NewAssociate Director, Product Safety & Compliance Caraway HomeAssociate Director, Product Safety & ComplianceNew York, NYRemoteFull timeDeep, working knowledge of food contact material regulations including FDA 21 CFR, LFGB (Chapters 30/31), EU Framework Regulation (EC) No 1935/2004, REACH, CA Prop 65, CA AB 1200, FSC, NSF, and the Colorado PFAS Chemicals Consumer Protection Act; familiarity with UK REACH and other international frameworks is a strong plus. Design and manage Caraway's testing strategy, selecting and managing third-party labs (particularly in Asia, including NRTLs for small appliances), defining testing scope and frequency by product type and risk level, and sequencing testing within development timelines to avoid launch delays or costly late-stage findings.
NewScientific Associate (Associate Expert Potency) eTeam Inc.Scientific Associate (Associate Expert Potency)East Hanover, NJ$35–$43 / hourThe Associate Expert, Science & Technology (Research associate) performs routine testing and to develop bioassays suitable for lot disposition and characterization of gene therapy drug substances and drug products. Participate in cross-functional activities including critical reagent management, in-process sample handling, process development analytical supports, and assay method transfers to Quality Control/Clinical Research Organization laboratories.
Licensed Clinical Psychologist (On-site, NY) Talent Pool, Upcoming Opportunities Brightline IncLicensed Clinical Psychologist (On-site, NY) Talent Pool, Upcoming OpportunitiesNew York, NY$125,000–$150,000 / yearIn addition to Brightline's generalized support, we offer focused programs to support anxiety, Obsessive Compulsive Disorders (OCD), Attention-Deficit/Hyperactivity Disorder (ADHD), and disruptive behaviors. Brightline is based in Palo Alto and is backed by investors including Boston Children's Hospital, Northwell Health, Blue Cross Blue Shield of Massachusetts, Google Ventures, KKR, and Oak HC/FT.
Senior Global Clinical Study Manager IQVIA Holdings IncSenior Global Clinical Study ManagerNew York, NY$93,100–$232,800 / yearWe are seeking a Global Study Manager responsible for the end-to-end planning, execution, and delivery of clinical trial site management activities across global studies. Drive global clinical trials from first site activation to final patient visit-own the strategy, accelerate delivery, and shape the future of clinical research worldwide.
Patient Cloud Training Specialist (Remote) Medidata Solutions IncPatient Cloud Training Specialist (Remote)Iselin, NJRemote$79,500–$106,000 / yearAbout the Team: As a member of the Medidata Global Education team, your mission is to support the successful implementations of client study protocols and related Instructor-Led Training -producing quality training materials and exceptional training experiences for clinical trial operations personas responsible for study fulfillment and associated patient interactions. Celebrating over 25 years of ground-breaking technological innovation across more than 38,000 trials and 12 million patients, Medidata offers industry-leading expertise, analytics-powered insights, and one of the largest clinical trial data sets in the industry.
Medical Science Liason (MSL) - Podiatry, Men’s Health and Ortho (Northeast) Mallinckrodt PharmaceuticalsMedical Science Liason (MSL) - Podiatry, Men’s Health and Ortho (Northeast)Newark, New JerseyRemoteThis is a field-based Medical Affairs position requiring a strong scientific background (technical or clinical experience) as the MSL will be a credible source of clinical/scientific data as well as technical/practical education to practicing clinicians, key opinion leaders (KOL), professional societies, and payers. A Medical Science Liaison (MSL) will serve as a liaison to the medical/scientific community and will be responsible for establishing, developing and maintaining relationships with key stakeholders within the geographic and therapeutic area of coverage.
Assistant Professor, Associate Professor, Professor Pediatric Cardiology Rutgers The State University of New JerseyAssistant Professor, Associate Professor, Professor Pediatric CardiologyNew Brunswick, NJThe Department of Pediatrics at Rutgers Robert Wood Johnson Medical School (RWJMS), in partnership with Bristol-Myers Squibb Children's Hospital (BMSCH) at Robert Wood Johnson University Hospital, is seeking a pediatric cardiologist to join a growing, comprehensive pediatric cardiovascular program serving children and families throughout New Jersey. The New Brunswick academic campus brings together Bristol-Myers Squibb Children's Hospital, Robert Wood Johnson University Hospital, the Child Health Institute of New Jersey, and nearby Children's Specialized Hospital, creating a collaborative environment for the care of medically and surgically complex children.
Associate Professor of Transplant Surgery Rutgers The State University of New JerseyAssociate Professor of Transplant SurgeryNew Brunswick, NJAs an attending at Rutgers, Robert Wood Johnson Medical School and Robert Wood Johnson University Hospital in New Brunswick, responsibilities will include all aspects of patient care and medical record completion, teaching of students, residents, and fellows via clinical patient rounds, Grand Rounds, and departmental conferences; participation in community education programs and lecture series; submission of abstracts/manuscripts for publication; and other duties as assigned by the Division Chief, Chair, or Dean. Under Policy 100.3.1 Immunization Policy for Covered Individuals, if employment will commence during Flu Season, Rutgers University may require certain prospective employees to provide proof that they are vaccinated against Seasonal Influenza for the current Flu Season, unless the University has granted the individual a medical or religious exemption.
Executive Director, Clinical Development, Breast Cancer BeOne Medicines AGExecutive Director, Clinical Development, Breast CancerNY$329,700–$409,700 / yearSpecifically, the incumbent will collaborate with a variety of internal and external partners and stakeholders, such as clinical investigators, scientists and key opinion leaders (KOLs), as well as multidisciplinary internal groups, including other groups in Clinical Development, research, business development, commercial operations, legal, translational science etc. The Executive Director, Clinical Development will effectively lead BeOne clinical assets through successful development of early and late phase clinical development strategies and deliverables in partnership with multiple functions across the organization, and with external academicians and collaboration partners.
Senior Director Clinical Development, Solid Tumor BeOne Medicines AGSenior Director Clinical Development, Solid TumorNY$299,800–$369,800 / yearProvide guidance/training to function team in Execution Unit, CRO staff and study site staff on the therapeutical area, molecule, and/or clinical protocol and may provide coach and mentorship to the team members working on the assets when there's performance concern and for team development purpose. Through SuperHighway partnerships, highly promising assets from leading biotech partners can access our development capabilities creating a true win-win ecosystem with the ultimate goal of helping more patients around the world.
Licensed Clinical Psychologist (New York/ On Site) Talent Pool, Upcoming Opportunities BrightlineLicensed Clinical Psychologist (New York/ On Site) Talent Pool, Upcoming OpportunitiesNew York, New York$125,000–$150,000 / yearIn addition to Brightline’s generalized support, we offer focused programs to support anxiety, Obsessive Compulsive Disorders (OCD), Attention-Deficit/Hyperactivity Disorder (ADHD), and disruptive behaviors. Brightline is based in Palo Alto and is backed by investors including Boston Children’s Hospital, Northwell Health, Blue Cross Blue Shield of Massachusetts, Google Ventures, KKR, and Oak HC/FT.
Associate Director - Medical Science Liaison - Dermatology - CT & NY EAST Lilly USAAssociate Director - Medical Science Liaison - Dermatology - CT & NY EASTWhite Plains, ConnecticutOur current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women’s Initiative for Leading at Lilly (WILL). The Medical Science Liaison (MSL) program is specifically designed to meet these needs through a field-based group of medical professionals with deep content knowledge about specific disease states, Lilly and competitive compounds and landscape in the therapeutic areas they represent.
Clinical Supply Chain Project Leader SanofiClinical Supply Chain Project LeaderMorristown, NJ$105–$151.67 / hourThe CSC-PL will also ensure clear, concise, consistent, and timely communication with stakeholders and act as a change agent through the leadership of global initiatives targeting process improvement and engaging all partners throughout the clinical supply chain. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen.
Senior Scientist, Regulatory & Clinical Operations hims & hersSenior Scientist, Regulatory & Clinical OperationsSouth Plainfield, NJYou Have: PhD in Clinical Chemistry, Biochemistry, Analytical Chemistry, Molecular Biology, or related field with 4+ years; OR Master's degree with 7+ years; OR Bachelor's degree with 10+ years of relevant bench experience in a diagnostic or clinical laboratory setting. The ideal candidate is comfortable operating at the intersection of bench science and clinical study execution, translates regulatory rigor into practical day-to-day decisions, and thrives working independently in a fast-moving environment.
Senior Manager, Global Clinical Regulatory Lead PTC TherapeuticsSenior Manager, Global Clinical Regulatory LeadWarren, NJ$130,000–$164,600 / yearJob Description Summary: The Senior Manager, Global Clinical Regulatory Lead, is responsible for providing strategic and operational direction for the planning, management, support and execution of regulatory activities for PTC drug products (clinical and commercial) within the US as applicable. Clinical Trial Applications (CTAs): Initiate and execute CTA/CTNs in US, EU, and globally by keeping up to date with regulations and critically analyzing the interactions with health authorities to ensure that any outstanding issues are addressed.
Clinical Database, SME - Strategy (CDI Specialist) Akasa IncClinical Database, SME - Strategy (CDI Specialist)NY$130,000–$165,000 / yearSome of our recent recognitions include being named one of Americas Top Startup Employers 2026 by Forbes, #1 most promising healthcare RCM startup of 2025 by Black Book Market Research, and one of the fastest-growing GenAI startups to watch by AIM Research. Cross-functional in nature, this role not only interfaces regularly with R&D, it also sits in front of customers to help translate local clinical practices back to the team so the product fits the way the customer's clinicians actually work.
Senior Project Manager, Clinical Biomarker BeOne Medicines AGSenior Project Manager, Clinical BiomarkerNY$140,100–$185,100 / yearCollaborate and communicate with internal functional stakeholders including biomarker scientists, clinical operations and others, to drive the biomarker related works for clinical trials, such as manage lab vendors timeline, control biomarker budget, ensure compliance and quality, etc. Essential Functions of the job: Independently manage biomarker and bio-sample testing activities for clinical trials, including but not limited to review and finalize lab vendors key documents (such as lab manual, lab database design documents, contracts & budget, etc.
2027 Future Talent Program - Global Clinical Supply - Intern Merck & Co Inc2027 Future Talent Program - Global Clinical Supply - InternRahway, NJ$39,908–$111,111 / yearThis role offers a unique opportunity to work alongside leaders and subject matter experts while developing analytical, project management, and business acumen skills within the pharmaceutical industry. Interns will lead meaningful projects that contribute to business objectives, operational excellence, digital transformation, and continuous improvement efforts across a global organization.
2027 Future Talent Program - Global Clinical Supply - Co-op Merck & Co Inc2027 Future Talent Program - Global Clinical Supply - Co-opRahway, NJ$39,908–$111,111 / yearCompared with a summer internship, the co-op assignment provides additional time to understand business context, build stakeholder relationships, execute against project milestones, refine deliverables, and support implementation or handoff of solutions that create lasting value for GCS. Co-Ops will own meaningful workstreams that contribute to business objectives, operational excellence, digital transformation, data-driven decision making, and continuous improvement across a global organization.
Clinical Systems IT Manager Clinilabs IncClinical Systems IT ManagerNYRemote$120,000–$130,000 / yearOperationally oversee Clinilabs AWS service provider to ensure Corelab clinical systems do not run into capacity issues, backups are run, patches are applied and systems always remain recoverable in alignment with Clinilabs DR policy. Excellent interpersonal and communication skills, with the ability to collaborate effectively with business leaders, application developers, DBAs and vendors to gather and translate business requirements.