154 Results for

Investigator Jobs in Chestnut Hill, MA

Jobs

Rapid Intervention & Survival Skills Instructional Assistant Program Coordinator Commonwealth of Massachusetts

Stow, MA

Instructors/Lecturers/Trainers'',''Instructors/Lecturers/Trainers'',''United States-Massachusetts-Stow-State Road'',''United States-Massachusetts-Stow-State Road'',''Training and Development'',''Training and Development'',''Department of Fire Services'',''Department of Fire Services'',''Part-time'',''Part-time'',''Multiple'',''Multiple'',''Jul 31, 2026, 10:31:30 AM'',''Jul 31, 2026, 10:31:30 AM'',''1'',''1'',''54.39'',''54.39'',''54.39'',''Hourly'',''Mary Travers'',''Mary Travers'',''9785673145'',''Non'',''Non'',''No'',''No'',''Yes'',''Yes'',''false'',''1089290'',''1089290'',''true'',''1089290'',''false'',''Submission for the position: Rapid Intervention & Survival Skills Instructional Assistant Program Coordinator - (Job Number: 260004ZQ)'',''false'',''1089290'',''false'',''true''.

8 days ago

Supervising Attorney - PDD Framingham Commonwealth of Massachusetts

Framingham, MA

The 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. '',''Supervising Staff Attorney-CPC'',''Supervising Staff Attorney-CPC'',''United States-Massachusetts-Framingham - 298 Howard Street'',''United States-Massachusetts-Framingham - 298 Howard Street'',''Legal Services'',''Legal Services'',''Committee for Pub Counsel Srvc'',''Committee for Pub Counsel Srvc'',''Full-time'',''Full-time'',''Day'',''Day'',''Aug 7, 2026, 12:50:15 PM'',''Aug 7, 2026, 12:50:15 PM'',''2'',''2'',''146,988.00'',''100,091.00'',''146,988.00'',''Yearly'',''Sandra DeBow-Huang'',''Sandra DeBow-Huang'',''6174826212'','''','''','''','''',''Yes'',''Yes'',''false'',''1090436'',''1090436'',''true'',''1090436'',''false'',''Submission for the position: Supervising Attorney - PDD Framingham - (Job Number: 260005HJ)'',''false'',''1090436'',''false'',''true''.

1 day ago

Lead Administrative Assistant - Public Defender Division Administration Commonwealth of Massachusetts

Boston, MA

Admin Assistant IV -CPC'',''Admin Assistant IV -CPC'',''United States-Massachusetts-Boston - 75 Federal Street'',''United States-Massachusetts-Boston - 75 Federal Street'',''Legal Services'',''Legal Services'',''Committee for Pub Counsel Srvc'',''Committee for Pub Counsel Srvc'',''Full-time'',''Full-time'',''Day'',''Day'',''Jul 29, 2026, 3:21:24 PM'',''Jul 29, 2026, 3:21:24 PM'',''1'',''1'',''96,855.00'',''65,953.00'',''96,855.00'',''Yearly'',''Sandra Applicants must have: Associate's degree in a related area; at least four years of experience as an administrative assistant or office manager; executive level secretarial skills; or an equivalent combination of education, experience, and skills; and, Access to an automobile in order to travel to offices and other locations that are not easily accessible by public transportation; and, Access to home internet access sufficient to work remotely.

10 days ago

Director of Scientific Communications & Evidence Generation Genetix Biotherapeutics Inc

Somerville, MA

$225,000–$255,000 / year

Position Summary: The Director of Scientific Communications & Evidence Generation will be responsible for developing a plan for disseminating the company's scientific data (manuscripts, abstracts, posters, presentations); as well as identifying clinical evidence gaps, overseeing non-registrational research, and collaborating with cross-functional teams to generate real-world evidence (RWE), health economics and outcomes research (HEOR), and investigator-sponsored research (ISR) to support product value and safety profiles. Data Generation: Lead the development of an integrated evidence generation plan (IEGP) aligned with overall medical affairs goals to address unmet needs in collaboration with Clinical Development, Regulatory, HEOR, and Commercial teams to avoid duplicative efforts.

24 days ago

Clinical Trial Manager Prometrika LLC

Cambridge, MA

Experience working in cross-functional teams and direct involvement in protocol and CRF development is highly valued Proven track record of ensuring GCP/regulatory/protocol compliance, managing timelines and budgets, leading risk assessments, and implementing CAPAs and KPIs SKILLS Working knowledge of the clinical drug development process Strong knowledge of clinical research operations, including interpretation and implementation of FDA regulations/ICH guidelines Strong analytical and problem-solving skills Written, verbal communication and presentation skills in small and large group settings Must possess excellent interpersonal skills Mentoring/coaching Ability to effectively multi-task and prioritize Organizational skills and attention to detail required Solid computer skills requirement of MS applications including (but not limited to) MS Project, Word, Excel, PowerPoint Cross functional and cross-cultural awareness Ability to work in a matrix environment. RESPONSIBILITIES The Clinical Trial Manager (CTM) works closely with various sponsors, internal team members and vendors as well as clinical study sites to ensure that clinical trials are conducted in a timely fashion and in a manner compliant with SOPs, ICH/GCP/regulatory guidelines, study protocol, company goals, and budgets.

30+ days ago

Senior Clinical Operations Lead Sarepta Therapeutics Inc.

Cambridge, MA

$152,400–$190,500 / year

The Senior Clinical Operations Lead, Clinical Operations manages all aspects of assigned clinical trials as well as the study project plan, including timeline, budget, and vendors and is expected to conduct large studies of high complexity. Works cross-functionally to ensure clinical program timelines and goals are met and risks are appropriately escalated to the Clinical Operations Program Lead (COPL).

30+ days ago

Sr. Medical Director, Clinical Sciences Genetix Biotherapeutics Inc

Somerville, MA

$340,000–$350,000 / year

Medical Director, Clinical Sciences, will work closely with the Head of Clinical Sciences, to provide medical leadership and operational oversight for clinical development programs in hemoglobinopathies, specifically working on an ongoing registration-directed trial in children with sickle cell disease (SCD), the initiation of new trial(s) to evaluate a new manufacturing process and treatment of SCD patients with a history of stroke, and improving the efficiency of ongoing registry and long-term follow-up trials. This role will collaborate cross-functionally with Clinical Operations, Regulatory Affairs, Translational Medicine, Medical Affairs and external stakeholders to ensure the successful execution of clinical trials, analysis and reporting of clinical trial data, and advancement of gene therapy programs.

24 days ago

Clinical Research Coordinator New England College of Optometry

Boston, MA

The primary study is PICNIC, a longitudinal study in children that aims to understand the intrinsic mechanisms whereby some children develop myopia. We use a variety of clinical and laboratory research methodologies, including psychophysics, aberrometry, gaze-contingent eye-tracking and biometry.

30+ days ago

Executive Director / Vice President, Medical Affairs Relay Therapeutics, Inc.

Cambridge, MA

$225,000–$353,000 / year

You will lead the Medical Affairs function through this pivotal transition from late-stage development to commercialization readiness, partnering closely with internal and external stakeholders to develop solutions that drive awareness of Relay Therapeutics' genetic vascular anomaly portfolio, incorporate critical insights into medical strategy, and build external networks and partnerships to advance clinical trials, patient identification, and access to specialized care. Built on unparalleled insights into protein motion and how this dynamic behavior relates to protein function, we aim to effectively drug protein targets that have previously been intractable, with an initial focus on enhancing small molecule therapeutic discovery in targeted oncology.

24 days ago

Senior Clinical Trial Manager (Global) Bicara Therapeutics Inc

Boston, MA

FICERA specifically addresses a key challenge in solid tumor treatment by enabling immune cell penetration into tumors, reducing fibrosis and immunosuppression while reversing TGF--driven resistance mechanisms - ultimately designed to drive the deep, durable responses that may translate into better outcomes and survival for patients. Founded in 2020, we've built a global team of over 100 employees headquartered in Boston, with a clear focus on advancing our lead asset, ficerafusp alfa, or FICERA - a potentially first-in-class bifunctional EGFR-directed antibody combined with a TGF- ligand trap.

30+ days ago

Senior Director, Clinical Dosimetry & Radiation Sciences Alpha-9 Oncology, Inc.

Boston, MA

This role operates at the intersection of clinical development, clinical pharmacology, regulatory affairs, and external imaging partners, with direct influence on how quantitative radiopharmaceutical data is translated into clinical decisions. Reporting into Clinical Development, this role serves as the internal scientific lead for dosimetry methodology and imaging quantification, ensuring rigor, consistency, and interpretability across multiple active studies.

30+ days ago

Executive Director, Clinical Development Centessa Pharmaceuticals, LLC

Boston, MA

$300,000–$375,000 / year

Strong knowledge in clinical development strategy, clinical trial design, regulatory pathways, biostatistics methodologies, and ability to analyze and interpret translational medicine, clinical, and research data as it relates to an asset, patients, etc. Lead clinical development contributor to regulatory activities, submissions, and clinical sections of regulatory/health authority pre-meeting packages and initial applications, routine annual reports, ad hoc safety reports (SUSARs), interim and final CSRs, etc.

30+ days ago

Vice President, Head of Government Partnerships Lila Sciences

Cambridge, Massachusetts

Full-time U.S. employees receive a comprehensive benefits program including medical, dental, and vision coverage; employer-paid life and disability insurance; flexible time off with generous company wide holidays; paid parental leave; an educational assistance program; commuter benefits, including bike share memberships for office based employees; and a company subsidized lunch program. Reporting to the Chief Revenue & Product Officer, you will manage a small but growing team, represent Lila at the highest levels of agency and interagency engagement, and serve as a key member of the company's leadership team.

18 days ago

Portfolio Manager, Government Partnerships (DARPA & ARPA-H) Lila Sciences

Cambridge, Massachusetts

A unified external narrative: You will translate Lila's scientific thesis and autonomous-science workflows into compelling federal/international narratives, partnering with communications, policy, and technical teams to maintain one voice across the portfolio — tuned to DARPA's appetite for revolutionary capability bets and ARPA-H's mission-driven biomedical breakthroughs. A trusted agency posture: You will own Lila's relationships across your assigned portfolio of agencies, program offices, and/or international counterparts — starting with DARPA and ARPA-H — building a clear, credible, technically grounded presence reflected in every external interaction.

28 days ago

Manager, Global Regulatory Operations Disc Medicine Inc

Massachusetts, MA

$128,000–$156,000 / year

IMPDs, meeting packages and CSRs), assisting with regulatory submission activities, performing Veeva RIM inputs, interacting with project team members and Regulatory vendors, authoring best practices and providing associated training as assigned, and other Regulatory Operations projects as needed. Prior experience with submission management and pre-publish compilation tasks for various IND submission types and subsequent post-publish eCTD review processes a plus.

30+ days ago

Lead Medical Science Liaison, Molecular Imaging (Northeast) Bayer AG

Boston, MA

$168,500–$252,800 / year

Bayer seeks an incumbent who possesses the following: Required Qualifications: At minimum, a Bachelor's Degree is required; At least 2 years' industry experience is required; Strong presentation, verbal, and communication skills; Excellent oral and written communication skills; Excellent interpersonal skills; Working knowledge of FDA, OIG requirements; Valid Driver's License and eligibility to drive a company car or pooled vehicle (driving record must meet guidelines base on the company's Risk Screening for Hiring Drivers and MVR will be reviewed as part of pre-employment screening). Location:United States: Connecticut: Residence Based || United States: Massachusetts: Boston || United States: Massachusetts: Residence Based || United States: New Jersey: Residence Based || United States: New York: Manhattan || United States: New York: Residence Based || United States: Rhode Island: Residence Based Division:Pharmaceuticals Reference Code:872531 Contact Us Email:hrop_usa@bayer.com.

30+ days ago

Vice President, Head of Medical – Anti-Infective, Respiratory, Gastrointestinal & Other Therapeutic Areas (ARGO) Azurity Pharmaceuticals - US

Woburn, MA

Azurity Pharmaceuticals is seeking a Vice President, Head of Medical – Anti-Infective, Respiratory, Gastrointestinal & Other Therapeutic Areas (ARGO) to provide senior medical and scientific leadership across Azurity's portfolio in global markets . As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline.

30+ days ago

Vice President, Head of Medical - Anti-Infective, Respiratory, Gastrointestinal & Other Therapeutic Areas ARGO Azurity Pharmaceuticals Inc

Woburn, MA

Azurity Pharmaceuticals is seeking a Vice President, Head of Medical - Anti-Infective, Respiratory, Gastrointestinal & Other Therapeutic Areas (ARGO) to provide senior medical and scientific leadership across Azurity's portfolio in global markets. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline.

30+ days ago

Research Nurse (Per Diem) - Massachusetts Syneos Health

Massachusetts

Fully conversant with the trial protocol, Case Report Forms (CRFs/eCRF), off-site manual (if applicable), supporting documents, procedures, and timelines to enable day to day running of the trial including all relevant SOPs. Ensure the accurate reporting of adverse events (AEs) and serious adverse events (SAEs)/suspected unexpected serious adverse reactions (SUSARs) to the site team and relevant RNPM, providing support for any additional follow-up that may be required.

30+ days ago

Medical Director/Sr Director, Clinical Research Scholar Rock Holding Corp

Cambridge, MA

Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. Serve as subject matter expert, leading efforts to provide scientifically robust evaluation of development strategy and plans, including robust literature review to perform disease area assessment, development landscape analysis, and development and regulatory pathway evaluation.

30+ days ago

Resume Resources

Free Resume Templates Free Resume Builder

Get noticed by top employers!

Upload your resume to let employers know you're open to Investigator job opportunities. Plus, receive relevant job recommendations in your inbox.

Create A Free Account

Investigator Jobs in Chestnut Hill, MA

Rapid Intervention & Survival Skills Instructional Assistant Program Coordinator Commonwealth of Massachusetts

Supervising Attorney - PDD Framingham Commonwealth of Massachusetts

Lead Administrative Assistant - Public Defender Division Administration Commonwealth of Massachusetts

Director of Scientific Communications & Evidence Generation Genetix Biotherapeutics Inc

Clinical Trial Manager Prometrika LLC

Senior Clinical Operations Lead Sarepta Therapeutics Inc.

Sr. Medical Director, Clinical Sciences Genetix Biotherapeutics Inc

Clinical Research Coordinator New England College of Optometry

Executive Director / Vice President, Medical Affairs Relay Therapeutics, Inc.

Senior Clinical Trial Manager (Global) Bicara Therapeutics Inc

Senior Director, Clinical Dosimetry & Radiation Sciences Alpha-9 Oncology, Inc.

Executive Director, Clinical Development Centessa Pharmaceuticals, LLC

Vice President, Head of Government Partnerships Lila Sciences

Portfolio Manager, Government Partnerships (DARPA & ARPA-H) Lila Sciences

Manager, Global Regulatory Operations Disc Medicine Inc

Lead Medical Science Liaison, Molecular Imaging (Northeast) Bayer AG

Vice President, Head of Medical – Anti-Infective, Respiratory, Gastrointestinal & Other Therapeutic Areas (ARGO) Azurity Pharmaceuticals - US

Vice President, Head of Medical - Anti-Infective, Respiratory, Gastrointestinal & Other Therapeutic Areas ARGO Azurity Pharmaceuticals Inc

Research Nurse (Per Diem) - Massachusetts Syneos Health

Medical Director/Sr Director, Clinical Research Scholar Rock Holding Corp

Resume Resources

Similar Job Searches