SERM Medical Associate Director
SERM Medical Associate Director

SERM Medical Associate Director

London Full-Time 48000 - 84000 Β£ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead safety evaluations and risk management for GSK's clinical assets.
  • Company: GSK is a global biopharma company focused on advancing health through science and technology.
  • Benefits: Enjoy a collaborative culture, opportunities for growth, and a focus on wellbeing.
  • Why this job: Make a real impact on patient safety while working in a dynamic, innovative environment.
  • Qualifications: Medical Doctor or equivalent with experience in pharmacovigilance and drug development.
  • Other info: Join us to thrive in a diverse and inclusive workplace.

The predicted salary is between 48000 - 84000 Β£ per year.

Site Name: Belgium-Wavre, UK – London – New Oxford Street
Posted Date: Jul 9 2025

About the role

Provides medical/scientific expertise in the safety evaluation and risk management of key GSK assets in clinical development and/or the post-marketing setting.

Ensures scientifically sound review and interpretation of data and management of safety issues and escalates safety issues identified through the safety review process to senior management and safety governance as appropriate. Makes recommendations for the further characterization, management, and communication of safety risks.

Focus on efficiency and effectiveness to meet the needs of our Patients and HCPs.Supporting the pharmacovigilance and benefit-risk management of the assigned portfolio of GSK global assets to ensure Patient Safety globally.

If appointed as a manager (i.e., Team/Group Leader) is responsible for leadership of a team of individual contributors. Line Management (including functional matrix reports) leadership competencies include resource and team management, coaching, influencing others, collaborative working, decision making, change management, partnership, and relations management.

About the responsibilities

1.Scientific/Medical Knowledge PV Expertise

  • Responsible for signal detection and evaluation activities for assigned products.
  • Drives production of regulatory periodic reports and associated documentation and RMPs globally according to the agreed process and timelines; advises on content of regulatory period reports (in partnership with the product physician).
  • Authors the SERM safety contribution to global regulatory submissions in partnership with the product physician.
  • May respond to auditors/inspectors’ requests for information/additional information and completes corrective and preventative actions (CAPAs) within agreed timelines.
  • Advanced evaluation skills and analytical thinking for literature review, data gathering, data synthesis, analysis and interpretation.
  • Makes sound decisions based on relevant information or factors gathered from a broad range of sources, seeking help and input as needed. Identifies, evaluates, and recommends solutions to problems.
  • Committed to the task and able to prioritize activities effectively and meet multiple deadlines successfully and with appropriate attention to detail, setting high performance standards for quality.

2.Cross-functional Matrix team leadership

  • Supports and Facilitates safety governance/SRTs in the clinical development and post marketing settings by assisting in the establishment and operation of cross-functional teams in any SERM to detect and address product safety issues and ensures that risk-reduction strategies are implemented appropriately in clinical study protocols and/or product labelling.
  • Leads or participates in cross-functional process initiatives and/or Process Workstreams to drive efforts to improve adherence to regulations, data standards, quality, and efficiency.
  • May author/participate in written standard updates (e.g., SOPs) to ensure policies and regulations are being adhered to correctly and consistently.
  • Builds strong collaborative relationships and demonstrates good matrix leadership skills, proactively providing input to matrix teams on safety issues and processes. Ability to coach and mentor others.

3.Communications (verbal, written) and Influencing (internal PV Governance and External LTs)

  • Presents complex issues to senior staff members at the GSK Senior Governance Committees.
  • Demonstrates initiative and creativity in performing tasks and responsibilities. Proactively contributes ideas to improve existing operations.
  • Proactively contributes ideas to improve existing operations.
  • Participates in process improvement initiatives within GCSP and contributes to advancement of methodology and process by generating new ideas and proposals for implementation.
  • Possesses effective communication skills and is capable of presenting ideas and data clearly and concisely to a matrix team. Listens and responds appropriately to the views and feedback of others.
  • Robust medical/scientific writing skills are essential, as the preparation of detailed evaluations and reports on major GSK products is a core feature of the role.
  • Effective negotiation, influencing and persuasion to enable others in the matrix to understand own perspective.

About you

  • Medical Doctor (physician) preferred, (or equivalent e.g. veterinarian/dentist with appropriate PV experience), with additional relevant medical or scientific post-graduate qualifications.
  • Substantial experience in pharmacovigilance or drug development.
  • Pharmacovigilance experience relating to Safety Evaluation and Risk Management, encompassing both clinical development and post-marketing activities
  • Knowledge/experience of international pharmacovigilance requirements (e.g., ICH, GVP modules, CIOMS initiatives) and drug development and approval processes.
  • Experience working in large matrix organizations
  • Fluency in English

#LI-GSK

#GSKVaccines

If you have a disability and require assistance during the course of the selection process, you will have the opportunity to let us know what specific assistance you require in order to make suitable arrangements.

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).

Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK\’s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

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SERM Medical Associate Director employer: GlaxoSmithKline

GSK is an exceptional employer that prioritises the well-being and growth of its employees, fostering a collaborative and inclusive work culture in the vibrant locations of Belgium and the UK. With a strong focus on innovation in healthcare, GSK offers extensive opportunities for professional development, ensuring that team members are inspired and equipped to make a meaningful impact on global health. Join us to be part of a purpose-driven organisation where your contributions are valued and your career can thrive.
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Contact Detail:

GlaxoSmithKline Recruiting Team

StudySmarter Expert Advice 🀫

We think this is how you could land SERM Medical Associate Director

✨Tip Number 1

Familiarise yourself with the latest pharmacovigilance regulations and guidelines, especially those related to safety evaluation and risk management. This knowledge will not only help you in interviews but also demonstrate your commitment to staying updated in this rapidly evolving field.

✨Tip Number 2

Network with professionals in the pharmacovigilance and drug development sectors. Attend relevant conferences or webinars where you can meet industry experts and learn about current trends. Building these connections can provide valuable insights and potentially lead to referrals.

✨Tip Number 3

Prepare to discuss specific case studies or examples from your past experience that highlight your skills in signal detection, data analysis, and cross-functional team leadership. Being able to articulate your contributions to previous projects will set you apart during the interview process.

✨Tip Number 4

Showcase your communication skills by practising how to present complex medical information clearly and concisely. You might even consider conducting mock interviews with a friend or mentor to refine your ability to convey your ideas effectively, as this is crucial for the role.

We think you need these skills to ace SERM Medical Associate Director

Medical/Scientific Expertise
Pharmacovigilance Knowledge
Risk Management
Signal Detection and Evaluation
Regulatory Compliance
Data Analysis and Interpretation
Cross-Functional Team Leadership
Effective Communication Skills
Medical Writing Skills
Negotiation and Influencing Skills
Problem-Solving Skills
Attention to Detail
Project Management
Coaching and Mentoring
Knowledge of International Pharmacovigilance Requirements

Some tips for your application 🫑

Tailor Your CV: Make sure your CV highlights relevant experience in pharmacovigilance and drug development. Emphasise your medical qualifications and any specific projects that demonstrate your expertise in safety evaluation and risk management.

Craft a Strong Cover Letter: In your cover letter, clearly articulate why you are interested in the SERM Medical Associate Director position at GSK. Mention your understanding of their mission and how your skills align with their needs, particularly in relation to patient safety and cross-functional leadership.

Highlight Communication Skills: Given the importance of communication in this role, provide examples of how you've effectively communicated complex medical information in previous positions. This could include presentations to senior staff or contributions to regulatory submissions.

Showcase Leadership Experience: If you have experience leading teams or projects, make sure to highlight this in your application. Discuss your approach to coaching and mentoring others, as well as any successful initiatives you've led that improved processes or outcomes.

How to prepare for a job interview at GlaxoSmithKline

✨Showcase Your Medical Expertise

As a SERM Medical Associate Director, it's crucial to demonstrate your deep understanding of pharmacovigilance and risk management. Be prepared to discuss your previous experiences in safety evaluation and how you've contributed to patient safety in clinical development or post-marketing settings.

✨Highlight Cross-Functional Leadership Skills

This role requires strong matrix leadership abilities. Share examples of how you've successfully led cross-functional teams, facilitated safety governance, and implemented risk-reduction strategies. Emphasise your ability to coach and mentor others in these settings.

✨Prepare for Complex Communication Scenarios

Effective communication is key in this position. Be ready to present complex safety issues clearly and concisely to senior staff. Practice articulating your thoughts on safety evaluations and regulatory submissions, ensuring you can convey your ideas confidently.

✨Demonstrate Problem-Solving Skills

The ability to identify, evaluate, and recommend solutions to problems is essential. Prepare to discuss specific challenges you've faced in your career and how you approached them. Highlight your analytical thinking and decision-making processes, especially in high-pressure situations.

SERM Medical Associate Director
GlaxoSmithKline
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