58 Results for

Surveillance Investigator Jobs in Massachusetts

Jobs

Boston, MA

$25–$30 / hour

In this role, you will conduct field surveillance investigations by observing, tracking, and documenting subjects’ activities, capturing detailed video evidence, and preparing comprehensive reports for client review. Traditional Keyboard refers to a panel of keys used as the primary input device on a computer, typographic machine, or 10-Key numeric keypad.

3 days ago

Springfield, MA

$20–$26 / hour

Check out our YouTube channel to learn more about what a day-in-the-life of a surveillance investigator looks like: Frasco, Inc | YouTube Channel . Minimum Auto Insurance Coverage: $100,000 per person, $300,000 per accident bodily injury, and $50,000 property damage.

3 days ago

Boston, Massachusetts

VRC provides their investigators with necessary equipment and comparable pay, to include drive time, above normal commute mileage reimbursement, company paid licensing fees in most states and allowance for non-reimbursed business expenses. We currently have career opportunities for experienced, self-determined, and highly motivated SURVEILLANCE INVESTIGATORS that would like to join our team of professionals in our efforts to deter and combat insurance fraud.

4 days ago

Bridgewater, MA

Part time

Our leadership team brings over 25 years of field experience and is committed to fostering a professional, results-driven environment. Join Lemieux & Associates, a trusted leader in investigative services, and make an impact with your surveillance expertise.

30+ days ago

Salem, MA

The Surveillance Investigator will perform discreet mobile and stationary surveillance of a Claimant to confirm current activities and capabilities to assist with the administration of an insurance claim. RESPONSIBILITIES: Conduct independent investigations of insurance claims across a range of coverage types, including workers' compensation, general liability, property and casualty, and disability.

9 days ago

Boston, Massachusetts

Through our operating brands, HVACi, StrikeCheck, National Fire Experts, Donan Engineering, BSC Forensics, Component Testing Laboratories, The Robison Group, VRC Investigations, TechLoss, Mecanica Scientific Services, and HMI we are respected as the industry leader for our scale and our track record of conducting expert, specialized, and accurate investigations. Individuals selected for the position will be expected to perform investigations of workers compensation claims, liability investigations, multi-line insurance claims, criminal and civil background checks, and other investigative tasks.

4 days ago

Boston, MA

Investigator'',''Investigator'',''United States-Massachusetts-Boston-1 Ashburton Place'',''United States-Massachusetts-Boston-1 Ashburton Place'',''Unclassified'',''Unclassified'',''Office of the Attorney General'',''Office of the Attorney General'',''Full-time'',''Full-time'',''Day'',''Day'',''Jun 30, 2026, 12:17:54 PM'',''Jun 30, 2026, 12:17:54 PM'',''1'',''1'','''','''','''',''Yearly'',''Non- Executive Branch Agency'',''Non- Executive Branch Agency'',''0000000000'','''','''','''','''','''','''',''false'',''1088359'',''1088359'',''true'',''1088359'',''false'',''Submission for the position: INVESTIGATOR I, INVESTIGATOR II, AND INVESTIGATOR III - (Job Number: 260004OV)'',''false'',''1088359'',''false'',''true''. The Investigator will: review complaints against providers; access Medicaid claims and conduct data analysis; research program rules and regulations; develop investigative plans; analyze financial records; review medical records; interview witnesses; conduct surveillance; serve subpoenas; help execute search warrants; draft interview and investigative reports and memos; collect and secure evidence; conduct public records searches; serve as a witness in criminal and civil proceedings; and perform other investigative tasks necessary to root out fraud, waste, and abuse.

4 days ago

Boston, MA

Full time

Our Full-Time Entry-Level Field Investigator position will help launch your career by providing you with an industry leading FULLY PAID Investigator Training Program - no prior experience necessary! Documentation: Finalize case files by submitting case reports and uploading video footage via personal laptop at the end of the day.

30+ days ago

Cambridge, MA

Full time

Previous Experience: Demonstrated proficiency in covert surveillance techniques, capturing high-quality video footage, and preparing thorough, well-organized investigative reports. This role involves performing both stationary and mobile surveillance, obtaining video and photographic evidence, and preparing thorough, detailed reports for clients.

28 days ago

Boston, MA

Part time

30+ days ago

Taunton, MA

$25–$32 / hour
Part time

30+ days ago

Marlborough, MA

The incumbent may be required to perform additional duties related to the functions listed below, as reasonably necessary to meet business needs, including but not limited to: Developing professional expertise, applies company policies and procedures to resolve a variety of issues, including fulfillment, assay and instrument complaints. Driven by our purpose to enable healthier lives everywhere, every day, we are seeking a talented and experienced Electrical Engineer to join a growing R&D department in our Surgical Division to contribute to new .

16 days ago

Worcester, MA

Accident Investigator II'',''United States-Massachusetts-100 Front Street - Worcester'',''United States-Massachusetts-100 Front Street - Worcester'',''Compliance and Certification'',''Compliance and Certification'',''Department of Workforce Development'',''Department of Workforce Development'',''Full-time'',''Full-time'',''Day'',''Day'',''Apr 24, 2026, 4:13:22 PM'',''Apr 24, 2026, 4:13:22 PM'',''1'',''1'',''101,467.86'',''71,613.10'',''101,467.86'',''Yearly'',''Karen Haynes-Clifton'',''Karen Haynes-Clifton'',''6176265138'',''01-NAGE - Clerical/Administrative'',''01-NAGE - Clerical/Administrative'',''No'',''No'',''No'',''No'',''false'',''1082960'',''1082960'',''true'',''1082960'',''false'',''Submission for the position: Ind. Works with outside agencies relating to the claim Conducts internet and social media research on subjects related to claim Interviews all relevant parties to the claim, in person if possible Attends and participates in conciliations, conferences and court proceedings as needed Conducts physical site visits of claim locations and obtain pictures if relevant.

30+ days ago

Dorchester, MA

$96,690–$107,430 / year

Conducts all phases of revenue recovery investigations including the attainment of depositions and supporting data for both judicial and administrative processing as well as fact-finding from Company and Public records related to theft of service cases. Current guidelines require employees to work at least three days in the office, including Tuesdays and Wednesdays, with the third day set by the employee and supervisor based on department needs.

30+ days ago

Taunton, MA

Part time

We're actively seeking retired and former law enforcement professionals to join our Special Investigations Unit (SIU) as Investigators. Join a team where your background is respected, your voice is heard, and your work continues to make a difference.

24 days ago

BEVERLY, MA

Corporate private investigations agency seeks contract Private Investigator to work undercover at a North Shore assignment in warehouse & distribution. Ideal opportunity for Criminal Justice students/graduates and/or individuals seeking investigative experience in pursuit of a career in law enforcement.

30+ days ago

Boston, MA

Driving Positions: must possess a valid Driver's License with at least one year of driving experience, a clean driving record (no major violations within last 36 months, no more than 1 accident in last 24 months, no more than one minor moving violation in last 24 months), a minimum level of insurance as required by Company policy, and the ability to safely operate a vehicle required. Allied Universal SkillBridge Program Allied Universal partners with the U.S. Department of Defense (DoD) SkillBridge Program to support transitioning service members with up to 180 days of on-the-job training during their final months of active duty, while they continue to receive full DoD pay and benefits.

30+ days ago

Waltham, MA

$145,000–$155,000 / year

The Clinical Scientist will be responsible for leading ongoing clinical data review activities, developing data review strategies, identifying and resolving data issues, and ensuring high-quality clinical datasets are available to support safety reviews, regulatory submissions, and clinical decision-making. This unique role sits at the intersection of Clinical Development, Clinical Operations, Data Management, and Biostatistics serving as a critical driver of data quality, data integrity, and clinical insight generation.

3 days ago

North Andover, Massachusetts

$95,000–$105,000

We offer iconic brands such as NeeDoh®, LAVA® Lamp, Big Wheel®, Schylling hand puppets, Sea-Monkeys® and a variety of other toys that satisfy curiosity, encourage discovery, and help people find their best mellow and chill. This role will serve as the central point of contact between Schylling, outside counsel, investigators, online enforcement vendors, and internal teams to help protect the company’s brands, trademarks, copyrights, and products from infringement and counterfeiting.

19 days ago

Boston, MA

As the clinical voice of the physician and patient, the Global Medical Director will partner with Clinical Research, Research and Development (R&D), Quality, Regulatory Affairs and Commercial teams to support innovation, clinical evidence generation, product development and patient safety. Partner with Clinical Research, Clinical Evidence, Quality, Regulatory Affairs, R&D, Marketing and Business Development teams to support product strategy and medical decision-making.

26 days ago

Marlborough, MA

This Engineering Technician role supports post-market surveillance (PMS) laboratory operations within a medical device environment, with responsibilities spanning returned product inspection, complaint processing, preventive maintenance, and continuous improvement initiatives. Technician educational program completed (350 studying hours) or 30% of a bachelor's degree in an engineering career or similar.

12 days ago

Boston, Massachusetts

The framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success. Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission.

10 days ago

Somerville, Massachusetts

Strong time management skills and the ability to work independently across multiple concurrent projects while meeting deadlines; strong written and verbal communication skills, including the ability to document workflows clearly and coordinate with clinical, academic, and public health partners; comfort with data entry and basic data review tools (e.g., Excel) and familiarity with electronic documentation practices. Core activities include specimen receipt and QC, aliquoting and storage, nucleic acid extraction, routine molecular testing, laboratory information management system (LIMS) data entry and reconciliation, chain of custody documentation, and the day to day inventory management of a high volume biorepository.

17 days ago

Boston, MA

$230,000–$317,000 / year

Minimum 8 years of experience as pharmacovigilance physician with strong experience in handling ICSR processing for clinical trials and marketed drugs, signal detection , aggregate reports development and safety analyses from clinical trials. The Medical Safety Physician will be responsible for the medical safety activities of all pharmacovigilance activities for the assigned products including medical review of all ICSR, aggregate reports related activities and support signal detection, risk management, and submission associated activities.

18 days ago

Boston, MA

Develop processes for and provide safety medical oversight of safety surveillance and benefit risk assessments, including medical review of ICSRs, signal management activities, safety analyses, benefit risk profile development and monitoring, and risk mitigation strategies. This role requires a hands-on leader with robust medical and operational expertise, a strong understanding of global regulatory requirements, and the ability to design and oversee a robust fit-for-purpose safety system that scales with company growth to support excellence in Drug Safety & Pharmacovigilance as a critical part of our mission.

4 days ago

Boston, Massachusetts

Full time

This 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.

30+ days ago

Waltham, MA

$145,000–$155,000 / year

The Clinical Scientist will be responsible for leading ongoing clinical data review activities, developing data review strategies, identifying and resolving data issues, and ensuring high-quality clinical datasets are available to support safety reviews, regulatory submissions, and clinical decision-making. Position Summary: TScan is seeking a highly motivated and detail-oriented Clinical Scientist with deep expertise in clinical data management and data review to support the execution of our oncology cell therapy clinical programs.

3 days ago

Waltham, MA

The Safety Scientist collaborates primarily with the Product Safety Lead/Safety Physician for assigned products, and also with cross-functional team members to ensure active safety surveillance of SAEs and other clinical trial safety data and lead/assist in the preparation of safety-related documents. Cross-Functional Collaboration: Work closely with clinical operations, clinical development, regulatory affairs, and other departments, including the PV vendor, to ensure the safety of clinical trial participants.

13 days ago

Waltham, MA

The Senior Safety Scientist collaborates primarily with the Product Safety Lead/Safety Physician for assigned products, and also with cross-functional team members to ensure active safety surveillance of SAEs and other clinical trial safety data and lead/assist in the preparation of safety-related documents. Cross-Functional Collaboration: Work closely with clinical operations, clinical development, regulatory affairs, and other departments, including the PV vendor, to ensure the safety of clinical trial participants.

13 days ago

$103,872–$130,886 / year

This is an opportunity to influence how leading biotechnology, pharmaceutical, research, and high-tech organizations design and run their biosafety and health & safety programs-moving beyond compliance toward resilient, high-performing systems that enable innovation while protecting people and operations. Who We Are: As the largest global pure play sustainability consultancy, we partner with the world's leading organizations, creating innovative solutions to sustainability challenges and unlocking commercial opportunities that meet the needs of today while preserving opportunity for future generations.

30+ days ago

Bedford, MA

$279,000–$332,000 / year

Collaborate with the Head of Pharmacovigilance and PV Operational leadership on PV departmental capability building, PV System building, developing medical strategies, contributing medical expertise to PV procedures, vendor oversight and safety database governance as it relates to medical review processes. Lead medical review of individual case safety reports (ICSR), including serious adverse events (SAE) and adverse events of clinical interest (AECI) across clinical and postmarketing settings; oversee medical review of ICSR performed by vendors/contractors.

30+ days ago

Remote

$126,000–$178,000 / year

As a Manager, Product Quality Clinician, you will be a member of Complaint Handling and Post Market Surveillance/Risk Management team to provide clinical guidance/clinical expert knowledge to Quality, Engineering and other cross functional teams to understand the nature of complaints and possible health risks. How you will make an impact: Provides medical/clinical guidance to complaint investigators and engineers related to event interpretation, event investigation, proper coding, required regulatory reporting (Medical Device Reports, Medical Device Vigilance, etc.), and complaint closure.

17 days ago

Boston, MA

This 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. 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.

30+ days ago

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

Boston, MA

$350,000–$380,000 / year

Centessa Pharmaceuticals plc (Nasdaq: CNTA) new kind of pharmaceutical company with a deconstructed R&D environment that prioritizes data driven decision making led by subject matter experts. The VP will drive an integrated, science-driven global safety strategy for the company's small molecule pipeline, working closely with internal stakeholders and teams, as well as global health authorities.

30+ days ago

$181,400–$326,500 / year

In partnership with Medical Safety leadership, oversee medical safety and risk management for the Vascular portfolio, ensuring compliance with global regulatory requirements (e.g., FDA, PMDA, Notified Bodies, GLPs) and providing clinical expertise for adverse event assessment, post‑market surveillance, risk management planning, safety communications, and Field Action Committee activities. Engage early and continuously with cross‑functional partners, including Marketing, Regulatory, R&D, Clinical Affairs, Quality, Business Development, Scientific Affairs, Physician Training, and Global Medical Affairs Regions to align medical strategy with program and platform objectives.

30+ days ago

Cambridge, MA

$178,500–$297,500 / year

Review, preparation, contribution and/or approval of clinical development documents including clinical development plans, SAPs, study protocols, investigator brochures, data monitoring plans, study reports, integrated summary of safety, summary of clinical safety, and labeling. But progress doesnt happen without people people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen.

30+ days ago

Boston, MA

$288,059.20–$432,088.80 / year

The successful Study and Program Clinical Lead in Late Phase CVRM (Cardiovascular, Renal, and Metabolic diseases) will be responsible for the design, conduct, monitoring, data interpretation and reporting of clinical trials ensuring that the clinical data collected within the study will allow determination of the benefits and risks of the compound, as well as will allow for the intended label indication and price in markets globally. Is accountable for delivery of the clinical components of all relevant study documents (e.g Protocol, Amendments, Statistical Analysis Plan, Informed Consent Form, Case Report Forms, and Safety and Risk-Based Monitoring Plans).

30+ days ago

Cambridge, MA

$210,000–$260,000 / year

Work closely with the Medical/Safety Lead to support signal detection activities, which may include: preparing signal assessment, tracking, and validation documents; leading cross functional teams to assess safety signals; preparing action and communication plans to mitigate/manage product risks; responding to safety related regulatory requests; developing and maintaining product risk management plans. The Director of Pharmacovigilance will contribute to a full range of pharmacovigilance activities including but not limited to the oversight and management of safety reports and safety data, signal management activities, PV organization and process development, inspection readiness, PV vendor management, and operational support for Beam products throughout the lifecycle.

22 days ago

Cambridge, MA

$178,500–$297,500 / year

The role of the DMD is to: Collaborate with other medical and clinical scientific experts DMDs or Development Scientific Directors (DSDs) in the project under the leadership of the Global Project Head, with the Global safety Officer, Regulatory Strategist and other key functional representatives to deliver development strategy and prepare/assist with regulatory bodies interaction. Provide appropriate clinical scientific input & support for all activities related to clinical studies conduct such as answers to IRBs and HA questions, protocol scientific and medical training, medical review of data within the scope of the Centralized monitoring, clinical and medical information for the study team, medical advisors/Clinical Project Leaders from Clinical Study Units, and investigators.

30+ days ago

NEWVEC invites applications for a Postdoctoral Research Fellow to lead a newly funded project focused on developing operational, evidence-based tools and strategies to reduce the incidence of human-biting ticks on coastal island community. The New England Center of Excellence in Vector-borne Diseases (NEWVEC) is a multi-institutional, federally supported research and training center dedicated to reducing the burden of vector-borne diseases across the New England region and beyond.

30+ days ago

Boston, MA

$288,059–$432,088 / year

Scientific and medical responsibilities include: • Study design concept delivery • Driving clinical and scientific decisions within Global Study Team • Accountable for clinical, scientific, and ethical components of studies including patient safety on a study and/or program level in compliance with Good Clinical Practice • Accountable for scientific medical input to all study documents to ensure consistency within clinical program and alignment with scientific rationale. Regulatory interactions: • Plays key role in development of the clinical sections of regulatory submission documents • Provides leadership in writing responses to comments/questions of Regulatory Authorities for clinical modules • Leads the strategy for the development of regulatory agency briefing documents and ensure completeness; may also defend positions during regulatory meetings.

30+ days ago

Waltham, MA

Oversees analysis of aggregate safety data and the production of key company documents such as DSURs (Development Safety Update Reports), PSURs (Periodic Safety Update Reports) and risk management plans relating to the safety of medicinal products, which are subject to regulatory review and discussion. 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.

30+ days ago

Cambridge, MA

$210,000–$260,000 / year

19 days ago

Massachusetts

Experience applying AI, machine learning, or advanced analytics in clinical development or research (e.g., protocol design and optimization, site selection and feasibility assessment, query management and workflow automation, data cleaning, anomaly detection, and signal identification, safety risk prediction and proactive mitigation). Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.

30+ days ago

Lexington, Massachusetts

The successful candidate will act as a primary bridge between raw clinical data and clinical decision-making, working in close collaboration with the Chief Medical Officer, Clinical Development Lead, and cross-functional program team. Data Integrity & Resolution: Identify missing data points or clinical anomalies and proactively coordinate with internal teams and clinical sites to ensure timely resolution and data accuracy.

13 days ago

Waltham, Massachusetts

Physical demands are those in excess for sedentary work; must be able to remain on feet for extended periods of time, stoop, kneel, crouch, lift, carry, push, pull, climb stairs, balance, walk, and run; must be able to access all facilities on foot; must be able to conduct visual surveillance of individuals and surroundings; must be physically able to operate and communicate using a variety of machines and equipment including baton, automobile, office equipment, radio, telephone, etc; work includes considerable exposure to unusual elements, such as severe weather/ temperatures and loud noises; work environment involves moderate exposure to hazards and physical risks to personal safety. The Sergeant manages and supervises the campus police, security staff, and parking monitors, providing 24/7 coverage for the department, to help accomplish the department’s overall mission to provide a safe and secure environment all faculty, staff, students, and visitors/guests to the university and to protect life and property on and around the Brandeis campus.

3 days ago

Raynham, MA

$199,000–$343,275 / year

Assist medical evidence generation leaders to develop and execute global strategies for evidence generation for new and existing products, including medical interpretation of clinical analyses, and in the review and approval of clinical study reports and scientific articles (abstracts, manuscripts, etc), in order to support regulatory approval/clearance, health technology assessment, customer access, medical safety and post-marketing support. Support business leaders by providing medical and scientific expertise and omni-channel insights to help shape optimal business development strategy and targets, including product launches, key scientific meetings, relationship management with leading research physicians, critical evaluation of current literature and competitive activity, and in other domains where medical and scientific expertise is required.

30+ days ago

Waltham, MA

$245,000–$300,000 / year

The Senior Director partners closely with Global Medical Directors, HEOR, Clinical Development, Biometrics, Drug Safety/Pharmacovigilance, Regulatory Affairs, Value & Access, and Commercial to generate and interpret evidence that enables asset‑level Medical Affairs strategies. Leads the design, execution, and interpretation of epidemiologic and observational studies supporting Medical Affairs objectives, including chart reviews, post hoc analyses, prospective observational studies, investigator-initiated studies, Phase 3b/4 studies, and prevalence/incidence studies.

27 days ago

Warren, Massachusetts

This Director position is directly responsible for all aspects of Global Patient Safety activities for assigned compounds and products in support of safety surveillance, signal management, communication of the safety profile as appropriate for the stage in the asset lifecycle, benefit risk assessment, safety responses to regulatory agency queries, safety documents (DSURs, PSURs, development RMPs, RMPs, etc.) and the review of clinical documents (Investigator Brochures, protocols, clinical study reports, etc.). Represent Global Patient Safety for assigned compounds on cross-functional teams, including Regeneron’s Safety Oversight Committee (RSOC), Independent Data Monitoring Committees (IDMC), Strategic Program Team (SPT) and other teams with members external to Regeneron (alliance partners, CROs).

27 days ago

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Surveillance Investigator Jobs in Massachusetts

Surveillance Investigator II Command Investigations, LLC

Surveillance Investigator Frasco Inc

Surveillance Investigator VRC Investigations

Surveillance Investigator Lemieux & Associates LLC

Surveillance Investigator Allied Universal

Part-time Surveillance Investigator The Robison Group

INVESTIGATOR I, INVESTIGATOR II, AND INVESTIGATOR III Commonwealth of Massachusetts

Entry-Level Investigator Ethos Risk Services

Investigator Ethos Risk Services

Surveillane Investigator Lemieux & Associates LLC

SIU Claims Investigator - Spanish Speaker Lemieux & Associates LLC

Post Market Surveillance Specialist Hologic Inc

Ind. Accident Investigator II Commonwealth of Massachusetts

Revenue Assurance Investigator (Hybrid) Eversource

Private Investigator - Retired/Former Law Enforcement Lemieux & Associates LLC

Undercover Investigator DATA QUEST INVESTIGATIONS LTD

Security Shift Supervisor Pharma Allied Universal

Clinical Scientist TScan Therapeutics

Intellectual Property & Legal Coordination Manager Schylling

Medical Director, EP, Medical and Patient Safety Gateway Recruiting

Engineering Technician GTT, LLC

Veterinary Technician, MGH Center for Comparative Medicine Mass General Brigham

BFT - Research I Mass General Brigham

Medical Safety Physician, Pharmacovigilance Verastem Inc

Vice President, Global Head of Drug Safety (DS) & Pharmacovigilance (PV) Hemab ApS

Director, Drug Safety & Pharmacovigilance (Inflammation & Oncology) Monte Rosa Therapeutics, Inc

Clinical Scientist TScan Therapeutics Inc

Safety Scientist Viridian Therapeutics Inc

Senior Safety Scientist Viridian Therapeutics Inc

Managing Consultant, Health & Safety (Biosafety Focus) ERM International Group Ltd

Medical Director, Pharmacovigilance Stoke Therapeutics Inc

Manager, Product Quality Clinician - Medical Device / Complaint Handling & Cardiovascular RN Edwards Lifesciences Corp

Director, Drug Safety & Pharmacovigilance (Inflammation & Oncology) Monte Rosa Therapeutics Inc

Executive Director, Clinical Development Centessa Pharmaceuticals Plc

Vice President, Pharmacovigilance & Safety Centessa Pharmaceuticals Plc

Senior Director, Medical Affairs, BDPI - Vascular Platform Becton Dickinson and Co

Global Safety Officer, I&I Sanofi

Senior Director, Global Clinical Program Lead AstraZeneca Plc

Director, Pharmacovigilance Beam Therapeutics Inc

Development Medical Director - Clinical Research Director Sanofi

Post Doctoral Research Associate - New England Center of Excellence in Vector-borne Diseases (NEWVEC) University of Massachusetts Amherst

Global Clinical Program Lead AstraZeneca Plc

Global Safety Lead - Formulation Safety CSL Behring LLC

Director, Pharmacovigilance Beam Therapeutics

Clinical Development Scientist, Director (Inflammation and Immunology) Pfizer

Associate Director, Clinical Scientist Kiniksa Pharmaceuticals

Sergeant - Public Safety Brandeis University

Medical Director Orthopaedics, Spine Johnson & Johnson

Senior Director, Epidemiology and Real World Evidence Dyne Therapeutics Inc

Director, Global Patient Safety Sciences - General Medicine Regeneron Pharmaceuticals

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