Top 139 Senior forensic investigator Jobs in Boston, Ma

Senior Director, Drug Safety & Pharmacovigilance – Development
Klein Hersh International —Boston, MA
- Email
- Medicine
- 5 years
- Contracts
12d
MSL/Sr Medical Science Liaison - Hematology, Northeast
Genmab —Boston, MA
- $162,320 - $243,480 a year
- Online Application
- Medicine
- Up to 50% travel
- HIPAA
- Commuter assistance
- Paid parental leave
Senior Manager, Clinical Study Quality Lead (Hybrid)
Vertex Pharmaceuticals —Boston, MA
- $137,800 - $206,800 a year
- Full-time
- Hybrid work
- 6 years
- Project management
- Bachelor's degree
- Loan repayment program
- Dental insurance
Senior Financial Investigator
Contact Government Services, LLC —Boston, MA
- $74,156.16 - $107,114.45 a year
- Full-time
- Hybrid work
- Mid-level
- Driver's License
- Presentation skills
- Health insurance
- Dental insurance
Quick Apply
Senior Investigator Digital Forensics, Incident Response (DFIR)
Accenture —Boston, MA
- $59,100 - $205,800 a year
- Full-time
- Hybrid work
- Azure
- Windows
- 3 years
- Paid holidays
- Disability insurance
Senior Clinical Sciences Trial Leader (Multiple Openings)
Novartis —Cambridge, MA
- $126,000 - $234,000 a year
- Full-time
- Hybrid work
- 6 years
- Bachelor's degree
- Doctor of Philosophy
- Health insurance
- 401(k) matching
7d
Senior Director, Search & Evaluation Late TA Lead, Immunology
CSL —Waltham, MA
- $263,000 - $328,000 a year
- Full-time
- Hybrid work
- Medicine
- 11+ years
- Office
Senior Director, Immunology and Translation
CSL Behring —Waltham, MA
- $302,000 - $350,000 a year
- Full-time
- Hybrid work
- Medicine
- 11+ years
- Office
Senior Industrial Security Representative/Facility Security Officer
Leidos —Concord, MA
- $82,550 - $149,225 a year
- Full-time
- Microsoft Excel
- 6 years
- Microsoft Outlook
Research Scientist/Senior Scientist
Silent Spring Institute —Newton, MA
- $105,000 - $225,700 a year
- Email
- US work authorization
- Senior level
- Health insurance
- Dental insurance
Senior Clinical Research Associate - US
Optimapharm d.o.o. —Boston, MA
- $100,000 - $130,000 a year
- Full-time
- Remote
- Nursing
- 5 years
- Computer literacy
- Dental insurance
- Paid time off
12d
Senior Grants Administrator- Pre-Award Administration- Remote Opportunity
Northeastern University —Boston, MA
- $67,855 - $95,845 a year
- Full-time
- Remote
- Customer service
- Mid-level
- Master's degree
- Health insurance
- Dental insurance
Senior Manager/AD, GCP & GVP, QA
Agios Pharmaceuticals —Cambridge, MA
- $131,035 - $230,312 a year
- Remote
- Project management
- Travel
- Senior level
- Health insurance
Senior Clinical Lead, Early Clinical & Experimental Therapeutics
Sanofi —Cambridge, MA
- $236,250 - $393,750 a year
- Hybrid work
- Medicine
- English
- 3 years
- Parental leave
Senior Scientific Director, Oncology Clinical Development (Non-Hodgkin Lymphoma)
AbbVie —Waltham, MA
- $206,500 - $393,000 a year
- Full-time
- Hybrid work
- English
- 8 years
- Business development experience
- Paid holidays
- Health insurance
14d
Medical Science Liaison / Senior Medical Science Liaison - COVID/Virology - New England
Shionogi Inc. —Boston, MA
- $175,000 - $220,000 a year
- Email
- Microsoft Word
- Background check
- Clean driving record
- Health insurance
14d
Senior Program Manager (SPM) - Mastocytosis
Sanofi —Cambridge, MA
- $122,250.00 - $176,583.33 a year
- Microsoft Excel
- Microsoft Outlook
- 5 years
- Health insurance
- Parental leave
7d
Senior Research Administrator
MIT —Cambridge, MA
- Part-time
- Customer service
- Mid-level
- Analysis skills
Senior Specialist, Regulatory Operations
Care Access —Boston, MA
- $90,000 - $100,000 a year
- Full-time
- Remote
- Microsoft Word
- Pass drug screening
- Bachelor's degree
- Health savings account
- Paid holidays
7d
Senior Clinical Scientist
Sanofi —Cambridge, MA
- $148,500 - $214,500 a year
- Master's degree
- Doctor of Philosophy
- Senior level
- Parental leave

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senior forensic investigator jobs near boston, ma

Senior Director, Drug Safety & Pharmacovigilance – Development

Klein Hersh International -
Boston, MA

Apply Now

Job Details

12 days ago

Qualifications

FDA submissions
Managerial strategic planning
Pharmacovigilance research
Adverse event reporting
Clinical trial risk management
Safety regulations
Lean
Investigational new drug (IND) applications
Supplier relationship improvement
ICH guidelines
Vendor compliance management
Vendor relationship management
Contracts
Vendor contract management
Regulatory submission editing and review
Communication with regulatory authorities for clinical trials
Clinical quality assurance standards
Project contract management
Oncology
Clinical program risk management
Cross-functional team management
Cross-functional communication
Senior leadership

Full Job Description

Contact: Kevin Mednick
Phone: (215) 658-1379

Position Overview

Our client is a clinical-stage oncology company focused on expanding the breakthrough potential of targeted radiopharmaceuticals to large patient populations, including those not addressed by existing platform technologies.

This role will serve as the safety expert across programs and drive safety excellence with the clinical development organization. In collaboration with internal and external partners, you will design and implement best-in-class safety practices to ensure global compliance, support health authority submissions, and protect patient well-being and safety.

Key Responsibilities:

Clinical Safety Leadership

Act as the drug safety lead for one or more clinical-stage assets, providing clinical oversight and proactive safety surveillance in collaboration with global program/clinical teams.
Design, direct and conduct ongoing safety surveillance of company drug products using internal and external resources (e.g. CROs/vendors) to ensure delivery of high-quality Drug Safety services, including oversight of patient safety in all ongoing clinical trials. This includes the medical review of (AEs) and Serious AEs (SAEs).
Provide strategic planning, implementation, and management of Drug Safety activities to support the clinical development of company products.
Serve as the clinical safety expert for all assigned products at all stages of clinical development. As needed, provide hands-on oversight of all clinical safety services including review of medical coding of AEs, concomitant medications, and processing of SAEs (review, query generation and resolution, and preparation of case narratives) through the entire lifecycle.
Establish and conduct signal management procedures including signal evaluation reports and recommendations for risk characterization.
Lead the Risk Management Team (RMT) meetings for review of safety data and AE profile, including production of any associated materials (e.g., aggregate reports, charter).
Provide medical review of AE reports to ensure the accuracy, integrity and completeness of information entered in the safety database.
Contribute critical medical input to clinical documents, including protocols, investigator brochures, and informed consents.
Review and approve safety data for regulatory submissions, aggregate safety reports (e.g., DSURs, PSURs/PBRERs, RMPs), and safety sections of CTD documents.
Provide medical expert safety review input for critical documents for clinical development of products (e.g., protocols and amendments, ICFs, IBs, IMPDs, clinical research reports, INDs, CTAs)

Function Building & Operational Oversight

Build and own the internal Drug Safety & PV function with a focus on scalability, agility, and regulatory excellence.
Oversee day-to-day Safety Operations via a partially outsourced model; manage and optimize PV vendor relationships.
Ensure the quality and timeliness of AE processing, safety database management, MedDRA coding, and global reporting.
Develop and maintain PV policies, SOPs, safety governance frameworks, and inspection readiness plans.

Strategic Collaboration & Influence

Serve as a key clinical safety representative on Clinical Study Teams and global program teams (as needed).
Partner closely with Clinical Development, Regulatory Affairs, Quality, and DMPK to align on safety strategies and data interpretations.
Support safety-related interactions with global health authorities, including preparation for and participation in regulatory meetings, inspections or audits.
Bring a solutions-oriented mindset to evolving internal processes and organizational needs as the company scales.

Key Requirements:

MD or equivalent medical degree required; specialty training in oncology.
Strong desire to be part of a mission‐oriented company leading transformative change for patients.
Proven demonstration of transparent communication and fostering open and diverse debate.
Ability to work with agility and manage ambiguity.
Personifies positive energy and exemplifies respect.
Outstanding interpersonal and communication skills, with the ability to foster trust, influence stakeholders, and operate cross-functionally.
A blend of strategic acumen and operational know-how, able to pivot between high-level planning and detailed execution.
5-7+ years of biopharmaceutical industry experience in pharmacovigilance and clinical safety, with demonstrated success in a leadership capacity.
Proven experience managing pharmaco-vigilance in a partially or fully outsourced model, including vendor oversight and contract management.
Expert knowledge of FDA safety regulations, ICH Guidelines, and other applicable regulatory guidance documents; expertise in global safety regulations.
Expertise in clinical safety assessments, safety signal detection and risk management, including interactions with regulatory authorities
In-depth knowledge of global PV regulations and good pharmacovigilance practice requirements, with direct experience in INDs, NDAs/BLAs/MAAs, and other regulatory submissions.
A track record of building or scaling safety functions, especially in lean, high-growth environments.

Location: Boston/RTL/Remote

Location(S)

Boston, MA

If interested, please send a MS Word version of your resume to [email protected]

Apply Now

Refine Your Search

senior forensic investigator jobs in boston, ma

Senior Director, Drug Safety & Pharmacovigilance – Development

MSL/Sr Medical Science Liaison - Hematology, Northeast

Senior Manager, Clinical Study Quality Lead (Hybrid)

Senior Financial Investigator

Senior Investigator Digital Forensics, Incident Response (DFIR)

Senior Clinical Sciences Trial Leader (Multiple Openings)

Senior Director, Search & Evaluation Late TA Lead, Immunology

Senior Director, Immunology and Translation

Senior Industrial Security Representative/Facility Security Officer

Research Scientist/Senior Scientist

Senior Clinical Research Associate - US

Senior Grants Administrator- Pre-Award Administration- Remote Opportunity

Senior Manager/AD, GCP & GVP, QA

Senior Clinical Lead, Early Clinical & Experimental Therapeutics

Senior Scientific Director, Oncology Clinical Development (Non-Hodgkin Lymphoma)

Medical Science Liaison / Senior Medical Science Liaison - COVID/Virology - New England

Senior Program Manager (SPM) - Mastocytosis

Senior Research Administrator

Senior Specialist, Regulatory Operations

Senior Clinical Scientist

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