Sr. Medical Director, Clinical Development (Psychiatry) AlkermesSr. Medical Director, Clinical Development (Psychiatry)Waltham, MARemote$340,000–$360,000 / yearThis position will work cross-functionally to ensure projects are coordinated with partners from multiple departments within Alkermes including regulatory, preclinical research, clinical pharmacology, translational medicine, toxicology, CMC, new product planning, project management, patient engagement, health economics, legal, finance, medical affairs and commercial. 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.
Medical Director, Clinical Development (Neurology) AlkermesMedical Director, Clinical Development (Neurology)Waltham, MARemote$286,000–$310,000 / yearThis position will work cross-functionally to ensure projects are coordinated with partners from multiple departments within Alkermes including regulatory, preclinical research, clinical pharmacology, translational medicine, toxicology, CMC, new product planning, project management, patient engagement, health economics, legal, finance, medical affairs and commercial. 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.
Executive Medical Director, Clinical Development (Psychiatry) AlkermesExecutive Medical Director, Clinical Development (Psychiatry)Waltham, MARemote$360,000–$390,000 / yearThis position will work cross-functionally to ensure projects are coordinated with partners from multiple departments within Alkermes including regulatory, preclinical research, clinical pharmacology, translational medicine, toxicology, CMC, new product planning, project management, patient engagement, health economics, legal, finance, medical affairs and commercial. Additionally, the Executive Medical Director will participate in internal strategy regarding future therapeutic priorities and interact externally with key global regulatory authorities, industry and scientific organizations, as well as external key thought leaders.
Senior Director, Immunology Clinical Research CSL BehringSenior Director, Immunology Clinical ResearchWaltham, MA$338,000–$390,000 / yearPartnering day-to-day with the Research Therapeutic Area Lead and bench scientists, you will roll up your sleeves to prioritize therapeutic targets, shape clinical development plans, and directly translate mechanistic and preclinical data into first-in-class or best-in-class immunology therapies. Represent CSL Behring at key scientific conferences, advisory boards, and KOL meetings; build and actively maintain a hands-on network of thought leaders, clinical investigators, and academic collaborators.
Clinical Trials Senior Monitor Dana-Farber Cancer Institute IncClinical Trials Senior MonitorBrookline, MARemote$98,900–$108,400 / yearThe Clinical Trials Monitor helps to ensure compliance of the clinical research enterprise with all related regulatory policies and guidelines, including federal, state, local, as well as the policies and procedures outlined by the Dana-Farber Cancer Institute and Dana-Farber Harvard Cancer Center (DF/HCC) consortium. Under the direction of Clinical Trials Office Leadership, s/he will assist in the design, development, implementation, and conduct of an effective monitoring program in accordance with Good Clinical Practice, institutional policies and procedures, and research protocols.
Senior Clinical Trial Manager Korro BioSenior Clinical Trial ManagerCambridge, MA$163,333–$186,667 / yearThis individual will use outstanding cross-functional skills to achieve study and program goals and will develop a solid understanding of the clinical indications being pursued including knowledge of the patient needs, development plan, applicable regulatory guidance as well as the competitive landscape in the therapeutic space. Key Responsibilities: Plan, drive and oversee all aspects of multi-center global clinical trials in compliance with GCPs, SOPs, and within designated program budgets and timelines in close collaborations with key stakeholders and Clinical Research Organizations (CROs).
Postdoctoral Research Fellow Brigham and Women's HospitalPostdoctoral Research FellowBelmont, MAWe are seeking a highly motivated Postdoctoral Research Fellow in Clinical Psychology to join an NIH-funded clinical research study focused on the treatment of posttraumatic stress disorder (PTSD). The position involves direct interaction with research participants with PTSD and requires professionalism, reliability, careful adherence to treatment protocols, and collaboration with the study's clinical and research teams.
Clinical Operations Senior Manager Kiniksa PharmaceuticalClinical Operations Senior ManagerLexington, MAYou will join a dynamic Clinical Operations team working in a fast-paced, highly collaborative environment, with the opportunity to help shape how we deliver high-quality clinical programs and contribute to the future success of the organization. The Senior Manager, Clinical Operations provides / supports the operational leadership and strategic oversight of the planning, conduct, and delivery of global clinical trials.
Associate Director, Clinical Pharmacology City TherapeuticsAssociate Director, Clinical PharmacologyCambridge, MassachusettsThe successful candidate will work in a highly cross-functional environment, partnering closely with Clinical Development, Regulatory Affairs, Clinical Operations, Biostatistics, Data Science, CMC and external collaborators to drive data-driven decision making and advance clinical development. Lead and execute model-informed drug development (MIDD) activities, including population PK, exposure-response, PBPK, and mechanistic PK/PD modeling, either independently or in collaboration with quantitative scientists, to support regulatory interactions and development planning.
Associate Director, Clinical Operations – Therapeutics/Oncology ModernaTXAssociate Director, Clinical Operations – Therapeutics/OncologyCambridge, MassachusettsWe 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. This position will be responsible for initiating and leading clinical trials across all phases, including overseeing CROs and vendors and working cross-functionally on clinical operations strategy and related initiatives.
Senior Director, In-Vivo & Non-Clinical Pharmacology, Research Business Insights & Technology Bristol-Myers Squibb CoSenior Director, In-Vivo & Non-Clinical Pharmacology, Research Business Insights & TechnologyMA$252,640–$306,137 / yearThis leader will partner deeply with Research leadership and the Pharmacology, DMPK, Toxicology, and Translational Science units to deliver the applications, workflow capabilities, AI, and supporting data flows that enable non-clinical decisions across in-vivo biology, DMPK, ADME, non-clinical safety, toxicology, and bioanalytical science. Reporting to the Vice President, Research Business Insights & Technology, this leader will operate as part of a unified BI&T leadership team and act as a trusted partner to Research leadership, translating scientific needs into scalable, integrated technology solutions.
Postdoctoral Research Fellow (Inflammation and Immunology) Lahey Hospital and Medical CenterPostdoctoral Research Fellow (Inflammation and Immunology)Boston, MA$60,000–$75,564 / year0-1 year of postdoctoral research experience in academic or industrial lab setting, and/or teaching assistantship in a university setting, and/or residency, and/or clinical duties beyond that of the qualifying doctoral degree. Problem Solving: Ability to address problems that are varied, requiring analysis or interpretation of the situation using direct observation, knowledge and skills based on general precedents.
Senior Director, Health Economics & Outcomes Research (HEOR) Tetraphase Pharmaceuticals IncSenior Director, Health Economics & Outcomes Research (HEOR)Waltham, MAXACDURO (sulbactam for injection; durlobactam for injection) is a new treatment designed specifically to treat hospital-acquired bacterial pneumonia (HABP) and ventilator-associated bacterial pneumonia (VABP) caused by susceptible strains of bacteria called Acinetobacter baumannii-calcoaceticus complex in adults. ZEVTERA (ceftobiprole) is an approved advanced-generation cephalosporin antibiotic and the only FDA-approved cephalosporin specifically designed to treat adult patients with Staphylococcus aureus bloodstream infections (bacteremia) including those with right-sided infective endocarditis.
Research Associate II, Preclinical Manufacturing Sail BiomedicinesResearch Associate II, Preclinical ManufacturingCambridge, MA$75,000–$100,000 / yearSail’s platform combines first-in-class programmable circular RNA technology (Endless RNA or eRNA), and an industry-leading platform of programmable nanoparticles, utilizing natural components, to unlock comprehensive programming of medicines for the first time. By leveraging cutting-edge eRNA and nanoparticle deployment technology, Sail is also making unparalleled use of AI techniques to identify and design fully programmable medicines that are potent, targeted, versatile, and tunable.
NewJunior Project Planner Clinical Science Medicine Boston UniversityJunior Project Planner Clinical Science MedicineBoston, MAWill maintain all databases of research, conduct literature and other interne-based searches ensuring research is current and compliant, conduct chart reviews and extract pertinent information, review and edit all reports, posters, manuscripts and presentations ensuring all information conveyed is accurate. Will develop and draft research protocols of studies, compile and submit new grant proposals ensuring continued funding, compile, draft and submit IRB and other required documentation to ensure research efforts are compliant.
Pediatric Clinical Social Worker - LICSW Lowell General HospitalPediatric Clinical Social Worker - LICSWBoston, MA$60,908.12–$76,140.43 / yearIn addition, this role focuses on performing the following Social Work duties: Provides social work assistance to patients and families relating to illness, disease, hospitalization and life events in all areas of service as a member of multi-disciplinary team and in liaison with community resources. Clinically assess the patient's needs for long-term care, evaluate the home and family situation, help the patient and family to develop an in-home care plan, explore alternatives to in-home care and arrange for placement if necessary.
2027 Future Talent Program - Discovery Chemistry & Process Research - Intern Merck & Co Inc2027 Future Talent Program - Discovery Chemistry & Process Research - InternBoston, MAIn addition to the discovery and development of synthetic routes to potential drug candidates, interns may engage in high-throughput and data-rich experimentation (HTE/DRE), bio- and chemocatalysis screening and development, laboratory automation, flow chemistry, labeled compound synthesis, involving data science/informatics approaches to reaction optimization and process understanding. Our company's Research Lab's Discovery and Process Research Departments across multiple geographies are seeking summer interns with a passion for scientific research, strong academic performance, communication skills, and the ability to work on cross-functional teams.
Clinical Trial Manager Kailera TherapeuticsClinical Trial ManagerWaltham, Massachusetts$127,000–$155,000 / yearPerform as the lead interface with the CRO regarding status of project activities and deliverables (including but not limited to site identification and selection, pre-study activities, enrollment, management/conduct, database lock, post-study activities). Collaborate with the cross-functional clinical trial team to review and prepare various clinical study documents including but not limited to study protocol, model informed consent forms, and study plans.
Director, Clinical Data Management Kailera TherapeuticsDirector, Clinical Data ManagementWaltham, Massachusetts$196,000–$240,000 / yearProven track record providing strategic data management leadership across late-stage development programs, ensuring data integrity, data quality, and inspection readiness. Strong command of electronic data capture (EDC) systems and clinical data warehousing technologies, with experience across a range of clinical data management platforms.
NewSenior Manager, Clinical Data Management Generate Biomedicines IncSenior Manager, Clinical Data ManagementMA$140,000–$196,000 / yearProvide hands-on oversight of Medidata Rave EDC database builds, including eCRFs, edit checks, custom functions, workflows, and related configuration; create, run, review, and interpret Rave reports and listings to support data review, cleaning, reconciliation, and oversight. The Role: The Senior Manager, Clinical Data Management will serve as the lead data manager for one or more clinical studies or programs, providing strategic and operational oversight of study-level data management activities from study start-up through database lock.