Clinical Data Specialist Iterative Scopes IncClinical Data SpecialistBoston, MAThis position is responsible for conducting detailed EHR reviews to identify potential clinical trial candidates, supporting patient recruitment efforts, maintaining research databases, and ensuring accurate documentation throughout the patient pre-screening process. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors'' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need.
Senior Clinical Consultant, Health and Risk Solutions Sun Life Financial IncSenior Clinical Consultant, Health and Risk SolutionsWellesley Hills, MA$78,600–$117,900 / yearThrough employers, industry partners and government programs, Sun Life U.S. offers a portfolio of benefits and services, including dental, vision, disability, absence management, life, supplemental health, medical stop-loss insurance, and healthcare navigation. At Sun Life, we prioritize your well-being with comprehensive benefits, including generous vacation and sick time, market-leading paid family, parental and adoption leave, medical coverage, company paid life and AD&D insurance, disability programs and a partially paid sabbatical program.
Sr. Research Associate, Clinical Biomarker Laboratory, Flow Cytometry Moderna IncSr. Research Associate, Clinical Biomarker Laboratory, Flow CytometryNorwood, MA$74,000–$118,400 / yearWe are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S. If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities. The Role: Moderna is seeking a talented and motivated Senior Research Associate to join the Clinical Flow Cytometry group to serve as a technical expert for the generation of high parameter flow cytometry data under GCLP guidelines to support clinical programs across multiple therapeutic areas.
Clinical Affairs Scientist Agilent Technologies IncClinical Affairs ScientistMA$105,280–$197,400 / yearThe candidate will work directly with pharmaceutical partners, R&D scientists, Clinical Trial Managers/ Clinical Research Associates, Quality Assurance, and Regulatory Affairs to assure compliance with internal and external requirements. We are searching for an experienced Clinical Affairs Scientist (CAS) to work within the medical diagnostic field as a key member of the Organization of Chief Medical Officer (OCMO) Global Clinical Affairs team.
Senior Manager Clinical Compliance Actalent IncSenior Manager Clinical ComplianceBrighton, MARemote$84–$89 / hourThis role oversees Trial Master File (TMF) inspection readiness, drives corrective and preventive action (CAPA) and continuous improvement activities, and partners closely with cross-functional teams and external vendors to maintain a robust GCP-compliant quality framework. The position offers the opportunity to spearhead clinical compliance for a growing biotechnology organization, support an exciting pipeline across multiple clinical trial phases, and work directly with executive leadership in a long-term, strategic capacity.
Clinical Project Manager - East Coast US - FSP ParexelClinical Project Manager - East Coast US - FSPBoston, MARemoteThe Project Manager drives the planning, execution, and delivery of internal initiatives across Study Management functions and reports directly to the Director, Clinical Operations. + Demonstrated end‑to‑end clinical trial management experience across Phase II and Phase III studies, with strong understanding of operational requirements from study start‑up through close‑out.
Head Of Asset In GU, Oncology Clinical Development AbbVie, IncHead Of Asset In GU, Oncology Clinical DevelopmentWaltham, MAPersonally or through a direct report, leads and demonstrates ownership of the design and implementation of multiple clinical development programs (or one large, complex program) in support of the overall product development plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations, and emerging issues. Acts as clinical lead and actively solicits opinion leader interactions related to the disease area(s); partners with Medical Affairs, Commercial and other functions in these activities as required, consistent with corporate policies, to ensure that broad cross-functional perspectives are incorporated into Clinical Development Plans and protocols as appropriate.
Senior Manager, Clinical Supply Chain Management Kiniksa Pharmaceuticals International PlcSenior Manager, Clinical Supply Chain ManagementLexington, MA$160,000–$170,000 / yearDirector, Clinical Supply Chain, the Senior Manager, Clinical Supply Chain Management will provide operational leadership and cross-functional coordination for end-to-end clinical supply activities across assigned clinical studies and programs. Demonstrated vendor management across packaging, labeling, depots, logistics providers, CMOs/CPOs, CROs, and IRT partners, including clear expectations, escalation pathways, and performance accountability.
Clinical Dietitian (Per Diem) With New Pay Rates! South Shore HealthClinical Dietitian (Per Diem) With New Pay Rates!Weymouth, MA$32.21–$46.06 / hourResponsibilities if Required: Education if Required: License/Registration/Certification Requirements: Dietitian/Nutritionist- Board of Registration of Dietitians and Nutritionists (Massachusetts), Dietitian Licensure Eligible- Massachusetts Department of Public Health (DPH) - Office of Health and Human Services (EOHHS), Registered Dietitian- Commission on Dietetic Registration, Registered Dietitian Eligible- Commission on Dietetic Registration. Documents which patients need assessment notes and the reasons; Documents daily multi-disciplinary care rounds on 'My Patients' Worklist and files in drawer daily.
Clinical Specialist Lucid Diagnostics IncClinical SpecialistBoston, MAThis includes but is not limited to: Hands-on training of other healthcare providers in the administration of EsoCheck to indicated patients; Leading peer-to-peer engagements and small-group educational events. CLINICAL SPECIALIST: The Clinical Specialist role primarily covers the Eastern region of the United States, and is 100% field based, requiring 65%+ travel.
Pioneering Medicines: Medical Director / Senior Medical Director, Clinical Development Lead Flagship Pioneering IncPioneering Medicines: Medical Director / Senior Medical Director, Clinical Development LeadCambridge, MA$215,000–$335,000 / yearFlagship has been recognized twice on FORTUNE's "Change the World" list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company's annual list of the World's Most Innovative Companies. Harnessing the drug development expertise of its team together with the power of Flagship''s multiple scientific platforms, Pioneering Medicines explores and identifies new product concepts which are then advanced jointly with Flagship's bioplatform companies.
Senior Director, Clinical Translational Scientist Kiniksa Pharmaceuticals CorpSenior Director, Clinical Translational ScientistLexington, MA$279,450–$302,220 / yearKiniksa is seeking an accomplished and strategic Senior Director, Clinical Translational Scientist reporting to GVP, Research & Non-Clinical Development to play a critical leadership role in advancing clinical-stage development programs from early clinical development through proof-of-concept and registrational studies. This individual will serve as a key scientific leader across multidisciplinary teams, integrating insights from Research, Clinical Development, Clinical Pharmacology, Bioanalysis, Biostatistics, Regulatory Affairs, and Medical Affairs to maximize the probability of technical and regulatory success across the portfolio.
NewAssociate Medical Director, Clinical Development BraccoAssociate Medical Director, Clinical DevelopmentNeedham, MassachusettsWorking within cross-functional study teams, the role leads medical data and safety review, investigator engagement, study-level interpretation and reporting, and contributes to regulatory activities and program strategy under the direction of the Medical Director. Working knowledge of the clinical development lifecycle, Good Clinical Practice, protocol design, safety surveillance and pharmacovigilance, medical data review, clinical study reporting and clinical content for IND/CTA and marketing-application documentation.
Co-Founder & CEO - AI Clinical Documentation Compliance FutureSight VenturesCo-Founder & CEO - AI Clinical Documentation ComplianceBoston, Massachusetts$80–$85 / hourYou’ll co-create with a proven studio team, led by John Carbrey (4x entrepreneur, $100M ARR), Krista LaRiviere (3x exited, E&Y Top Women Entrepreneur), Alan Smith (Strategyzer co-founder, $120M in products built), Prathna Ramesh (former MD of Maple Leaf Angels, $275M in follow-on capital), and Johnny Tong (0-to-1 builder, acquired by SAP and Stripe) bring a rare combination of operator exits, institutional investing, and AI product depth. The market signal is incredibly strong: Unprompted Product Pull: Every single lead described the exact product we want to build: a pre-billing, real-time, EHR-integrated flagging layer that checks documentation against payer-specific rules before claims are submitted.
Clinical Specialist, Coronary - Boston Abbott LaboratoriesClinical Specialist, Coronary - BostonBoston, MA$61,300–$122,700 / yearEducate customers on the merits and proper clinical usage of company products by giving presentations and demonstrations using a wide variety of formats and platforms (e.g., slides, transparencies, manuals) to keep all customers abreast of the latest product, therapy, and technology developments and current items of interest in the industry. Respond to customer needs and complaints regarding products and service by developing creative and feasible solutions or working with other related personnel (e.g., sales, clinical research, marketing, product development) to develop optimal solutions.
Director, Clinical Scientist Dyne Therapeutics IncDirector, Clinical ScientistWaltham, MA$222,000–$258,000 / yearClinical Data Review, Interpretation & Safety Oversight: Support ongoing patient-level and aggregate clinical data review, including safety, efficacy, biomarker, pharmacodynamic, endpoint, and protocol compliance data, to identify trends, insights, risks, protocol deviations, safety trend review, patient profile review and other potential issues. Strong cross-functional collaboration and influencing skills, with the ability to build alignment across Clinical Development, Clinical Operations, Biostatistics, Data Management, Pharmacovigilance, Regulatory Affairs, Translational Medicine, Medical Affairs, external vendors, and study sites.
Medical Director, Clinical Science, GI2 TAU Takeda Pharmaceutical Co LtdMedical Director, Clinical Science, GI2 TAUCambridge, MA$237,200–$372,790 / yearAssesses scientific, medical, and development feasibility, evaluating strategic fit with overall portfolio, evaluating complete or ongoing clinical trials, assessing regulatory interactions and future development plans, interacting with upper management of potential partner/acquisition companies during DD visits and alliance negotiations, and representing clinical science on internal assessment teams in conjunction with TPNA/TPEU/TPC. These responsibilities include leadership roles in meetings with the regulatory organizations or key opinion leaders, establishment of strategy for assigned compounds, and the direction of clinical scientists involved in developing documents required to outline the Company positions on research programs or regulatory applications (e.g.
Experienced Clinical Project Manager - Inflammation (Sponsor Dedicated/ Remote- US only) Syneos Health IncExperienced Clinical Project Manager - Inflammation (Sponsor Dedicated/ Remote- US only)MARemoteTogether we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Selecting us as an employer secures a career in which you're guaranteed to: Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.
Associate Medical Director, Clinical Development, Ophthalmology Regeneron PharmaceuticalsAssociate Medical Director, Clinical Development, OphthalmologyCambridge, MassachusettsIn this role, you will serve as Medical Lead for clinical trials, designing clinical study concepts and leading the Global Clinical Study Team, while collaborating with discovery teams, the Therapeutic Head, and Strategic Program Teams to deliver high-quality, scientifically sound program milestones. We are seeking a Medical Director, Clinical Development to join our Clinical Development Program (CDP) team, supporting our Ophthalmology therapeutics portfolio.
Manager, Global Clinical Supply Chain Planning Takeda Pharmaceutical Co LtdManager, Global Clinical Supply Chain PlanningBoston, MA$116,000–$182,270 / yearThe Manager, Planning Lead will attend clinical project meetings to gather relevant information, translating clinical trial protocol information into a study supply plan, forecast study product requirements, interacting and negotiation with key project stakeholders to provide delivery timelines and budget. Oversee forecast planning and inventory management of all relevant investigational medicines and comparators for portfolio, leading in matrix of SMEs spanning Takeda supply chain, Takeda pharmaceutical sciences organizations and external partners.