Executive Director, Global Patient Safety Sciences Delivery in London

Executive Director, Global Patient Safety Sciences Delivery in London

London Full-Time 100000 - 150000 £ / year (est.) No working from home possible
BioSpace

At a Glance

  • Tasks: Lead global patient safety operations and drive innovative strategies for life-changing medicines.
  • Company: Join Regeneron, a leader in science and innovation for serious diseases.
  • Benefits: Competitive salary, bonuses, health benefits, and a supportive work culture.
  • Other info: Inclusive workplace with excellent career growth opportunities.
  • Why this job: Make a real impact in patient safety while developing your leadership skills.
  • Qualifications: M.D., Ph.D., or PharmD with 17+ years in the pharmaceutical industry.

The predicted salary is between 100000 - 150000 £ per year.

At Regeneron, we use science and innovation to develop life‑changing medicines for people with serious diseases. We are seeking an Executive Director to join our Patient Safety team. The Executive Director, Global Patient Safety Sciences Delivery serves as the key point of contact for all Safety Sciences operations and risk‑related responsibilities across all Therapeutic Areas (TAs). This role is responsible for driving consistency across the portfolio for standard activities performed by the Safety Scientists (e.g., data transformation, safety surveillance, SMT preparation, early draft of aggregate reports, signal evaluations, label enhancement justifications), for establishing and maintaining the processes and written procedures that underpin safety governance and other fundamental Safety Sciences functions, and for leading the development and management of their team. The role requires cross‑functional collaboration with Safety Sciences TAHs and other leaders and is a member of the GPS Leadership Team (GPS LT).

When & Where

Work Location: Uxbridge, UK
Travel: As needed

Discover Your Role

  • Define the strategy to ensure standardization and consistency in the execution of core activities (e.g., signal detection, authoring sections for safety documents) across all products and TAs through development of common practices, processes, templates.
  • Oversee relevant training programs for GPS Safety Sciences, including a standardized training curriculum, proficiency matrix, and knowledge management repository.
  • Enable the Global Capability Center (GCC) to operate more efficiently and at scale with the demands of the business.
  • Develop innovative approaches to delivering on core activities that integrate new technologies, including AI.

Operational Delivery Oversight

  • Ensure compliance and quality management of Safety Sciences Operations activities, including compliance with all regulations and establishment of SOPs and associated monitoring tools.
  • Oversee all aspects of signal detection coordination and signal management process across all TAs, including Safety Monitoring Team (SMT), Safety Surveillance Plan (SSP) and Signal Evaluation Report (SER).
  • Coordinate and support high‑quality, timely, and compliant delivery of benefit‑risk assessment for periodic safety reports (e.g., DSURs, PSURs) and support Safety Sciences Strategy in contributing medical and safety perspective to the GPS portfolio of documents (e.g., ARM, RMP, SMP) where required.
  • Set and oversee the framework for aggregate safety data analysis to ensure effective coordination and delivery.

Cross‑Functional Partnership

  • Serve as strategic point of contact to enable SS operational delivery in partnership with TAHs and GPS Leads.
  • Partner with key Regeneron interfaces (e.g., Clinical, Regulatory, Med Affairs, Biostats & Data Management).

Talent Development & Organizational Leadership

  • Build, coach, and scale a high‑performing team, and drive succession planning and talent pipelines.
  • Lead talent strategy and leadership development initiatives that strengthen capabilities across the organization.

This Role Requires

  • Minimum M.D., P.A., Ph.D. or PharmD Degree; Board Certification or equivalent in a relevant clinical specialty; MBA is an advantage.
  • 17+ years total experience in PV or relevant clinical experience in the pharmaceutical industry.
  • 6+ years of leading a team and people‑management experience.
  • Preferred experience with oversight of operations within a global patient safety organization.
  • Strong attention to detail with the ability to assess and optimize Safety operations processes, drive consistency, and ensure high‑quality, compliant execution across activities.
  • Strong leadership capabilities and presence, interpersonal, verbal and written communication skills, organizational and workload planning skills, and the ability to manage multiple projects simultaneously.

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture.

Executive Director, Global Patient Safety Sciences Delivery in London employer: BioSpace

At Regeneron, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters innovation and collaboration in the heart of Uxbridge, UK. Our commitment to employee growth is evident through comprehensive training programmes and leadership development initiatives, ensuring that our team members thrive in their careers while contributing to life-changing medicines. With a competitive benefits package and a focus on inclusivity, Regeneron is dedicated to creating a rewarding environment for all employees.

BioSpace

Contact Details:

BioSpace Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Executive Director, Global Patient Safety Sciences Delivery in London

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We think you need these skills to ace Executive Director, Global Patient Safety Sciences Delivery in London

Patient Safety Sciences
Signal Detection
Safety Surveillance
Data Analysis
Regulatory Compliance
Standard Operating Procedures (SOPs)
Team Leadership

Some tips for your application 🫡

Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at BioSpace!

Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show BioSpace that you're not just a fit for the job but also a safety-conscious candidate!

Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at BioSpace!

Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At BioSpace, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.

How to prepare for a job interview at BioSpace

Understand the Science

Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at BioSpace that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.

Showcase Relevant Experience

If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.

Know Their Products

Take some time to familiarise yourself with BioSpace’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.

Be Ready for Regulatory Scenarios

In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.