Associate Director, HEOR & RWE Les Laboratoires Servier SASAssociate Director, HEOR & RWEBoston, MA$184,000–$218,000 / yearDeep expertise in innovative RWE methodologies required for pipeline assets, including the design of external/synthetic control arms to contextualize single-arm clinical trials and the characterization of unmet medical needs in rare oncology indications. Evidence Generation and Impact Measurement: Oversee the end-to-end delivery of RWE studies (e.g., database analysis, chart reviews, prospective registries) to characterize unmet needs and disease burden in niche solid tumor indications.
Systems Medical Director, Psychiatric Emergency Services Boston Medical CenterSystems Medical Director, Psychiatric Emergency ServicesBoston, MAThis physician leader will provide strategic, administrative, and clinical oversight of Psychiatric Emergency Services across the Boston Medical Center Health System, working in close partnership with leadership from the Departments of Psychiatry and Emergency Medicine. Through its integrated network of hospitals, physicians, and advanced practice providers, the system provides comprehensive care to diverse communities while advancing clinical excellence, education, research, and innovation.
Division Director- Emergency Medicine Boston Children's HospitalDivision Director- Emergency MedicineBoston, MA$132,683.20–$212,295.20 / yearPartners closely with the Division Chief on revenue integrity, physician staffing operations, advanced-practice-provider (APP) program administration, operational analytics, and the division's community-network hospital relationships. Experience: 8+ years of progressively responsible experience in academic clinical and research operations, including professional fee billing/revenue integrity and clinical operations management.
Senior Director Health Economics and Outcomes Research HEOR Vor BioPharma IncSenior Director Health Economics and Outcomes Research HEORBoston, MA$280,000–$310,000 / yearOperating in a resource‑lean, fast‑moving biotech, this leader builds the HEOR function from the ground up, partners cross‑functionally to shape clinical and evidence strategy, and ensures that payers, HTA bodies, clinicians, and patient communities understand the clinical, economic, and humanistic value of the therapy-especially critical in rare or high‑unmet‑need diseases. The Senior Director, HEOR leads the strategy and execution of health economics, real‑world evidence (RWE), and value demonstration activities to support global and US market access for the company's lead asset(s).
Associate Director Biostatistics Alnylam Pharmaceuticals IncAssociate Director BiostatisticsCambridge, MA$185,300–$250,700 / yearThe Associate Director, Biostatistics is responsible for statistical activities in support of clinical trials, including contributing to trial designs, authoring statistical sections of protocols, preparing statistical analysis plans, and reviewing and interpreting the analysis of clinical trial data. Our deep pipeline, late-stage programs, and bold vision reflect our core values: fierce innovation, passion for excellence, purposeful urgency, open culture and commitment to people.
Associate Director, Medical Writing Rhythm Pharmaceuticals IncAssociate Director, Medical WritingBoston, MA$160,000–$240,000 / yearDrive document execution for complex global programs by defining development steps, timelines, resources, review processes, data needs, and cross-functional communications to deliver key documents on time, including protocols, clinical study reports, investigator brochures, regulatory submissions, and response documents. Ensure accuracy and consistency across clinical, medical, regulatory, and pharmacovigilance documents by providing expert review of study- and program-level materials, including regulatory submissions, annual reports and updates, DSURs, PBRERs, posters, and manuscripts.
Sr Medical Director (Heme Oncology) Les Laboratoires Servier SASSr Medical Director (Heme Oncology)Boston, MA$298,000–$350,000 / yearThis executive leadership role is responsible for designing, developing, and executing the strategic Medical Affairs plans to support and maximize the understanding of how these assets bring value to HCP's and patients in an ever changing and competitive clinical landscape while also looking for and capitalizing on lifecycle management opportunities. Collaborate with Medical Science Liaison (MSL) leadership to design impactful scientific training programs, ensuring field teams are equipped to communicate complex Scientific Information on Unapproved Uses (SIUU) or approved indications safely and accurately.
Site Lead and Medical Director - BMC Brighton Boston Medical CenterSite Lead and Medical Director - BMC BrightonBrighton, MAThe Site Lead Physician is a practicing primary care physician who provides clinical and operational leadership for the Boston Medical Center (BMC) Brighton or BMC South adult Primary Care practices of Boston Medical Center Health System (BMCHS). In certain sites and subject to the direction of BMCHS internal medicine residency program leadership, provide guidance and leadership to residents, students and other trainees within the clinic, as well as managing physicians working as preceptors for trainees.
Director, Nonclinical Development Rhythm Pharmaceuticals IncDirector, Nonclinical DevelopmentBoston, MA$182,000–$275,000 / yearPropose, design, and oversee nonclinical toxicology, DMPK, and ADME studies at external CROs (GLP and non‑GLP), providing scientific oversight of protocols, execution, data interpretation, and final reports, and managing CRO relationships, timelines, and budgets. Serve as the nonclinical development lead on cross‑functional program teams, providing scientific input to development strategy, risk assessment, and decision‑making across multiple programs.
Director – Quality GCP Monte Rosa Therapeutics, IncDirector – Quality GCPBoston, MassachusettsFull timeOverview: Monte Rosa Therapeutics is seeking a Director Quality GCP to provide strategic oversight of phase-appropriate Quality GCP and GCLP activities, including GCP quality oversight of ongoing quality activities supporting active pre-clinical and clinical programs through participation on in-house and external cross-functional teams. Responsibilities: Primary GCP Quality contact for identified vendors and investigator sites supporting clinical programs as well as other GCP quality events (e.g., potential serious breach assessments, CAPAs).
Director, Program Management I & I Full Life Cycle Monte Rosa Therapeutics, IncDirector, Program Management I & I Full Life CycleBoston, MassachusettsFull timeAs a core member of the Program Team, the Director will partner closely with Clinical, Regulatory, CMC, Nonclinical, Biomarkers, Translational Sciences, and Commercial leaders to integrate strategy and execution across the full development lifecycle. Overview: The Associate Director of Program Management will serve as a strategic and operational leader for priority immunology and inflammation programs, driving assets from mid- to late-stage development through regulatory submission.
Associate Director, Corporate Communications Monte Rosa Therapeutics, IncAssociate Director, Corporate CommunicationsBoston, MassachusettsFull timeThe ideal candidate combines strong communications expertise with scientific literacy and a solid understanding of the biopharmaceutical sector, allowing this person to translate complex scientific and clinical data into clear and engaging narratives for investors, media, and other key stakeholders. Collaborate with internal stakeholders and external partners, including investor relations advisors, public relations firms, and media contacts, to coordinate consistent and effective corporate messaging.
Director, Drug Safety & Pharmacovigilance (Inflammation & Oncology) Monte Rosa Therapeutics, IncDirector, Drug Safety & Pharmacovigilance (Inflammation & Oncology)Boston, MassachusettsFull timeThis role is responsible for establishing and executing global safety strategy across early‑ and mid‑stage clinical programs, with particular focus on immune‑mediated toxicities, oncology risk management, and complex benefit–risk assessment. Overview: The Director of Drug Safety & Pharmacovigilance provides strategic and hands‑on leadership for pharmacovigilance activities supporting a clinical‑stage biotech pipeline in inflammatory and oncology diseases .
Director of Physician Development HCP TalentDirector of Physician DevelopmentMassachusettsRemoteThis is a ground-floor "hunter" opportunity ideal for an experienced healthcare sales or business development professional who excels at opening doors, building trust with orthopedic surgeons, and navigating complex commercial deals. Identify, prioritize, and target high-volume orthopedic surgeons and private practices across New Hampshire, Connecticut, Maine, and Massachusetts using market data, due-diligence lists, and personal networks.
NewPatient Safety Medical Director Vertex PharmaceuticalsPatient Safety Medical DirectorBoston, Massachusetts$276,000–$414,000 / yearDirectly and/or via oversight of direct reports, the role will lead pre-marketing risk assessment, planning for First-In-Human (FIH) studies, safety content of key Modules (SCS, CLO, Labelling) in regulatory authority submissions for approval, including planning, content and execution of Risk Management Plans (RMPs) and/or Risk Evaluation and Mitigation Strategies (REMS) for and post-marketing requirements. The Senior Medical Director, Patient Safety, Disease Area Safety Head (DASH) will lead all safety and benefit-risk related activities for products within the role's Disease-area and/or Franchise, including pre-franchise products from first in-human clinical trials, into and throughout commercialization.
NewDirector Technical Solutions Alnylam Pharmaceuticals IncDirector Technical SolutionsMA$200,700–$271,500 / yearMinimum 15 years' industry experience (Pharmaceutical, Biotech, CRO) leading technical projects and/or supervising teams to deliver data/analytics solutions; Demonstrated technical expertise with clinical databases, AWS/EDC platforms, data imports/integrations, data analytics platforms and/or data visualization tools; advanced programming and analytical skills using SAS, R and Python an asset. Experience driving data solutions projects or system implementations (i.e., data dashboards, R/SAS/data analytics infrastructure, data warehousing, data visualization and/or risk-based data review tools/systems) with clinical team members; Demonstrated experience working with IT and cross-functional counterparts in evaluating and implementing clinical data systems, constructing technical business requirements, specifications and supporting validation documentation.
Assistant Director, Clin Communication Enhancement - Augmentative Comm Boston Children's HospitalAssistant Director, Clin Communication Enhancement - Augmentative CommWaltham, MA$140,649.60–$225,024.80 / yearFull-time position providing clinical patient care, supervising trainees, and managing clinical services within the Augmentative Communication Programs, including outpatient Augmentative Communication, Inpatient Augmentative Communication, Autism Language, and Jay S. Fishman ALS Augmentative Communication Programs. Provides guidance, instruction, and mentoring to subordinates involved in departmental or professional activities such as continuing education, quality improvement, and development of policies, procedures, and clinical practice guidelines.
Medical Director MedElite Group, LLC.Medical DirectorBoston, MA$200,000–$300,000 / yearInfinite Medical P.C. is a nationwide network of advanced practice providers and specialty clinicians committed to delivering high-quality, proactive care directly to residents in skilled nursing and long-term care facilities. As the Medical Director, you will play a key role in overseeing the delivery of comprehensive care to patients, ensuring high-quality service, and promoting best practices across the healthcare team.
Director, Statistical Programming Kura OncologyDirector, Statistical ProgrammingBoston, MA$234,644–$263,000 / yearMS in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related field with a minimum of 10-12 years of programming experience in the pharmaceutical industry, or BS in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related field with 12+ years of programming experience in the pharmaceutical industry. Kura developed and is commercializing KOMZIFTI® (ziftomenib), the FDA-approved once-daily, oral menin inhibitor for the treatment of adults with relapsed or refractory NPM1-mutated acute myeloid leukemia, and continues to pioneer advancements in menin inhibition and farnesyl transferase inhibition.
Director, Patient Focused Drug Development and Innovation Sarepta Therapeutics IncDirector, Patient Focused Drug Development and InnovationCambridge, MA$185,600–$232,000 / yearReporting directly to the Senior Director, Patient Affairs Strategy and Operations, the Director, Patient Focused Drug Development and Innovation will design and lead strategic collaborations to ensure patient focused drug development across the pipeline and embed the patient voice into R&D decision-making. This role integrates the perspectives of patients and caregivers into the strategic and operational framework of the organization, spanning research and development to develop innovative solutions to support clinical trials that meet the needs of the patient community.