lead and supervise ABA programs to ensure client progress. • Provide clinical training and support to a dedicated team. • Foster a collaborative environment for family and team engagement. What You Bring: • Master's Degree in Applied Behavior Analysis, Psychology, or related field. • 1-2+ years of clinical supervision experience. • Bilingual in Spanish preferred. • Excellent communication and analytical skills. • Valid California Driver's License and clean driving record & Immunization records: Rubella (2-series child/1-series adult) Rubeola (2-series child/1-series adult) Mumps (2-series child/1-series adult) Varicella (2-series) Hepatitis B (3-series) (Declination acceptable) Pertussis (Tdap) (Declination acceptable) Absence of Tuberculosis (TB) Negative TB test must be conducted within three months prior to start date with CCS clients, and TB test must be conducted if practitioner is exposed to TB, according to CDC guidance for Health Care Professionals Join a team that's committed to making a difference. Apply now at ********************************* and start your journey with us! Additional Information BTA is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender, gender identity, sexual orientation, marital status, national origin, disability, age or covered veteran status

Job DescriptionPrimary Duties and Responsibilities The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Evaluates and abstracts research data and ensures compliance with protocol and research objectives. Responsible for completing case report forms, entering clinical research data, and assist with regulatory submissions to the IRB. Provides limited patient contact as needed for study and assist with study budget and patient research billing. Ensures compliance with all federal, local, FDA, IRB, and HIPAA guidelines and regulations pertaining to the study and patient care. Primary Duties and Responsibilities Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement study. Evaluates and abstracts clinical research data from source documents. Ensures compliance with protocol and overall clinical research objectives. Completes Case Report Forms (CRFs). Enters clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors. Provides supervised patient contact or patient contact for long term follow-up patients only. Assists with regulatory submissions to the Institutional Review Board (IRB) including submission of Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines. Assists with clinical trial budgets. Assists with patient research billing. Schedules patients for research visits and research procedures. Responsible for sample preparation and shipping and maintenance of study supplies and kits. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board. Maintains research practices using Good Clinical Practice (GCP) guidelines. Maintains strict patient confidentiality according to HIPAA regulations and applicable law. Participates in required training and education programs. QualificationsRequirements: High School Diploma/GED required. Bachelor's Degree preferred. #Jobs-Indeed Req ID : 4666 Working Title : Clinical Research Associate I, PER DIEM - Tan Lab Department : Cancer - Research Center Health Equity Business Entity : Cedars-Sinai Medical Center Job Category : Academic / Research Job Specialty : Research Studies/ Clin Trial Overtime Status : NONEXEMPT Primary Shift : Day Shift Duration : 8 hour Base Pay : $19.50 - $32.86

Title: Clinical Trial Coordinator Contract to Hire: 6-month contract Responsibilities: Assist in operational and administrative research support under the clinical direction of the Principal Investigator (PI) Ensure compliance with institutional, federal, and sponsor regulations (e.g., FDA, IRB) Maintain accurate and up-to-date regulatory documents and study records Obtain informed consent from study participants under investigator supervision. Schedule and coordinate participant visits and follow-ups. Requirements: High School Diploma ~1 year of experience working in clinical trials Strong Organizational and Communication skills Ability to work effectively on cross-functional teams Prior experience in a Clinical Trials setting is highly preferred

In this role you will ensure IRB approved protocols are implemented and followed; execute the informed consent process and monitor patient status and safety; collect and organize research data; schedule and conduct study-specific training and site in-services to study related staff on new or amended protocols, and educate patients and their families about treatments and possible side effects. The Clinical Research Coordinator must also be able to perform clinical tasks. Responsibilities: ● Site preparation. ● Obtaining informed consent, patient screening and recruitment. ● Patient enrollment, and conducting study visits. ● Maintaining and dispensing study product and supplies. ● Completing and ensuring the quality of case report forms. ● Maintaining source documents ● Ensuring site quality. ● Maintain a thorough and meticulous working knowledge of protocol schemas and requirements. ● Collaborate with physicians to maintain strict protocol adherence and serve as a resource for members of staff. ● Writes patient information sheet for clinical studies for submission to IRB, as well as complete the necessary documents for IRB admission in a timely fashion. ● Participate in the development and implementation of patient educational materials. ● Writes patient information sheet (ICF) for clinical studies for admission to IRB, as well as complete the necessary documents for IRB submission in a timely fashion. ● Review research and administrative documents to determine action items, prioritizing and tracking action items. ● Responsible for completion, submission and tracking of regulatory documents to the IRB. Details: Location: Modesto, CA Pay: $60k-$70k (Dependent on background and years of experience) Hours: Monday - Friday; Normal Business Hours; Onsite 5 Days a Week Duration: Direct Hire

Science 37's Nursing Solutions Group brings together expert nurses who share a passion for organizing, planning and implementing mobile clinical nurse services to participants in clinical trials. Science 37's extraordinary work environment allows continuous collaboration between clinicians, clinical researchers, patient recruitment specialists, data managers and technology developers. The Nursing Solutions Group is involved throughout the trial life cycle, from protocol development and feasibility analysis to clinical trial implementation and closeout. The Per Diem Mobile Research Nurse is a Registered Nurse who will work per diem and has experience across multiple therapeutic areas with the ability to work independently and integrate well with the Nursing Solutions Group. With interest/expertise in Science 37's decentralized model of care delivery, the Mobile Research Nurse will perform delivery of care to participants as well as collaborate with brick and mortar sites, if indicated, for shared clinical trial implementation. The Mobile Research Nurse ensures the professional delivery of patient care in compliance with all federal and state regulations, Good Clinical Practice, and Standard Operating Procedures. * This is a travel role that requires on-site visits to participants homes. Duties for this position include but are not limited to: * Participate and provide research nurse services to qualified study participants at home * Apply clinical research and nursing practices to develop solutions to complex problems * Collaborate with Lead and Per Diem Mobile Research Nurses on solutioning, education, and resource support * Participate in activities that will further the operational development of Science 37 nursing service delivery * Develop relationships with study team members and serve as the subject matter expert (SME) on all nursing processes * Other duties as assigned as the needs of Science 37 evolve and change This position has the following qualifications: * BSN degree preferred * Full Covid Vaccination strongly preferred. Science 37 follows CDC guidelines for vaccination recommendations and such guidelines are subject to change. * Active RN licensure in home state as well as eligibility for Compact Licensure required * Minimum 2+ years clinical/research experience preferred * Basic Life Support (BLS) Certification * Maintain a positive reflection of the company by representation in participant's homes or in clinic settings * Travel and availability qualifications are as follows: * 1-2 days minimum a week dedicated to support Science 37's study visits * Weekday/night availability required * Must be willing to travel to a participants homes * Active Driver's License Science 37 is looking for people with the following skills and competencies: * BSN degree preferred * Active RN licensure in home state as well as eligibility for Compact Licensure required * Minimum 2+ years clinical/research experience preferred * Basic Life Support (BLS) Certification * Active Driver's License * Weekday/night availability required * Maintain a positive reflection of the company by representation in participant's homes or in clinic settings * Up to 100% travel, as needed, for study participant visits, project team meetings, and other professional meetings/conferences as needed * Ability to obtain nursing license in multiple states based on study needs * Physical ability to perform nursing tasks and lift equipment up to 15 kg in weight * Access to a reliable vehicle to perform study participant visits and transport equipment * Ability to drive to local and/or remote locations to perform study participant visits * Ability to use technology effectively and appropriately for study participant assessments and documentation including but not limited to study participant care equipment, laptop computers, communication devices and tablets * Ability to communicate in English (both verbal and written) There is minimal supervision for this position, with individuals reporting to the Manager, Nursing Solutions Group. Compensation varies based on location and work being performed. The starting pay range for a candidate selected for this position is generally within the range of $50-55 per hour. Employees may be eligible for additional discretionary bonuses and commissions. The successful candidate's actual pay will also be based on qualifications and experience, so the actual starting pay may be above or below this range. Science 37 is an equal opportunity employer. We are committed to creating a diverse environment and is an equal opportunity employer. All qualified applicants receive consideration for employment without regard to age, race, ethnicity (including but not limited to hair texture and protected hairstyles), ancestry, color, sex, national origin, sexual orientation, gender, gender identity, gender expression, transgender status, religious creed, physical or mental disability (including actual or perceived disability), medical condition (including HIV/AIDS), pregnancy, perceived pregnancy and pregnancy related conditions, genetic information, marital status, political affiliation or activities, status as a victim of domestic violence, assault, or stalking, veteran status or participation in the uniformed military services of the United States, including the National Guard, or any other basis prohibited by applicable law. Science 37 values the well-being of its employees and aims to provide team members with everything they need to succeed. Submit your resume to apply!

This role follows a hybrid work schedule; however, we can only consider applicants who will be able to commute to our Los Angeles work location a few times per week. If hired you must reside in the commutable area. The Clinical Research Coordinator II works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information. Presents information at regular research staff meetings. May plan and coordinate strategies for increasing patient enrollment, improving efficiency, training of personnel, or identifying new research opportunities. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Primary Duties and Responsibilities Independent study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and participating in the informed consent process. Schedules patients for research visits and procedures. In collaboration with the physician and other medical personnel, documents thoroughly on Case Report Forms (CRFs) the following; changes in patient condition, adverse events, concomitant medication use, protocol compliance, response to study drug. Maintains accurate source documents related to all research procedures. Responsible for accurate and timely data collection, documentation, entry, and reporting including timely response to sponsor queries. Schedules and participates in monitoring and auditing activities. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information; present this information at regular research staff meetings. Notifies direct supervisor about concerns regarding data quality and study conduct. Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events, protocol deviations, and Safety Letters in accordance with local and federal guidelines. May perform other regulatory / Institutional Review Board duties, budgeting duties, and assisting with patient research billing and reconciliation. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA and local Institutional Review Board. Maintains research practices using Good Clinical Practice (GCP) guidelines. Maintains strict patient confidentiality according to HIPAA regulations and applicable law. May coordinate training and education of other personnel. May participate in centralized activities such as auditing, Standard Operating Procedure development, etc. May plan and coordinate strategies for increasing patient enrollment, and/or improving clinical research efficiency. May identify quality and performance improvement opportunities and collaborate with staff in the development of action plans to improve quality. May identify new research opportunities and present to investigators Participates in required training and education programs. Qualifications This role follows a hybrid work schedule; however, we can only consider applicants who will be able to commute to our Los Angeles work location a few times per week. If hired you must reside in the commutable area. Requirements: High School Diploma/GED required. Bachelor's Degree Science, Sociology or related degree preferred. 2 years Clinical research related experience required. #Jobs-Indeed Req ID : 5685 Working Title : Clinical Research Coordinator II (Hybrid) Department : Cancer - SOCCI Clinical Research Business Entity : Cedars-Sinai Medical Center Job Category : Academic / Research Job Specialty : Research Studies/ Clin Trial Overtime Status : EXEMPT Primary Shift : Day Shift Duration : 8 hour Base Pay : $28.30 - $48.11

Title: Clinical Trial Coordinator Contract to Hire: 6-month contract Responsibilities: Assist in operational and administrative research support under the clinical direction of the Principal Investigator (PI) Ensure compliance with institutional, federal, and sponsor regulations (e.g., FDA, IRB) Maintain accurate and up-to-date regulatory documents and study records Obtain informed consent from study participants under investigator supervision. Schedule and coordinate participant visits and follow-ups. Requirements: High School Diploma ~1 year of experience working in clinical trials Strong Organizational and Communication skills Ability to work effectively on cross-functional teams Prior experience in a Clinical Trials setting is highly preferred

Science 37's Nursing Solutions Group brings together expert nurses who share a passion for organizing, planning and implementing mobile clinical nurse services to participants in clinical trials. Science 37's extraordinary work environment allows continuous collaboration between clinicians, clinical researchers, patient recruitment specialists, data managers and technology developers. The Nursing Solutions Group is involved throughout the trial life cycle, from protocol development and feasibility analysis to clinical trial implementation and closeout. The Per Diem Mobile Research Nurse is a Registered Nurse who will work per diem and has experience across multiple therapeutic areas with the ability to work independently and integrate well with the Nursing Solutions Group. With interest/expertise in Science 37's decentralized model of care delivery, the Mobile Research Nurse will perform delivery of care to participants as well as collaborate with brick and mortar sites, if indicated, for shared clinical trial implementation. The Mobile Research Nurse ensures the professional delivery of patient care in compliance with all federal and state regulations, Good Clinical Practice, and Standard Operating Procedures. *This is a travel role that requires on-site visits to participants homes. Duties for this position include but are not limited to: Participate and provide research nurse services to qualified study participants at home Apply clinical research and nursing practices to develop solutions to complex problems Collaborate with Lead and Per Diem Mobile Research Nurses on solutioning, education, and resource support Participate in activities that will further the operational development of Science 37 nursing service delivery Develop relationships with study team members and serve as the subject matter expert (SME) on all nursing processes Other duties as assigned as the needs of Science 37 evolve and change This position has the following qualifications: BSN degree preferred Full Covid Vaccination strongly preferred. Science 37 follows CDC guidelines for vaccination recommendations and such guidelines are subject to change. Active RN licensure in home state as well as eligibility for Compact Licensure required Minimum 2+ years clinical/research experience preferred Basic Life Support (BLS) Certification Maintain a positive reflection of the company by representation in participant's homes or in clinic settings Travel and availability qualifications are as follows: 1-2 days minimum a week dedicated to support Science 37's study visits Weekday/night availability required Must be willing to travel to a participants homes Active Driver's License Science 37 is looking for people with the following skills and competencies: BSN degree preferred Active RN licensure in home state as well as eligibility for Compact Licensure required Minimum 2+ years clinical/research experience preferred Basic Life Support (BLS) Certification Active Driver's License Weekday/night availability required Maintain a positive reflection of the company by representation in participant's homes or in clinic settings Up to 100% travel, as needed, for study participant visits, project team meetings, and other professional meetings/conferences as needed Ability to obtain nursing license in multiple states based on study needs Physical ability to perform nursing tasks and lift equipment up to 15 kg in weight Access to a reliable vehicle to perform study participant visits and transport equipment Ability to drive to local and/or remote locations to perform study participant visits Ability to use technology effectively and appropriately for study participant assessments and documentation including but not limited to study participant care equipment, laptop computers, communication devices and tablets Ability to communicate in English (both verbal and written) There is minimal supervision for this position, with individuals reporting to the Manager, Nursing Solutions Group. Compensation varies based on location and work being performed. The starting pay range for a candidate selected for this position is generally within the range of $50-55 per hour. Employees may be eligible for additional discretionary bonuses and commissions. The successful candidate's actual pay will also be based on qualifications and experience, so the actual starting pay may be above or below this range. Science 37 is an equal opportunity employer. We are committed to creating a diverse environment and is an equal opportunity employer. All qualified applicants receive consideration for employment without regard to age, race, ethnicity (including but not limited to hair texture and protected hairstyles), ancestry, color, sex, national origin, sexual orientation, gender, gender identity, gender expression, transgender status, religious creed, physical or mental disability (including actual or perceived disability), medical condition (including HIV/AIDS), pregnancy, perceived pregnancy and pregnancy related conditions, genetic information, marital status, political affiliation or activities, status as a victim of domestic violence, assault, or stalking, veteran status or participation in the uniformed military services of the United States, including the National Guard, or any other basis prohibited by applicable law. Science 37 values the well-being of its employees and aims to provide team members with everything they need to succeed. Submit your resume to apply! To learn about Science 37's privacy practices including compliance with applicable privacy laws, please click here