439394
Business Introduction

At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success. We’re uniting science, technology, and talent to get ahead of disease together.

Find out more:

Our approach to R&D
This position supports the HIV Therapeutic Area.
Position Summary
Responsible to lead medical and scientific staff within the SERM (Safety Evaluation & Risk Management) group and defining and driving the strategy and vision of clinical safety and pharmacovigilance activities in alignment with Global Safety business strategies.
As a senior member of the Global Safety organization the role is responsible to:
*Lead and line manage the SERM group (10 team members) responsible for marketed HIV assets with on going clinical development from first-time-in-human studies through to regulatory submission. Line Management leadership competencies include resource and team management, coaching, influencing others, collaborative working, decision making, change management, partnership, and relations management.
*Implement policy, processes and support the implementation of operational and strategic plans
*Ensure 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.
Key Responsibilities
Scientific/Medical Knowledge PV Expertise
*Expert in clinical safety and pharmacovigilance activities.
*Demonstrated record of sound judgement and decision making in safety evidence generation, benefit-risk assessment, causality assessment, evaluation of safety signals, and of proactive risk management strategies including management of labelling changes, physician and patient education and monitoring of safety issues in the real world.
*Coaches and mentors SERM colleagues in the scientific/medical aspects of signal evaluation methodology and risk management and preparation of regulatory safety reports and other documents.
*Demonstrated track record of quality decision making and creative problem resolution in critical situations, based on assessment of all relevant supporting and conflicting information/factors and understanding of the wider context.
*Provides excellent medical/scientific judgment, strong analytical skills, proactive approach in drug safety and high sense of urgency.
*Champions/sponsors safety governance by development of safety strategy and its execution for products in clinical development and post marketing settings. Anticipates, detects and addresses product safety issues and ensures that risk-reduction strategies are implemented appropriately.
*Leads cross-GSK activities such as safety advisory panels, interfaces with and assumes ad hoc membership of a Senior Governance Committee.
*Ability to engage in, and contribute to, broad GSK environment and pharmacovigilance environment outside GSK with confidence, impact, integrity and professionalism.
Cross-functional Matrix team leadership
*Proven ability to affect department, or product strategies with a strong understanding and ability to incorporate global considerations into decision making.
*Builds strong collaborative relationships and displays excellent leadership skills on safety issues whilst working in a matrix team, with an outstanding track record leading a team in a matrix setting.
*Demonstrates resilience and ability to adjust behaviours and priorities based on changing environment.
*Leads or oversees SERM contribution to due diligence activities.
Communications (verbal, written) and Influencing (internal PV Governance and External LTs)
*Excellent communication (verbal, written) and influencing (internally and externally) skills.
*Leads cross-GSK activities such as safety advisory panels, interfaces and assumes ad hoc membership of a Senior Governance Committee. Influences others external to GSK to meet organisational objectives and may be recognised as a key player in external international pharmacovigilance activities (i.e., may be a member of trade association or external initiatives).
*Leads driving change until their implementation.
*Recognised as an authority with expert knowledge of relevant pharmacovigilance regulations and methodologies applicable to SERM activities.
Why you?Basic Qualifications:We are looking for professionals with these required skills to achieve our goals:
*Medical degree for Senior Medical Director or Health Sciences/Health Care Professional degree (e.g., BSc, MS, PhD, RN/BSN/MSN, NP, RPh/B Pharm/Pharm D) for Senior Scientific Director
*For Senior Medical Director - Completion of a formal postgraduate clinical training, clinical residency or specialty training
*Comprehensive experience in the Pharmaceutical or Biotech industry working in Pharmacovigilance or Drug Safety
*Significant 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.
*Prior experience in the HIV therapy area is desirable but not essential
Working pattern and location
*This role is based in the United Kingdom.
*The role is hybrid, combining office presence with remote work to support collaboration and flexibility.
What you will gain

You will have direct impact on patient safety and on the scientific approach we take to benefit-risk decisions. You will grow your leadership skills and expand your influence across scientific, regulatory and clinical stakeholders. We welcome applicants from all backgrounds and encourage people who want a collaborative and inclusive environment to apply.
How to apply

If this role resonates with your experience and ambitions, we would like to hear from you. Please submit your CV and...