Top 196 Regulatory affairs lead Jobs in Princeton Nj

Senior Director, Clinical Safety Scientist
Daiichi Sankyo, Inc. —Basking Ridge, NJ
- $242,700 - $404,500 a year
- 5 years
- Doctor of Philosophy
- Mentoring
Senior Director, HEOR and Pricing
Rocket Pharmaceuticals —Cranbury, NJ
- $236,000 - $354,000 a year
- Full-time
- Medicine
- 11+ years
- Analysis skills
- Paid holidays
- Health insurance
6d
Head of Medical Affairs, International Markets - Genmab
Genmab —Princeton, NJ
- $253,440 - $380,160 a year
- Online Application
- Hybrid work
- Medicine
- Management
- 11+ years
- Commuter assistance
- Paid parental leave
Medical Director
Genmab —Princeton, NJ
- $261,120 - $391,680 a year
- Online Application
- Medicine
- 3 years
- Team management
- Commuter assistance
- Paid parental leave
6d
Director, Strategic Clinical Vendor Oversight and Relationship Lead (CRO)
Genmab —Princeton, NJ
- $193,280 - $289,920 a year
- Online Application
- 8 years
- Bachelor's degree
- Training & development
- Commuter assistance
- Paid parental leave
VP, Global Program Lead - Cell Therapy
BMS —Princeton, NJ
- $341,360 - $413,648 a year
- Email
- Hybrid work
- Bachelor of Science
- Office
- Bachelor's degree
- Paid holidays
- Disability insurance
Director to VP of Business Development, Biologic/Biosimilar Products
Prinston Pharmaceutical Inc. —Somerset, NJ
- $200,000 - $250,000 a year
- 8 hour shift
- Marketing
- Office
- Master's degree
- Health insurance
- Dental insurance
Quick Apply
Senior Director Quant Pharm
Penfield Search Partners —Princeton, NJ
- $1 - $2 an hour
- Full-time
- 5 years
- Writing skills
- Doctor of Philosophy
Quick Apply
Chief Product Officer
Grüns —New Brunswick, NJ
- $350,000 a year
- Remote
- 11+ years
- Senior level
- Leadership
- Paid time off
Quick Apply
9d
Corporate Communications Manager
Integra LifeSciences —Princeton, NJ
- $109,250 - $149,500 a year
- Email
- Microsoft Word
- Microsoft Excel
- Marketing
- Disability insurance
- Health insurance
Manager, Regulatory Affairs - Cosmetics (Global)
Church & Dwight —Princeton, NJ
- $110,900 - $157,900 a year
- Full-time
- Remote
- 8 years
- Bachelor's degree
- Continuous improvement
- Profit sharing
- Paid parental leave
Head, Business Operations and Alliance Management
Legend Biotech US —Bridgewater, NJ
- $256,073 - $336,097 a year
- Full-time
- Office
- US work authorization
- Budgeting
Quick Apply
9d
Associate Director, Regulatory Affairs - Biosimilars (US)
Sandoz —Princeton, NJ
- $145,600 - $279,400 a year
- Full-time
- Hybrid work
- 7 years
- Office
- Analysis skills
- Health insurance
- Dental insurance
Director, Regulatory Affairs - Development Strategy
Insmed Incorporated —Bridgewater, NJ
- $185,000 - $252,500 a year
- Full-time
- Remote
- 5 years
- Business development
- Bachelor's degree
- Employee stock purchase plan
- Disability insurance
13d
Regulatory Affairs Project Manager (173814)
Colgate-Palmolive —Piscataway, NJ
- $124,000 - $174,000 a year
- Hybrid work
- Master's degree
- Bachelor's degree
- Travel
- Profit sharing
- Paid parental leave
Manager, Regulatory Affairs - Tactical Implementation
Insmed Incorporated —Bridgewater, NJ
- $133,000 - $173,000 a year
- Full-time
- Remote
- Microsoft Outlook
- 5 years
- Bachelor's degree
- Employee stock purchase plan
- Disability insurance
6d
Senior Director, Regulatory Affairs, Global Regulatory Lead - Development Strategy
Insmed Incorporated —Bridgewater, NJ
- $222,000 - $303,000 a year
- Full-time
- Remote
- 8 years
- Bachelor's degree
- Doctor of Philosophy
- Employee stock purchase plan
- Disability insurance
1d
Associate Media Relations and Issues Management Director
Novo Nordisk —Plainsboro, NJ
- $153,000 - $267,000 a year
- Sales
- Office
- Bachelor's degree
- Disability insurance
- Health insurance
Regulatory Affairs Specialist
Amneal Pharmaceuticals —Piscataway, NJ
- $117,000 - $120,000 a year
- Full-time
- 5 years
- Mid-level
- Office
5d
Vice President, International Markets
Genmab —Princeton, NJ
- $280,000 - $420,000 a year
- Online Application
- 11+ years
- Bachelor's degree
- Senior level
- Commuter assistance
- Paid parental leave

I want to receive the latest job alert for regulatory affairs lead in princeton nj

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

regulatory affairs lead jobs near princeton nj

Communications Manager jobs in Princeton, NJ

Quantitative Analyst jobs in Princeton, NJ

Regulatory Affairs Specialist jobs in Piscataway, NJ

Vendor Manager jobs in Princeton, NJ

Regulatory Affairs Specialist jobs in Bridgewater, NJ

Medical Director jobs in Princeton, NJ

Director Of Regulatory Affairs jobs in Princeton, NJ

Vice President jobs in Princeton, NJ

Regulatory Affairs Specialist jobs in Princeton, NJ

Communications Manager jobs in Virginia

Communications Manager jobs in Wisconsin

Communications Manager jobs in Dallas, TX

Communications Manager jobs in Raleigh, NC

Hotel Manager jobs in Huntsville, AL

Entry Level Health Communications jobs in New York, NY

Remote Case Manager jobs in Florida

Program Manager Healthcare jobs in Chicago, IL

Project Manager jobs in Corpus Christi, TX

Veterans Affairs jobs in Hampton, VA

Regulatory Affairs Manager jobs in Miami, FL

Senior Director, Clinical Safety Scientist

Daiichi Sankyo, Inc. -
Basking Ridge, NJ

Apply Now

Job Details

$242,700 - $404,500 a year

Qualifications

Pharmacovigilance research
Pharmaceutical company experience

Full Job Description

Job Title:
Senior Director, Clinical Safety Scientist

Job Requisition ID:
1430

Posting Start Date:
4/28/26

At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society.

Job Summary

The Senior Director, Clinical Safety Science is a key leadership role responsible for shaping and advancing global safety strategy across the product lifecycle—from early development through post-marketing. This position oversees a team of Safety Scientists who partner with Safety Physicians and cross-functional stakeholders to ensure proactive safety surveillance, benefit-risk assessment, and risk mitigation planning for a group of assets. The Senior Director plays a pivotal role in influencing safety governance, driving innovation in safety science, and ensuring regulatory and compliance excellence. In addition to operational oversight, this role contributes to the development of global safety processes, talent capability building, and strategic alignment across the broader Clinical Safety and Pharmacovigilance (CSPV) function and the enterprise.

Responsibilities

Strategic Safety Leadership: Provide scientific and strategic leadership for safety surveillance and risk management for a group of assets. Lead scientist team to collaborate with safety physicians, regulatory affairs, clinical development, other functions and external partners to deliver high-quality safety assessments, regulatory submissions, aggregate reports, and responses to health authority queries.

Team and Talent Development: Lead, mentor, and develop a high-performing team of safety scientists supporting a group of assets. Champion a culture of scientific rigor, continuous learning, and collaboration. Ensure strategic alignment of talent to pipeline priorities, provide performance feedback, and guide professional growth to build future leadership.

Innovation and Process Excellence: Maintain strong knowledge of the evolving safety science and regulatory landscape. Drive initiatives to enhance scientific methods, tools, and systems supporting safety surveillance and signal detection. Lead cross-functional and global projects to evolve safety science capabilities. Contribute to strategic planning and operating model design for CSPV.

Compliance and Quality Oversight: Ensure all safety deliverables by the scientist team meet internal quality standards and are compliant with GCP/GVP and relevant global regulations. Support audits and inspections, contribute to CAPA development, and foster a culture of quality and accountability.

Resource Planning: Partner with CSPV portfolio management and product leads to forecast resource needs for a group of assets and align capacity with business priorities. Leverage metrics to inform decision-making and improve operational efficiency.

Qualifications

Education Qualifications

PharmD or PhD degree in relevant discipline required

Experience Qualifications

At least 10 years of experience in clinical development, medical affairs or clinical safety/post marketing safety in the pharmaceutical industry required

At least 5 years of experience in clinical safety/post marketing safety in the pharmaceutical industry preferred

At least 5 years of people management experience required

Experience in leading safety scientist teams in clinical studies, regulatory submissions, aggregate reports and post-marketing surveillance and risk management

Excellent communication, project management, writing and analytic skills

Demonstrated strong organizational leadership skills

Extensive knowledge of the latest technical and regulatory development

Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.

Salary Range:
USD$242,700.00 - USD$404,500.00

Download Our Benefits Summary PDF

Professionals

Apply Now

Refine Your Search

regulatory affairs lead jobs in princeton nj

Senior Director, Clinical Safety Scientist

Senior Director, HEOR and Pricing

Head of Medical Affairs, International Markets - Genmab

Medical Director

Director, Strategic Clinical Vendor Oversight and Relationship Lead (CRO)

VP, Global Program Lead - Cell Therapy

Director to VP of Business Development, Biologic/Biosimilar Products

Senior Director Quant Pharm

Chief Product Officer

Corporate Communications Manager

Manager, Regulatory Affairs - Cosmetics (Global)

Head, Business Operations and Alliance Management

Associate Director, Regulatory Affairs - Biosimilars (US)

Director, Regulatory Affairs - Development Strategy

Regulatory Affairs Project Manager (173814)

Manager, Regulatory Affairs - Tactical Implementation

Senior Director, Regulatory Affairs, Global Regulatory Lead - Development Strategy

Associate Media Relations and Issues Management Director

Regulatory Affairs Specialist

Vice President, International Markets

I want to receive the latest job alert for regulatory affairs lead in princeton nj

Related Searches

Explore jobs in more locations

Job Seeker Tools

Employer Tools

Browse

Stay Connected