Clinical Scientist, Associate Director Candel Therapeutics IncClinical Scientist, Associate DirectorNeedham, MA$181,000–$194,000 / yearCandel Therapeutics is seeking an experienced and intellectually curious Clinical Scientist to support our oncology clinical development programs, with an initial focus on prostate cancer and opportunities to contribute across additional solid tumor programs, including lung and brain cancer studies. Author and contribute to key clinical and regulatory documents including Clinical Study Reports (CSRs), Investigator Brochures (IBs), protocols, informed consent forms (ICFs), DSURs, clinical narratives, and IND/BLA regulatory submissions.
Contract Operations Specialist Definium Therapeutics IncContract Operations SpecialistCambridge, MA$75,000–$85,000 / yearSupport contract intake, routing, tracking, execution tracking, contract filing, and signature collection to facilitate efficient contract processing on a variety of agreements, including confidentiality agreements, vendor agreements, consulting agreements, clinical trial agreements, master services agreements, statements of work and amendments. Our lead product candidate, lysergide tartrate (our proprietary orally disintegrating tablet form of lysergide (LSD) D-tartrate), represents a highly differentiated, potential best-in-class opportunity for patients suffering from generalized anxiety, major depressive disorder, and posttraumatic stress disorder.
Clinical Development Medical Director, Hematology Pfizer IncClinical Development Medical Director, HematologyCambridge, MA$239,900–$399,800 / yearCandidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.
Memory Care Center Program Manager Lowell General HospitalMemory Care Center Program ManagerBoston, MA$84,300.22–$107,481.20 / yearThe Memory Care Center Program Manager plays a key role within the Tufts Medicine Memory Care Center and Tufts Alzheimer's Research Program (TARP), helping bring together clinical care, research, and strategic initiatives to improve the experience and outcomes of patients with cognitive disorders and their families. Key areas of focus include supporting Memory Care Center operations; coordinating clinical and research initiatives; advancing dementia screening, assessment, and care pathways; supporting program implementation and performance measurement; and strengthening collaboration across clinical, research, and community partners.
Operations Specialist Getinge ABOperations SpecialistBoston, MAAs an Operations Specialist, you will assume a pivotal role within the Manufacturing and Supply Chain Team, tasked with supporting production scheduling across multiple Contract Manufacturing Organizations, fostering robust communication channels with essential vendors and manufacturing partners, and managing logistics related to product release. Primary responsibilities/authority will include: Production Planning and Scheduling: Collaborate with Manufacturing, Sales Operations, and Commercial Teams to develop accurate production plans and schedules based on demand forecasts, capacity constraints, and inventory targets.
Senior Manager, Trial Master File (TMF) Aura Biosciences IncSenior Manager, Trial Master File (TMF)Brighton, MA$150,000–$185,000 / yearThis role ensures that TMFs - whether managed in-house or by CRO partners - are complete, inspection-ready, and maintained in compliance with ICH-GCP, applicable regulatory requirements, and internal SOPs throughout the trial lifecycle. The Senior Manager, Trial Master File (TMF) is responsible for the strategic oversight, governance, and quality of Aura Biosciences Trial Master Files across the companys clinical trial portfolio.
Referral Operations Manager North Shore Community HealthReferral Operations ManagerSalem, MA$56,400–$70,400 / yearManages the work of the Referral Coordinators - including ensuring that appointments are verified appropriately, referrals are appropriately processed and tracked, and new patients assigned via Community Care Cooperative (C3) are scheduled in a timely manner. North Shore Community Health (NSCH) is a highly accomplished community health organization that prides itself on its compassionate approach to serving the surrounding communities with comprehensive and culturally sensitive care.
Senior Director, Clinical Development Metabolism (MASH) Merck & Co IncSenior Director, Clinical Development Metabolism (MASH)Boston, MA$282,200–$444,200 / yearWork closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; and assist the Executive Director and/or Associate Vice President in ensuring that appropriate Corporate personnel are informed of the progress of studies of our company and competitors' drugs, and of internal and external expert opinion on scientific questions relevant to his/her areas of responsibility. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the Metabolism section of the Atherosclerosis & Metabolism therapeutic area, with a particular focus on MASH (Metabolic Dysfunction-Associated Steatohepatitis) and other obesity-related disorders.
Senior Cloud Operations Engineer, Deployments PegasystemsSenior Cloud Operations Engineer, DeploymentsWaltham, MA$102,400–$153,200 / yearAt Pega, in this position, the technologies you will lead with include Pega Cloud hosted on multi-cloud platforms (AWS, GCP), Microservices (Kubernetes, Docker), Databases (PostgreSQL, MongoDB, Cassandra), Migration Tooling (AWS DMS, GCP DMS), GenAI (Azure OpenAI, AWS Bedrock, GCP Gemini), Observability (Grafana), etc. You are skilled in Cloud Technologies, and have accomplished the below: + 5+ years of executing technical projects with experience navigating technical dependencies, stakeholder alignment, resource management, operational readiness, project progress reporting and cross-team delivery in a global environment.
Enterprise Digital System Clinical Lead - Pathology (Clinical & Laboratory Workflows) Brigham and Women's HospitalEnterprise Digital System Clinical Lead - Pathology (Clinical & Laboratory Workflows)Somerville, MA$75,000–$150,000 / yearThe Enterprise Digital System Clinical Lead- Pathology provides clinical informatics leadership for Epic systems supporting laboratory (Beaker- AP/CP) and non-laboratory clinical workflows related to pathology across ambulatory and inpatient settings. The role includes ownership of highly variable and cross-setting workflows, including ambulatory, inpatient, procedural, and specialty diagnostic pathways, requiring coordination across clinical care teams, laboratory operations, and external partners.
Associate Director, Clinical Quality Assurance Centessa Pharmaceuticals, LLCAssociate Director, Clinical Quality AssuranceBoston, MA$140,000–$180,000 / yearCentessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and Company, is a clinical-stage company developing orexin receptor 2 (OX2R) agonists as a new class of medicines for the treatment of narcolepsy and potentially other sleep-wake disorders. Centessa's OX2R agonist portfolio includes additional clinical and preclinical-stage assets with potential utility across a broader range of neurological, neurodegenerative, and neuropsychiatric conditions.
Associate Director, Clinical Supply Chain Alkermes PlcAssociate Director, Clinical Supply ChainWaltham, MAServing as the primary point of contact, the Associate Director collaborates closely with Clinical Operations, Regulatory Affairs, Quality, Internal & External Manufacturing, and other Clinical Supply Chain personnel, leading complex supply activities that often require multinational coordination. In 2024 and 2025, we were certified as a Great Place to Work in the U.S. and named one of Massachusetts' Top Places to Work by the Boston Globe, a Best Place to Work in Greater Cincinnati by the Cincinnati Business Courier and recognized as a Best Place to Work in BioPharma by Fortune Magazine.
Paralegal And Legal & Compliance Operations Manager bluebird bio, Inc.Paralegal And Legal & Compliance Operations ManagerSomerville, MA$120,000–$155,000 / yearDemonstrated experience in the pharmaceutical, biotechnology, or medical device industry, with working knowledge of the federal Anti-Kickback Statute, the False Claims Act, the Physician Payments Sunshine Act, the PhRMA Code, and Office of Inspector General compliance program guidance. Serve as day-to-day administrator of the contract lifecycle management system, including intake triage, routing, template selection, version control, execution through the electronic signature platform, and post-execution filing and obligation tracking.
Health PBM Operations Manager (Specialty Pharma, PBM) Accenture PlcHealth PBM Operations Manager (Specialty Pharma, PBM)Boston, MALead with the Best: Join an industry-recognized healthcare consulting leader with a global team of over 20,000 professionals, collaborating to drive large-scale healthcare transformation across the globe. Continuous Learning & Growth: Take advantage of unmatched professional development opportunities, including interactive courses, real-world client simulations, and ongoing mentoring, to expand your healthcare consulting expertise.
Business Operations & Analytics Manager GTT, LLCBusiness Operations & Analytics ManagerBoston, MAThe Business Operations & Analytics Manager serves as a key partner to Sterile Processing and Clinical Support Services leadership, helping ensure the department operates efficiently while providing the data and insights needed to drive performance. The ideal candidate enjoys both operational problem-solving and storytelling through data and is equally comfortable managing workforce processes as they are translating complex information into actionable insights.
Associate Director or Director, Clinical Scientist Kymera Therapeutics IncAssociate Director or Director, Clinical ScientistWatertown, MA$160,000–$275,000 / yearHaving advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Skills and experience you'll bring: Bachelor's or advanced degree (MSc, PharmD, PhD) in Life Sciences or related field and 8+ years in pharmaceutical clinical drug development, with experience in global clinical trials and program execution.
Senior Manager, Veeva Regulatory & Data Scholar RockSenior Manager, Veeva Regulatory & DataCambridge, MAReporting to the Senior Director, Commercial & Data, the Senior Manager partners closely with business stakeholders, Quality and Validation, Cybersecurity, Data & Analytics, Infrastructure & Cloud, and external technology partners to translate business priorities into scalable, secure, compliant, and sustainable technology solutions. The Senior Manager leads solution delivery from requirements and design through implementation and ongoing support, maintains sufficient hands-on expertise to independently assess, configure, and troubleshoot complex Veeva solutions, and ensures internal and external delivery teams provide reliable, high-quality services.
Enterprise Digital Systems Clinical Lead - Ambulatory Pathology (Beaker AP/CP) Brigham and Women's HospitalEnterprise Digital Systems Clinical Lead - Ambulatory Pathology (Beaker AP/CP)Somerville, MAThe Enterprise Digital System Clinical Lead - Ambulatory Pathology provides clinical informatics leadership for Epic systems supporting laboratory (Beaker - AP/CP) and non-laboratory clinical workflows related to pathology across ambulatory settings. The role includes ownership of highly variable and cross-setting workflows, including ambulatory and specialty diagnostic pathways, requiring coordination across clinical care teams, laboratory operations, and external partners.
Associate Director, Program Manager Third Rock Ventures LLCAssociate Director, Program ManagerBoston, MA$180,000–$205,000 / yearDevelop and maintain integrated development plans, timelines, milestones, risks, and scenarios in partnership with the Program Leader, functional leaders, and program team members across Clinical Development, Clinical Operations, Regulatory, Technical Operations (CMC), and Nonclinical Development. Reporting to the Director of Program Management, this role partners with the Program Leader and the cross-functional program team - Clinical Development, Clinical Operations, Regulatory, Technical Operations (CMC), and Nonclinical Development - to deliver program milestones on time in a high-functioning program team environment.
Behavioral Health Clinical Site Director Fidelia Counseling ServicesBehavioral Health Clinical Site DirectorWoburn, MassachusettsOur Mission Fidelia Counseling Services’ mission is to provide clinically and culturally effective mental health prevention and intervention services to all in the community, especially at risk children, adolescents, adults and families. Qualifications Education: A Master's degree in a mental health-related field (e.g., Social Work, Counseling) or Healthcare Administration, Business Administration, or a related field is strongly preferred.