Top 979 Senior associate director Jobs in Boston Ma

Senior Director, Drug Safety & Pharmacovigilance – Development
Klein Hersh International —Boston, MA
- Email
- Medicine
- 5 years
- Contracts
Associate Director of Operations
Tenacity —Allston, MA
- $65,000 - $75,000 a year
- Full-time
- Hybrid work
- Microsoft Word
- Background check
- Microsoft Excel
- Health insurance
- Dental insurance
Quick Apply
Associate Director, Global Regulatory Affairs - Ad / Promo
BioNTech AG —Cambridge, MA
- $166,000 - $203,000 a year
- Full-time
- Background check
- Bachelor of Science
- 8 years
Associate Director, Clinical Quality Assurance
BioNTech AG —Cambridge, MA
- $163,000 - $200,000 a year
- Full-time
- Background check
- 5 years
- Mentoring
- Health savings account
- AD&D insurance
Senior Living Director of Sales and Marketing
Arbors at Stoneham —Stoneham, MA
- Weekends as needed
- Marketing
- Residential
- Business development experience
Quick Apply
Senior Director / Director Clinical Development, Oncology
BioNTech AG —Cambridge, MA
- $168,100 - $318,300 a year
- Full-time
- Background check
- Medicine
- Mentoring
Associate Director of Business Development - Northeast US (Biotech Services)
Coriolis Pharma Research GmbH —Boston, MA
- Up to 50% travel
- Customer service
- 5 years
Quick Apply
5d
Associate Director of Business Development - Southern West Coast (Biotech Services)
Coriolis Pharma Research GmbH —Boston, MA
- Up to 50% travel
- Customer service
- 5 years
Quick Apply
7d
AIRx, Sr. Director, Nonclinical Safety Lead
Takeda Pharmaceutical —Boston, MA
- $212,000 - $333,190 a year
- Call employer
- Hybrid work
- 11+ years
- Business development experience
- Doctor of Philosophy
- Paid holidays
- Disability insurance
Senior Director of Premium Services - Fenway Park
Aramark —Boston, MA
- $140,000 - $145,000 a year
- 5 years
- Bachelor's degree
- Mentoring
- Disability insurance
- Health insurance
5d
Associate Director, Clinical Assay Strategy, Flu
CSL Seqirus —Waltham, MA
- $179,000 - $212,000 a year
- Full-time
- Hybrid work
- Office
- Bachelor's degree
- Doctor of Philosophy
HFUE Associate Director
Sanofi EU —Cambridge, MA
- $148,500 - $214,500 a year
- Engineering
- English
- Travel
- Parental leave
Senior Director, AIRx Biologics Discovery Lead
Takeda Pharmaceutical —Boston, MA
- $212,000 - $333,190 a year
- Full-time
- Hybrid work
- Laboratory experience
- 11+ years
- Doctor of Philosophy
- Paid holidays
- Disability insurance
Senior Director, AIRx Computational Chemistry
Takeda Pharmaceutical —Boston, MA
- $212,000 - $333,190 a year
- Full-time
- Hybrid work
- 11+ years
- Doctor of Philosophy
- Senior level
- Paid holidays
- Disability insurance
Senior Director and Regulatory Platform Lead GRA CMC, Device and Drug-Device Combinations Human Factors
Takeda Pharmaceutical —Boston, MA
- $212,000 - $333,190 a year
- Full-time
- Hybrid work
- Bachelor of Science
- Business development experience
- Travel
- Paid holidays
- Disability insurance
Research Senior Scientific Director, Head of Hit ID and Sample Management (Automation)
Takeda Pharmaceutical —Boston, MA
- $212,000 - $333,190 a year
- Hybrid work
- Bachelor of Science
- 11+ years
- Presentation skills
- Paid holidays
- Disability insurance
Sales Director Senior Living
Benchmark Senior Living —Danvers, MA
- $79,000 a year
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Research
- Disability insurance
- Health insurance
Quick Apply
Associate Director of Nursing
Lifeworks, Inc. —Westwood, MA
- $112,428.16 a year
- Full-time
- Background check
- RN License
- 3 years
- 403(b) matching
- Disability insurance
Quick Apply
Senior Director, US Rare Disease Value and Access
Sanofi EU —Cambridge, MA
- $206,250.00 - $297,916.66 a year
- 7 years
- Office
- Bachelor's degree
- Parental leave
2d
Senior Director, Immunology and Translation
CSL Behring —Waltham, MA
- $302,000 - $350,000 a year
- Full-time
- Hybrid work
- Medicine
- 11+ years
- Office

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Senior Director, Drug Safety & Pharmacovigilance – Development

Klein Hersh International -
Boston, MA

Apply Now

Job Details

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
Pharmaceutical company experience
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 associate director jobs in boston ma

Senior Director, Drug Safety & Pharmacovigilance – Development

Associate Director of Operations

Associate Director, Global Regulatory Affairs - Ad / Promo

Associate Director, Clinical Quality Assurance

Senior Living Director of Sales and Marketing

Senior Director / Director Clinical Development, Oncology

Associate Director of Business Development - Northeast US (Biotech Services)

Associate Director of Business Development - Southern West Coast (Biotech Services)

AIRx, Sr. Director, Nonclinical Safety Lead

Senior Director of Premium Services - Fenway Park

Associate Director, Clinical Assay Strategy, Flu

HFUE Associate Director

Senior Director, AIRx Biologics Discovery Lead

Senior Director, AIRx Computational Chemistry

Senior Director and Regulatory Platform Lead GRA CMC, Device and Drug-Device Combinations Human Factors

Research Senior Scientific Director, Head of Hit ID and Sample Management (Automation)

Sales Director Senior Living

Associate Director of Nursing

Senior Director, US Rare Disease Value and Access

Senior Director, Immunology and Translation

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