Research Fellow in Global Mental Health Implementation Science Harvard UniversityResearch Fellow in Global Mental Health Implementation ScienceMAResponsibilities: (1) Develop and implement an independent research project that extends and complements the work of the lab; write and submit proposals to fund the research; secure and maintain IRB and regulatory approvals; conduct analysis, publish findings, and disseminate research findings through presentations at conferences and scientific meetings; (2) act as scientific liaison for day-to-day oversight of research activities between Harvard Medical School and the project sites and collaborators, including conducting and leading data analyses across the study components; ability to manage virtual meetings and frequent travel to the project sites is required; (3) design intervention materials, training content, and data collection instruments; and lead the implementation of study protocols; monitor data collection and quality in the field; (4) support capacity building within the team at Harvard Medical School and at the project sites through presenting work to local stakeholders and research collaborators, providing guidance and mentorship to research staff involved in different aspects of the research project, and engaging stakeholders at the study sites and surrounding communities in dissemination of the project findings. In addition to carrying out mental health implementation research, the successful candidate will be expected to apply for fellowship funding, contribute to the writing of grants and manuscripts for peer-reviewed publication, present research findings at conferences and scientific meetings, participate in teaching and mentoring of lab members as needed, and otherwise contribute to overall lab operations in a collaborative environment.
Clinical Research Coordinator II - Lowell General Hospital, Cancer Center - On-site Tufts MedicineClinical Research Coordinator II - Lowell General Hospital, Cancer Center - On-siteLowell, MassachusettsThe Clinical Research Coordinator supports clinical trials by recruiting and screening participants, conducting informed consent, and coordinating all protocol‑required visits, procedures, and follow‑up. Responsible for assisting with Institutional Review Board (IRB) requirements for each study including meeting institutional educational requirements, submitting documents for review, adverse event reporting and annual reviews.
Lynch Family Foundation Health Equity Postdoctoral Research Fellow Harvard UniversityLynch Family Foundation Health Equity Postdoctoral Research FellowBoston, MAApplicants should have experience collaborating with local research partners in low-income communities, demonstrated a capacity for independent work, and be expected to engage with researchers and faculty and participate in activities convened by the department. The aim of this program is to expand the pool of talented academic leaders equipped to conduct research that advances health equity using biosocial, interdisciplinary approaches that are core to social medicine.
U.S. Health Equity Postdoctoral Research Fellow Harvard UniversityU.S. Health Equity Postdoctoral Research FellowBoston, MAPostdoctoral fellows will pursue projects investigating critical issues such as expanding access to care, strengthening health systems, and testing community-based interventions-all with the goal of informing scalable changes that could benefit millions of Americans. Applicants should have experience collaborating with local research partners in low-income communities, demonstrated a capacity for independent work, and will be expected to engage with department faculty and participate in activities convened by the department.
Research Associate Co-Op, Protein Biochemistry Keros TherapeuticsResearch Associate Co-Op, Protein BiochemistryLexington, MA$28–$32 / hourWith 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. Support protein production efforts, including expression in mammalian systems, purification to achieve high quality reagents using FPLC, affinity, ion-exchange, and SEC chromatography, and continuous optimization of production methods for novel biomolecules.
NewRemote Web Research Specialist TuringRemote Web Research SpecialistBoston, MassachusettsRemote$30–$50Turing helps customers in two ways: Working with the world’s leading AI labs to advance frontier model capabilities in thinking, reasoning, coding, agentic behavior, multimodality, multilinguality, STEM and frontier knowledge; and leveraging that work to build real-world AI systems that solve mission-critical priorities for companies. Minimum Qualifications Demonstrated open-web research ability, including locating primary records and navigating government and institutional databases, archives, registries, and PDF documents.
NewResearch Software Engineer ATIResearch Software EngineerWoburn, MAFounded by experienced entrepreneurs and backed by major players in the automotive and tire sectors, ATI is building the next generation of tools that make tire shops and dealership service lanes faster, safer, and smarter. Position Overview: We are seeking a Research Software Engineer to lead the architectural design of our research software ecosystem and serve as the primary bridge to production.
Senior Manager / Site Director, Clinical Operations Adams ClinicalSenior Manager / Site Director, Clinical OperationsWatertown, MassachusettsThe Senior Manager provides site-level leadership and operational ownership of clinical operations, with direct responsibility for staff management, study execution, regulatory compliance, strategic alignment with network leadership, and ensuring high-quality trial execution that meets sponsor expectations and business objectives. The Site Director assumes the same core clinical operations responsibilities while providing broader site-wide leadership through additional support of the Clinical Science function, clinician development, cross-functional performance, and integration of clinical science with site operations in partnership with Clinical Science leadership.
Psychiatric Nurse Practitioner/Physician Assistant Adams ClinicalPsychiatric Nurse Practitioner/Physician AssistantBoston, Massachusetts$125,000–$175,000 / yearIn addition, the Clinician – Medical Rater performs basic trial-related medical tasks—including physical and neurological examinations, review of laboratory reports and ECGs, adverse event (AE) assessment, and concomitant medication review—under the supervision of the PI and/or Sub-I. The Clinician – Medical Rater works closely with a multidisciplinary research team in a fast-paced clinical research environment to support high-quality data collection and successful trial execution.
Assistant Psychedelic Dosing Session Monitor Adams ClinicalAssistant Psychedelic Dosing Session MonitorBoston, Massachusetts$30–$40 / hourWe are seeking a per diem (PRN) Assistant Psychedelic Dosing Monitor to support clinical trials focused on psychedelic research for individuals with depression, anxiety, and other mood disorders at one or more of our research site locations. Minimum of 1 year of experience in a mental healthcare setting including clinical research experience as a Clinical Research Coordinator or in a comparable role supporting psychiatric research studies.
Project Manager - Friedman School of Nutrition Tufts UniversityProject Manager - Friedman School of NutritionBoston, MAWorking closely with the Principal Investigator (PI, Fang Fang Zhang, MD, PhD), research staff, participating clinical sites, and community stakeholders, the Project Manager will oversee day-to-day project operations of a multi-site randomized controlled trial, with primary responsibility for IRB and regulatory coordination, REDCap project development and management, administrative management, purchasing, and financial tracking and reconciliation. The Project Manager will play a central role in supporting a multi-year NIH-funded research study will evaluate whether a Food is Medicine intervention providing medically tailored groceries improves pregnancy outcomes among pregnant women experiencing food insecurity.
Staff Clinical Scientist WhoopStaff Clinical ScientistBoston, MassachusettsRaise the scientific bar across the Clinical organization by mentoring Clinical Scientists and Senior Clinical Scientists, identifying scientific risks and opportunities, and contributing to WHOOP’s longer-term clinical research and evidence-generation roadmap. This role is ideal for an experienced clinical scientist who combines deep expertise in study design, statistics, clinical evidence generation, and scientific communication with the ability to influence strategy across a highly cross-functional organization.
Per Diem Family Nurse Practitioner Or Physician Assistant (Casual Employee) One MedicalPer Diem Family Nurse Practitioner Or Physician Assistant (Casual Employee)Boston, MAOur seamless in-office and 24/7 virtual care services, on-site labs, and programs for preventive care, chronic care management, common illnesses and mental health concerns have been delighting people for the past fifteen years. All regular team members working 24+ hours per week and their dependents are eligible for benefits starting on the team member's date of hire: Taking care of you today.
Per Diem Family Nurse Practitioner or Physician Assistant (Casual Employee) One MedicalPer Diem Family Nurse Practitioner or Physician Assistant (Casual Employee)Boston, MAOur seamless in-office and 24/7 virtual care services, on-site labs, and programs for preventive care, chronic care management, common illnesses and mental health concerns have been delighting people for the past fifteen years. Employee Assistance Program- Free confidential services for team members who need help with stress, anxiety, financial planning, and legal issues.
Per Diem Nurse Practitioner Or Physician Assistant (Casual Employee) One MedicalPer Diem Nurse Practitioner Or Physician Assistant (Casual Employee)Boston, MAOur seamless in-office and 24/7 virtual care services, on-site labs, and programs for preventive care, chronic care management, common illnesses and mental health concerns have been delighting people for the past fifteen years. All regular team members working 24+ hours per week and their dependents are eligible for benefits starting on the team member's date of hire: Taking care of you today.
Per Diem Nurse Practitioner or Physician Assistant (Casual Employee) One MedicalPer Diem Nurse Practitioner or Physician Assistant (Casual Employee)Boston, MAOur seamless in-office and 24/7 virtual care services, on-site labs, and programs for preventive care, chronic care management, common illnesses and mental health concerns have been delighting people for the past fifteen years. Employee Assistance Program- Free confidential services for team members who need help with stress, anxiety, financial planning, and legal issues.
Medical Science Liaison (MSL) Autolus Therapeutics PlcMedical Science Liaison (MSL)MAThrough scientific exchange establish, develop, maintain, and personalise long term professional partnerships with a broad range of external stakeholders including, but not limited to, healthcare professionals, medical experts, investigators, researchers, pharmacists, payers, opinion leaders in key hospitals, institutions, and organizations. Typical activities of an MSL may include, but are not limited to, providing mentoring, guidance and formal field-training to Autolus colleagues, leading high level projects, executing special projects for the MSL Team Leader and representing the at Regional and Global meetings.
Junior Clinical scientist SanofiJunior Clinical scientistCambridge, MA$122,250–$176,583.33 / yearMain responsibilities: Contributes to preparation and/or review of any documents related to the studies and requiring a scientific background (abbreviated protocol/protocol/amended protocol, patient written information, presentations/communication to internal or external partners, study reports, committee charters, protocol registration form, redacted protocol, lay summary …). Contributes to definition of the centralized monitoring strategy in consistency with the planned statistical analysis and is involved in study data validation and review processes, support the CRD for the Clinical Case review (safety events reported to GPV or safety events of special interest), notably to anticipate and prevent last minute queries or backlog and smoothen the process.
Medical Director, Clinical Development, Hepatology GSK plcMedical Director, Clinical Development, HepatologyWaltham, MA$222,750–$371,250 / yearThese responsibilities include some of the following: Contribute to project team discussions on indication planning and incorporate input from across disciplines (scientific, clinical, commercial, regulatory, stats, etc) to support vital deliverables including the Target Product Profile (TPP), clinical development plan (CDP), study protocols, and integrated evidence strategy (IES) and planning. Act as clinical lead for a clinical study, taking a key role on the Study Leadership Team (SLT) and serve as clinical point of contact for a clinical study on the Clinical Matrix Team (CMT), across the internal matrix and a broad range of external experts (e.g., regulators, payors, CROs, consultants, investigators).
Senior Manager, Clinical Program Quality and Excellence (Oncology) 3316 Takeda Development Center AmericasSenior Manager, Clinical Program Quality and Excellence (Oncology)MassachusettsFacilitate investigations into significant quality issues, scientific misconduct and serious breach of GCP; facilitate identification of root cause and development of appropriate corrective and preventive actions; track actions and confirm effectiveness; ensure reporting of potential or confirmed violations to regulatory authorities. Provides quality assurance oversight of the global clinical research programs in Research and Development (R&D), Plasma Derived Therapy (PDT), Vaccines Business Unit (VBU), Oncology Business Unit (OBU) and Global Medical Marketed Products Development (MPD) with the overall goal of inspection readiness.