Top 34 Global safety officer pharmacovigilance Jobs

Global Safety Officer
Sanofi —Cambridge, MA
- $178,500 - $297,500 a year
- Medicine
- BC/BE
- English
- Parental leave
Global Safety Officer, I&I
Sanofi —Cambridge, MA
- $178,500 - $297,500 a year
- Medicine
- BC/BE
- English
- Parental leave
Global Safety Medical Director - Global Safety Officer, Oncology
Amgen —Remote
- $256,606.50 - $347,173.50 a year
- Remote
- Medicine
- Mentoring
- Senior level
- Disability insurance
- Health insurance
3d
Auditor - GVP
CSL Behring —King of Prussia, PA
- Full-time
- Up to 50% travel
- Bachelor of Science
- Mid-level
12d
Director of Pharmacovigilance & Safety
Hippocratic AI —Palo Alto, CA
- Full-time
- 7 years
- HIPAA
- Research
Chief Medical Safety Officer, Pharmaceutical Products
GE HEALTHCARE —Chicago, IL
- $240,000 - $360,000 a year
- Remote
- Medicine
- Microsoft Excel
- BC/BE
- Health insurance
- Dental insurance
Manager, Global Risk & Safety
Incyte Corporation —Wilmington, DE
- Microsoft Excel
- Microsoft Outlook
- English
2d
Associate Director, Safety Scientist
BeiGene —Remote
- $154,300 - $204,300 a year
- Full-time
- Medicine
- Computer literacy
- Databases
- Health savings account
- Employee stock purchase plan
Manager, Global Risk Management & Safety Surveillance Scientist
Incyte Corporation —Wilmington, DE
- English
- Travel
- Experience equivalent to degree accepted
2d
Associate Director, Pharmacovigilance/ Product Safety
Insmed Incorporated —Bridgewater, NJ
- $179,000 - $232,500 a year
- Full-time
- Medicine
- 3 years
- Travel
- Employee stock purchase plan
- Disability insurance
10h
Chief Medical Officer
insitro —South San Francisco, CA
- $450,000 - $480,000 a year
- Full-time
- Hybrid work
- Medicine
- 11+ years
- Office
- Paid parental leave
- Health insurance
Vice President, Associate General Counsel, Infectious Disease Franchise
Invivyd —New Haven, CT
- $309,000 - $383,000 a year
- Full-time
- Hybrid work
- HIPAA
- Research
- Office
Director, Central Statistical Monitoring
BeiGene —Remote
- $187,100 - $247,100 a year
- Full-time
- 5 years
- Master's degree
- Doctor of Philosophy
- Health savings account
- Employee stock purchase plan
Vice President, Clinical Development
Rigel Pharmaceuticals, Inc. —South San Francisco, CA
- $336,000 - $405,000 a year
- Full-time
- Hybrid work
- 8 years
- Travel
- Organizational skills
Quick Apply
Associate Director, Central Statistical Monitoring
BeiGene —Remote
- $162,600 - $212,600 a year
- Full-time
- Master's degree
- Doctor of Philosophy
- Senior level
- Health savings account
- Employee stock purchase plan
Vice President, Quality
Remix Therapeutics —Boston, MA
- $293,000 - $358,000 a year
- Master's degree
- Training & development
- Senior level
Quick Apply
Vice President, Pharmacovigilance
Crescent Biopharma —Waltham, MA
- $323,000 - $357,000 a year
- Full-time
- Medicine
- Bachelor of Science
- 11+ years
- Paid holidays
- Disability insurance
Quick Apply
7h
Training and Change Management Consultant – eClinical Systems
Cloudbyz —Naperville, IL
- Full-time
- 7 years
- Salesforce
- Education
GPS Case Management Medical Review Therapeutic Area Leader
Eli Lilly —Indianapolis, IN
- $225,000 - $330,000 a year
- Full-time
- Medicine
- BC/BE
- English
- Health insurance
- Dental insurance
13d
Signal Management Expert
Sanofi —Cambridge, MA
- $122,250.00 - $176,583.33 a year
- English
- Mid-level
- Bachelor's degree
- Parental leave
14d

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Global Safety Officer

Sanofi -
Cambridge, MA

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Job Details

$178,500 - $297,500 a year

Benefits

Parental leave

Qualifications

Medical writing
Doctor of Medicine
Committee work
Medicine
Patient safety data management
Pharmacovigilance research
Clinical trial risk management
BC/BE
English
3 years
Collaboration with product development teams
Analysis skills
Research report preparation
Clinical data report preparation
Epidemiology
Document review
Leading team collaboration initiatives
Regulatory submission editing and review
Communication with regulatory authorities for clinical trials
Safety and toxicology data reporting
Senior level
Clinical program risk management
Clinical data analysis
Project leadership
Experience conducting due diligence within healthcare
Cross-functional team management
Negotiation
Cross-functional communication

Full Job Description

Job title: Global Safety Officer

Location: Cambridge, MA / Morristown, NJ

About the job

Join the engine of Sanofi’s mission — where deep immunoscience meets bold, AI-powered research. In R&D, you’ll drive breakthroughs that could turn the impossible into possible for millions.

About Sanofi

We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.

Main Responsibilities:

In this role you will be active in five main areas

Internal & External Safety Expert

Provide PV and risk management expertise to internal and external customers
Safety expert for product
Maintain knowledge of product, product environment, and recent literature
Maintain PV expertise, and understanding of international safety regulations and guidelines
Lead cross functional Safety Management Teams (SMTs) and GPE internal Safety Analysis Teams (SATs)
Communicate with and represent PV position within project/product teams, with external partners, key opinion leaders, and Health Authorities, and during internal and external negotiations
Provide strategic and proactive safety input into development plans
Support due diligence activities and pharmacovigilance agreements

Signal Detection & Assessment

Responsible for signal detection and analysis
Collaborate with Center of Excellence for Signal Detection and Data Mining and Safety Epidemiology group
Identify and implement proactive safety analysis strategies to further define the safety profile
Lead aggregate safety data review activities and coordinate safety surveillance activities

Risk Assessment/Risk Management/Benefit-Risk Assessment

Provide proactive risk assessment
Co-lead benefit-risk assessment with other relevant functions
Develop risk management strategies and plans and monitor effectiveness
Collaborate with Center of Excellence for Risk Management and Safety Epidemiology

Submission Activities

Represent safety position in cross functional submission teams
Ensure generation, consistency, and quality of safety sections in submission documents
Write responses or contributions to health authorities’ questions
Support preparation and conduct of Advisory Committee meetings

Report Writing

Document, coordinate, review and validate Periodic reports, e.g.: RMP update, IND Annual Report, Annual Safety Report/Development Safety Update Report, Periodic Safety Update Report
Serve as the medical safety expert to the GPE Periodic Reports group for assigned projects and products

About You

Qualifications/Education & Work Experience:

M.D. Degree or equivalent
For MD, Board Certified/Board eligible, or equivalent, is preferred
Minimum 3 years' total experience in international pharmacovigilance, or equivalent relevant industry experience (e.g. clinical development) with relevant clinical experience considered. Exceptionally, candidates may be considered if they have proven excellence in a similar prior position, even if they have less than 3 years international PV experience

Competencies:

Excellent clinical judgment
Capability to synthesize and critically analyse data from multiple sources
Ability to communicate complex clinical issues and analysis orally and in writing
Able to develop and document sound risk assessment
Demonstrates initiative and capacity to work under pressure
Demonstrates leadership within cross-functional team environment
Excellent teamwork and interpersonal skills are required
Fluent in English (written and spoken)

Why Choose Us?

Bring the miracles of science to life alongside a supportive, future-focused team.
Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.

Sanofi US Services and its U.S. affiliates are Equal Opportunity employers committed to a culturally inclusive workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

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All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.

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Refine Your Search

global safety officer pharmacovigilance jobs

Global Safety Officer

Global Safety Officer, I&I

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Chief Medical Safety Officer, Pharmaceutical Products

Manager, Global Risk & Safety

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Manager, Global Risk Management & Safety Surveillance Scientist

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Vice President, Clinical Development

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GPS Case Management Medical Review Therapeutic Area Leader

Signal Management Expert

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