Sr. Director, Clinical Scientist Replimune Group, Inc.Sr. Director, Clinical ScientistWoburn, MA$256,500–$332,000 / yearThe Senior Director, Clinical Development/Clinical Scientist will report to the VP or Executive Director, of the Early Clinical Development team to ensure the successful execution of clinical development programs and deliverables in partnership across the organization, with external vendors, and with external academicians and collaboration partners. The RPx platform is designed to have a unique dual local and systemic activity consisting of direct selective virus-mediated killing of the tumor resulting in the release of tumor derived antigens and altering of the tumor microenvironment to ignite a strong and durable systemic response.
Program Director, Clinical Stabilization Services DimockProgram Director, Clinical Stabilization ServicesBoston, MAFull timeProgram Director, Clinical Stabilization ServicesSummary/ObjectiveThe Program Director, Clinical Stabilization Services (CSS), is responsible for the strategic, clinical, operational, regulatory, and financial oversight of Dimock's BSAS-licensed Clinical Stabilization Services program. Reporting directly to the Chief Behavioral Health Officer, the Program Director provides leadership to multidisciplinary teams and ensures the delivery of trauma-informed, recovery-oriented, person-centered care.
Sr. In-house Clinical Research Associate Alira HealthSr. In-house Clinical Research AssociateFramingham, MassachusettsIn-house CRAs work closely with field CRAs and Clinical Project Managers to ensure the integrity of the trial data without the need for frequent travel. The final offer will be determined within the applicable location-specific range and will depend on the candidate’s confirmed work location, relevant experience, skills, qualifications, internal equity, and role scope.
Regulatory Coordinator Tufts MedicineRegulatory CoordinatorBoston, MA$21.53–$26.91 / hourIn addition, this role focuses on performing the following Administration Project Management duties: Serves as a liaison between the general project management office and the team members engaging in planning, reviews the status of projects and budgets, manages schedules, prepares status reports, and assesses project issues and develops resolutions to meet productivity, quality, and client-satisfaction. Works collaboratively with a variety of personnel at all levels, including faculty and study team members of the Neely Center for Cancer Clinical Research (NCCCR) and external institutions, cooperative groups, clinical trials experts, representatives from the pharmaceutical industry, federal agencies, and other research organizations.
Senior Medical Director, Psychiatry Rapport Therapeutics IncSenior Medical Director, PsychiatryBoston, MA$285,000–$350,000 / yearProven clinical development strategist with hands-on experience of designing, implementing, and conducting clinical trials in neurology, Phase 2a - Phase 3. Working knowledge of psychiatry indications is required, with proven ability to interpret, discuss and present efficacy and safety data relating to clinical trial(s) and proven ability to understand and interpret basic and clinical scientific research reports. Working closely with functional partners (Clinical Operations, Data Management, Biostatistics, Regulatory, Medical Affairs) to ensure an integrated and strategic approach to flawless execution and systematic oversight of study protocols.
Principal Medical Writer Merck & Co IncPrincipal Medical WriterBoston, MA$142,400–$224,100 / yearThe Principal Medical Writer, in partnership with a project lead, leverages strategic and scientific expertise to develop, author, edit, and lead the review of accurate, clear, and compliant clinical, regulatory, and/or public‑facing documents, across multiple programs and therapeutic areas, in support of the company portfolio. In this role, the Principal Medical Writer: Is recognized as a subject matter expert in the design, planning, authoring, editing, and review of accurate, clear, high-quality documents that reflect applicable medical writing best practices (e.g., lean writing, health literacy) and evolving regulatory requirements.
NewSenior Director, Clinical Operations Keros TherapeuticsSenior Director, Clinical OperationsLexington, MA$253,000–$300,000 / yearWith a focus on developing differentiated product candidates that are designed to alter TGF- signaling, we aim to target the pathways critical for the growth, repair and maintenance of blood cells and a number of tissues, including bone, skeletal muscle, adipose and heart tissue. As the leader of the cross-functional Clinical Program Team, the Senior Director Clinical Operations (SDCO) will lead the planning and execution strategy of assigned clinical trials to achieve overall program and corporate objectives.
Associate Director, Clinical Data Management Beeline MedicinesAssociate Director, Clinical Data ManagementBoston, MassachusettsThe Associate Director, Clinical Data Management Leads clinical data management activities across one or more clinical programs, ensuring the timely delivery of high-quality, audit-ready clinical trial data in support of regulatory submissions and clinical development timelines. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully.
Associate Director Drug Product Technical Operations Vor Biopharma Inc.Associate Director Drug Product Technical OperationsBoston, MA$170,000–$195,000 / yearDrug Product and Combination Product Integration: Partner closely with the Combination Product Development Lead to ensure alignment between drug product characteristics, primary container systems, prefilled syringes, needle safety devices, autoinjectors, fill-finish processes, device performance, and product presentation requirements. This role will have end-to-end accountability for drug product manufacturing from late-stage development through commercialization, including manufacturing strategy, technology transfer, aseptic fill-finish, process validation, lifecycle management, commercial readiness, and Drug Product Module 3 content.
Senior Scientist, Translational Research (Oncology TRC) Bristol-Myers Squibb CoSenior Scientist, Translational Research (Oncology TRC)MA$142,220–$172,340 / yearExperience performing biomarker-focused laboratory work, including handling cell cultures and performing analysis of protein and DNA/RNA samples using a variety of methodologies including but not limited to MSD/ELISA, Luminex, RNAi, CRISPR, qPCR and primary cell isolation, culture and functional assays is highly desired. Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
Associate Director, Talent Acquisition Operations & Programs Dyne TherapeuticsAssociate Director, Talent Acquisition Operations & ProgramsWaltham, MAThe Associate Director partners closely with Talent Acquisition, Human Resources, Finance, Legal, IT, Communications, and business leaders to translate hiring priorities into effective execution, drive process improvement, and support a high-quality, data-informed recruiting experience across Dyne. Own and evolve Dyne’s core Talent Acquisition programs, including candidate experience, structured interviewing and assessment, hiring manager and hiring team enablement, recruiter enablement, referral programs, early talent programs, and extended workforce-related TA processes.
Clinical/Development - Senior Research Associate LanceSoft IncClinical/Development - Senior Research AssociateCambridge, MA$45.16 / hourSenior Research Associate, RNASEQ/RLD Support various transcriptomics studies via bulk, small RNA, long read, single cell, spatial and other platforms. Execute day-to-day operations for RNASeq sample preparation, including: RNA isolation, library preparation, QC and sequencing.
Manager, Clinical Supply Chain Centessa Pharmaceuticals, LLCManager, Clinical Supply ChainBoston, MA$90,000–$215,000 / 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. Reporting to the Senior Director, Clinical Supply Chain, the individual will build strong relationships with internal teams and third-party suppliers to align objectives and support successful trial execution, with particular attention to clinical forecasts, inventory systems, and IRT tools.
Sr. Director, Clinical Scientist ReplimuneSr. Director, Clinical ScientistWoburn, Massachusetts$256,500–$332,000 / yearThe Senior Director, Clinical Development/Clinical Scientist will report to the VP or Executive Director, of the Early Clinical Development team to ensure the successful execution of clinical development programs and deliverables in partnership across the organization, with external vendors, and with external academicians and collaboration partners. The RPx platform is designed to have a unique dual local and systemic activity consisting of direct selective virus-mediated killing of the tumor resulting in the release of tumor derived antigens and altering of the tumor microenvironment to ignite a strong and durable systemic response.
Intake Manager, Hospice AccentCare, Inc.Intake Manager, HospiceNorwood, Massachusetts$67,000–$73,000 / yearWe’re proud to be named one of America’s Greatest Workplaces 2025 by Newsweek — a reflection of our shared commitment to excellence, integrity and compassion as we shape the future of aging in place. Work cross-functionally with Director-Clinical Operations (DCO), Team Directors (TD) and DBD to ensure promised services are provided.
Advanced Practice Manager, Neonatology- Full time, Rotating Lahey Hospital and Medical CenterAdvanced Practice Manager, Neonatology- Full time, RotatingBoston, MA$180,003.20–$270,004.80 / yearThe NICU utilizes a collaborative, family-centered care model that brings together advanced practice providers, physicians, nurses, therapists, pharmacists, social workers, and other specialists to provide exceptional care to critically ill and premature infants. As the Advanced Practice Manager, Neonatology, you will provide both clinical and administrative leadership for the NICU Advanced Practice Provider team, consisting of 18 Advanced Practice Providers.
Clinical Patient Advocate - Milford Regional 40 hours, Days UMass Memorial Health Care IncClinical Patient Advocate - Milford Regional 40 hours, DaysMilford, MA$91,312–$164,361.60 / yearResponsible for oversight of patient grievances and organizing the behavioral, nursing, operational and medical reviews which includes collaboration with physician leadership, hospital leadership, patient safety, quality improvement and risk management. Position Qualifications: License/Certification/Education: Required: Active licensure in a clinical healthcare profession (e.g., RN, LPN, LICSW, Respiratory Therapist, Physical Therapist, or equivalent), with demonstrated experience in patient care, care coordination, and interdisciplinary collaboration.
Clinical Director Overstory HealthClinical DirectorBoston, MassachusettsOverstory Health is a newly launched startup building world-class, patient-centric Partial Hospitalization (PHP) and Intensive Outpatient (IOP) programs for individuals with high-acuity mental health needs. With a clinical model validated by McLean Hospital, we provide comprehensive psychiatric, therapeutic, and community reintegration services that help individuals achieve stability, connection, and confidence both during and after the program.
Clinical Trial Manager Repertoire Immune MedicinesClinical Trial ManagerWatertown, MAFull timeThe DECODE platform has been validated through four strategic partnerships with leading pharmaceutical companies—Bristol Myers Squibb, Genentech, Eli Lilly, and Pfizer—representing over $4.5 billion in disclosed total deal value and $185 million in upfront payments received to date. Manage outsourced activities with CROs and vendors (e.g., biomarker and specialty labs), including oversight of performance, compliance with ICH/GCP and SOPs, development of oversight plans, and review of monitoring reports to maintain trial quality and compliance.
Security Operations Analyst ANDURIL INDUSTRIESSecurity Operations AnalystBoston, MA$129,000–$171,000 / yearProactively collaborate with a wide range of stakeholders, guiding detection and response maturity of key worlds, leading incidents and large-scale data baselines, and being responsible with mentoring and guiding junior analysts. To ensure your safety and help you navigate your job search with confidence, please keep the following critical points in mind: No Financial Requests: Anduril will never solicit payment or demand personal financial details (such as banking information, credit card numbers, or social security numbers) at any stage of our hiring process.