Head of Clinical Sciences Moderna IncHead of Clinical SciencesCambridge, MA$243,100–$437,000 / yearPartner with critical Functional Line Leaders (Study Physicians, Clinical Operations, Data management, Translational medicine, Biometrics, Safety) to define cross-functional ways of working with Clinical Sciences and ensure trials are designed to meet defined Go/No Go criteria, and data generated and interpreted for external presentation, regulatory reporting/filing milestones. This role requires a strong track record of successfully developing biologics from pre-clinical through BLA; a deep understanding of all components of clinical drug development; superb ability to interrogate clinical data and identify signals and patterns; line function/team leadership skills, and a deep commitment to transforming patients' lives.
Senior Principal Investigator, Crypto Asset Investigations - Blockchain Technology Financial Industry Regulatory Authority IncSenior Principal Investigator, Crypto Asset Investigations - Blockchain TechnologyBoston, MA$114,200–$238,300 / yearBoston, MA: $114,200.00 - $238,300.00 Chicago, IL: $125,900.00 - $228,000.00 Denver, CO: $114,200.00 - $207,200.00 Jericho, NY: $114,200.00 - $248,700.00 Jersey City, NJ: $137,000.00 - $248,700.00 New York, NY: $137,000.00 - $248,700.00 Rockville, MD: $131,200.00 - $238,300.00 Tysons, VA: $131,200.00 - $238,300.00 Washington, DC: $131,200.00 - $238,300.00 Woodbridge, NJ: $125,900.00 - $248,700.00 . FINRA employees are required to disclose to FINRA all brokerage accounts that they maintain, and those in which they control trading or have a financial interest (including any trust account of which they are a trustee or beneficiary and all accounts of a spouse, domestic partner or minor child who lives with the employee) and to authorize their broker-dealers to provide FINRA with duplicate statements for all of those accounts.
Supervising Attorney PDD Lowell Committee for Public Counsel ServicesSupervising Attorney PDD LowellLowell, MAThe following attributes are preferred for the position of Supervising Attorney: Significant jury trial experience as lead counsel in criminal cases; including Superior Court cases; Commitment to working with a culturally diverse, low-income population, Willingness and ability to work positively and collaboratively with both the Attorney in Charge and Supervisees; A demonstrated commitment to the principle of zealous advocacy in the representation of indigent persons in criminal cases; Ability and commitment to complete annual performance evaluations in a timely and comprehensive manner; Strong interpersonal and analytical skills; Ability to work in community and defense-oriented capacity, both independently and collaboratively; and, Foreign language skills, Spanish in particular, are desirable. The supervisory duties of the Supervising Attorney include, but are not limited to, the following in accordance with the CPCS Guidelines for Supervision of Public Defender Trial Attorneys and the Guidelines for the Implementation of Unified Public Defender Division Offices: Regular one-on-one meetings with individual supervisees to review case files, as well as group meetings, to review case preparation and performance; In-court supervision, including second-seating of trials and significant pretrial hearings; Preparation of annual performance evaluations; Presentation of in-office training sessions; Supervision of other staff, such as investigators and student interns, as delegated by the office's Attorney in Charge; and, Other duties as assigned.
Fellow in AI/ML for Cellular and Protein Computational Biology Harvard UniversityFellow in AI/ML for Cellular and Protein Computational BiologyCambridge, MAThis role focuses on applying modern AI/ML methods to protein and cellular biology, including protein structure prediction, protein-protein and small-molecule-protein docking, cell state prediction from large-scale Perturb-seq datasets, and multimodal modeling of protein function and cellular state. Bachelor's or master's degree in computer science, statistics, electrical engineering, applied mathematics, computational biology, bioengineering, biophysics, or a related quantitative field required by the expected start date.
Sr. Director Field Medical Excellence & Training, Immunology Celldex Therapeutics IncSr. Director Field Medical Excellence & Training, ImmunologyBoston, MA$203,157–$263,841 / yearThis position plays a critical role in strengthening the capabilities of the Medical Science Liaison (MSL) and home-office medical organizations by integrating scientific knowledge with structured training, data-driven insight generation, and disciplined execution supporting Celldex's growing immunology portfolio and future commercialization efforts. Partnering closely with Medical Affairs leadership, Field Medical leadership, Home Office Medical Affairs, Commercial Field Training, Compliance, HR, and other cross-functional stakeholders, this individual will lead the design and implementation of a comprehensive Field Medical Excellence framework.
Director of Community Standards and Conflict Resolution Berklee College of MusicDirector of Community Standards and Conflict ResolutionBoston, MA$107,000–$120,000 / yearCollaborative Compliance: Partner with the Chief Equity Officer and the Director of Equity and Title IX to run a coordinated, connected, and collaborative approach across both functional areas, ensuring institutional alignment with FERPA, CLERY, and VAWA regulations. System Leadership & Conflict Resolution: Conduct System Management: Provide comprehensive oversight of undergraduate and graduate student conduct functions across all campus environments, including Boston, NYC, Valencia, and Online.
Research Associate/Statistician Harvard UniversityResearch Associate/StatisticianCambridge, MA$65,000–$95,000 / yearThe Choi Lab in the Department of Oral Health Policy and Epidemiology (OHPE) seeks a research associate to join our research team and provide quantitative and analytical support for research projects evaluating the impact of health policies and healthcare delivery models on health outcomes and health disparities. Under the supervision of the principal investigators, duties and responsibilities include but are not limited to: Collaborate on study design, development of analytic plans, statistical analyses, interpretation of results, and preparation of manuscripts and scientific reports.
Fellow in AI/ML for Scientific Applications, Foundation Models, and AI Systems Harvard UniversityFellow in AI/ML for Scientific Applications, Foundation Models, and AI SystemsCambridge, MABachelor's or master's degree in computer science, statistics, electrical engineering, applied mathematics, computational biology/neurobiology, or a related quantitative field required by the expected start date. Demonstrated ability to use modern AI-assisted and agentic coding tools effectively, such as Claude Code, Codex, or similar systems, in research and development workflows.
Rheumatology (Senior) Medical Director - Medical Affairs Swedish Orphan Biovitrum ABRheumatology (Senior) Medical Director - Medical AffairsWaltham, MA$224,000–$290,000 / yearDevelop and foster strong collaborative relationships with internal partners, including Regulatory Affairs, Clinical Operations, Market Access, Medical Information, Pharmacovigilance, Sales, and Marketing, and provide medical insight and product- and disease-state expertise to meet business objectives. Develop a US evidence generation strategy to address stakeholder (HCPs, payers, and patients) needs (including product differentiation, health outcomes), collaborating with HEOR and global partners.
Associate Director, Medical Affairs CSL Behring LLCAssociate Director, Medical AffairsWaltham, MAWorking in close collaboration with cross-functional partners and engaging effectively with external thought leaders, the role helps drive medical and scientific communication, support evidence generation, advance clinical understanding, and strengthen scientific engagement in global markets (US and International). We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.
Clinical Research Coordinator Peregrine TeamClinical Research CoordinatorBoston, MAPeregrine Team is seeking a Clinical Research Coordinator to support clinical trial operations for a leading pharmaceutical organization. Coordinate day-to-day clinical trial activities, including patient scheduling and follow-ups.
Senior Program Manager (Spm) - Mastocytosis SanofiSenior Program Manager (Spm) - MastocytosisCambridge, MA$122,250–$176,583.33 / yearMain Responsibilities: Strategic Partnership & Leadership • Lead program management initiatives for Mastocytosis in strategic partnership with the Medical Program Lead (MPL) • Collaborate with Global Medical Director to operationalize Global Medical Team strategies and deliverables • Drive integrated evidence generation planning through cross-functional partnerships with Global Medical Directors, Brand teams, and functional leads. Operational Excellence & Process Management • Optimize cross-functional communication and decision-making through meeting facilitation and stakeholder engagement • Streamline operational workflows to ensure compliance with internal SOPs and external regulatory guidelines • Utilize harmonized Program Management Tools to manage portfolio-level activities across the Program Management organization.
Senior Clinical Research Director, I&I SanofiSenior Clinical Research Director, I&ICambridge, MA$236,250–$393,750 / yearAs relevant, within a project, ensure leadership, build consensus, coordinate action plans with other CRDs and stakeholders to resolve project-related study issues, anticipates potential issues (sharing lessons learned) across the project or study teams. Provide appropriate medical input & support for all activities related to clinical studies such as medical training, feasibility, medical review of data, medical information for the study team, medical advisors/Clinical Project Leaders from Clinical Study Units, and investigators.
Director, Clinical Science WhoopDirector, Clinical ScienceBoston, MA$220,000–$245,000 / yearAt WHOOP, we view total compensation as the combination of base salary, equity, and benefits, with equity serving as a key differentiator that aligns our employees with the long-term success of the company and allows every member of our corporate team to own part of WHOOP and share in the company's long-term growth and success. You will build and mentor a high-performing team of Clinical Scientists, strengthen WHOOP's clinical science capabilities, and ensure our evidence generation strategy meets the expectations of regulators, clinicians, members, and the business.
Senior Medical Science Liaison - Gene Therapy US Medical Affairs Orchard TherapeuticsSenior Medical Science Liaison - Gene Therapy US Medical AffairsBoston, MARemote$190,000–$240,000 / yearDevelop a territory profile including Centers of Excellence, key expertise, newborn screening approaches and leaders, and market access pathways to inform medical strategy and tactical planning in collaboration with our Commercial, Diagnostic, and Patient Advocacy partners. As a field-based member of the medical affairs team, the Sr MSL will be responsible for developing and enhancing professional relationships with external thought leaders involved in all phases of the clinical development process through a fair-balanced and high-value exchange of clinical and scientific information.
Medical Writer (Remote, US) Getinge GroupMedical Writer (Remote, US)Boston, MARemoteStrong working knowledge of regulations and guidance relating to Clinical Affairs, including EU MDR (2017/745), EU MDD (93/42/EEC), MEDDEV guidance, including 2.7/1 Revision 4 and 2.12/2 Revision 2, relevant MDCG guidance, ISO 14155, ICH guidance including E3 CSR, E6 (R3) GCP, and familiarity regulations/ guideline relating to Risk management (i.e. ISO 13485 and ISO14971). Performs comprehensive systematic, documented literature reviews using various search engines in order to support the Clinical Evaluation, Post-market Clinical Follow-Up, awareness of current State of the Art as well as protocol development and any ad hoc reports required.
NewClinical Research Nurse (PRN) Adams ClinicalClinical Research Nurse (PRN)Watertown, Massachusetts$45,000–$55,000 / yearThis position will also involve general research-related responsibilities like facilitating the informed consent process, administration of screening procedures, data entry, maintenance of regulatory binders, and other nursing functions as required in support of the clinical trial. As a member of our clinical team, you will work under the supervision of our physician principal investigators and clinical nurse manager on the conduct of pharmaceutical-sponsored clinical trials in accordance with FDA regulations and GCP guidelines.
Senior Vice President, Clinical Development Amylyx PharmaceuticalsSenior Vice President, Clinical DevelopmentCambridge, MARemote$416,000–$468,000 / yearThe Senior Vice President (SVP) of Clinical Development will provide strategic direction and technical leadership to the clinical development team, including clinical-regulatory development planning, clinical trial design, implementation and execution, clinical data analysis and management, and clinical competitive intelligence. Overall, the main responsibility will be to provide strategic leadership for the clinical and medical aspects for the various programs and work closely with a cross-functional team to align the clinical development plan with the overall development strategy of the relevant products.
Associate Director, Clinical Quality Compliance Stoke Therapeutics, Inc.Associate Director, Clinical Quality ComplianceBedford, MA$192,000–$215,000 / yearThis person will support Stoke's clinical study teams towards ensuring compliance with global regulations (e.g., FDA, EMA, etc.) and will be required to contribute to developing the right strategies for the design and execution of all Stoke clinical and bioanalytical studies. This person will be responsible for establishing Stokes inspections management program for GCP inspections and expected to be influential towards maturing Stoke's quality culture and help reach a sustained state of inspection readiness.
NewStudy Physician, Medical Director - Neuroimmunology, Immunology, BioPharmaceuticals R&D AstraZeneca PlcStudy Physician, Medical Director - Neuroimmunology, Immunology, BioPharmaceuticals R&DCambridge, MA$241,613–$362,420 / yearContribute medical content and final medical review to clinical sections of study- and program-level documents such as protocols, ICFs, IB, briefing books, BTD, PIPs, SAPs, and safety periodic reports, providing risk-benefit framing and clinical rationale. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles).