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Bristol Myers Squibb
Senior Manager, Patient Safety ScientistBristol Myers Squibb • Uxbridge, England, UK
Senior Manager, Patient Safety Scientist

Senior Manager, Patient Safety Scientist

Bristol Myers Squibb • Uxbridge, England, UK
27 days ago
Job type
  • Full-time
Job description

Working with Us
Challenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the latest breakthroughs in cell therapy this is work that transforms the lives of patients and the careers of those who do it. Youll get the chance to grow and thrive through opportunities uncommon in scale and scope alongside high-achieving teams. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits services and programs that provide our employees with the resources to pursue their goals both at work and in their personal lives. Read more: Safety Your Science

At Bristol Myers Squibb were driven by a single mission: to discover develop and deliver innovative medicines that help patients prevail over serious diseases. Behind every medicine we bring to patients is a team of experts committed to keeping them safe and were looking for a talented pharmacovigilance professional to join that team.

The Role

AsSenior Manager Patient Safety Science youll be at the heart of how BMS characterises and protects the safe use of its medicines. Working closely with Medical Safety Assessment Physicians and Safety Management Teams youll own signal detection lead safety data review meetings drive risk management strategies and ensure robust pharmacovigilance compliance across the product lifecycle from early development through to postmarketing.

This is a high-impact role with real autonomy cross-functional visibility and the opportunity to shape benefit-risk decisions on medicines that matter.

What Youll Do
  • Detect & Manage Signals Lead quantitative signal detection author comprehensive signal reports and escalate issues that could impact key safety milestones
  • Drive Safety Surveillance Prepare and contribute to aggregate safety documents (DSURs PBRERs PADERs) and respond to health authority queries
  • Support Clinical Development Contribute to safety sections of protocols investigator brochures CSRs and informed consent forms
  • Shape Regulatory Submissions Author safety sections of MAAs including ISS SCS clinical overviews and product labelling (USPI CCDS SmPC)
  • Lead Risk Management Develop and maintain global and EU Risk Management Plans additional Risk Minimisation Measures and Post-Authorisation Safety Studies
  • Champion Innovation Leverage AI automation and digital platforms to continuously improve safety workflows and data analysis

What Youll Bring

Education:Scientific degree (BS MS PharmD PhD MD RN or equivalent)

Experience:46 years in pharmacovigilance drug development or the pharmaceutical industry

Skills & Attributes:

  • Solid grounding in global pharmacovigilance regulations and postmarketing safety requirements
  • Strong analytical mindset with the ability to interpret complex clinical nonclinical and real-world safety data
  • Excellent organisational skills with the ability to manage competing timelines without compromising quality
  • A collaborative adaptable communicator who thrives in cross-functional environments
  • Comfort working with emerging technologies including AI and digital safety tools

#LI-Hybrid

If you come across a role that intrigues you but doesnt perfectly line up with your resume we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work Life-changing Careers
With a single vision as inspiring as Transforming patients lives through science every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture promoting global participation in clinical trials while our shared values of passion innovation urgency accountability inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential site-by-design field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles onsite presence is considered an essential job function and is critical to collaboration innovation productivity and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application or in any part of the recruitment process direct your inquiries to . Visit to access our complete Equal Employment Opportunity statement.

Bristol Myers Squibb is Disability Confident Employer

A UK Government scheme

Candidate Rights

BMS will consider for employment qualified applicants with arrest and conviction records pursuant to applicable laws in your area.

Data Protection

We will never request payments financial information or social security numbers during our application or recruitment process. Learn more about protecting yourself at data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

If you believe that the job posting is missing information required by local law or incorrect in any way please contact BMS at . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.

R: Senior Manager Patient Safety Scientist


Required Experience:

Senior Manager


Employment Type : Full-Time
Experience: years
Vacancy: 1
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Senior Manager, Patient Safety Scientist • Uxbridge, England, UK

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