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SERM Medical Director, Oncology

GSK

London

On-site

GBP 60,000 - 100,000

11 days ago

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Job summary

An established industry player is seeking a dedicated professional to provide medical and scientific expertise in safety evaluation and risk management. This role focuses on ensuring patient safety through effective pharmacovigilance and risk management strategies. The ideal candidate will lead cross-functional teams, contribute to global regulatory submissions, and communicate safety issues to senior management and external stakeholders. Join a dynamic environment where innovation thrives, and help make a significant impact on global health outcomes while fostering a culture of inclusion and growth.

Qualifications

  • Strong background in pharmacovigilance and risk management.
  • Experience in clinical settings and international pharmacovigilance requirements.

Responsibilities

  • Lead pharmacovigilance and risk management planning for clinical products.
  • Develop safety strategies and execute governance for product safety issues.
  • Communicate safety recommendations to senior staff and regulatory authorities.

Skills

Pharmacovigilance

Risk Management

Analytical Thinking

Decision Making

Leadership

Communication Skills

Problem Resolution

Education

Primary medical qualification (MBBS or equivalent)

Specialty training (CCT and fellowship or equivalent)

PhD/PharmD or MPH (preferred)

Job description

Job Purpose

Provides in-depth medical/scientific expertise in the safety evaluation and risk management of key GSK assets or 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.

Key Responsibilities
Scientific/Medical Knowledge PV Expertise
  • Leads Pharmacovigilance and Risk Management Planning and develops strategy for approach to evaluation of issues in the clinical matrix.
  • Leads the safety component of global regulatory submissions.
  • Expert evaluation skills and analytical thinking for literature review, clinical data synthesis, analysis and interpretation.
  • Demonstrated track record of quality decision making and creative problem resolution, based on assessment of all relevant supporting and conflicting information/factors and understanding of the wider context.
  • Demonstrates highly developed multi-tasking skills, ability to prioritise tasks and consistently delivers on deadlines, with high performance standards for quality.
  • Explores positions and alternatives to reach mutually beneficial agreements and solutions.
Cross-functional Matrix team leadership
  • Leads 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 (e.g., product incidents) and ensures that risk-reduction strategies are implemented appropriately.
  • 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.
  • Represents GS on cross-functional Clinical Matrix Teams and/or Project Teams. Leads cross-functional ad hoc teams to address urgent and important product safety issues.
  • 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.
  • Authors/participates in written standard updates (e.g., SOPs) to ensure policies and regulations are being adhered to correctly and consistently.
  • Accountable for the escalation of issues and communication on safety matters (e.g., GSB, CHSLC, GLC, QPPV).
  • Builds strong working relationships and displays excellent leadership skills on safety issues whilst working in a matrix team, with a demonstrated ability to lead a team in a matrix setting. Ability to coach and mentor others.
Communications (verbal, written) and Influencing (internal PV Governance and External LTs)
  • Leads presentations on recommendations or safety issues to senior staff members at the GSK Senior Governance Committees. Has the skillset to interact with confidence, credibility, and influence at all levels of the GSK organisation. In addition, is expected to represent GSK and contribute to safety related discussions at meetings with regulatory authorities, outside consultants and other companies such as licensing partners.
  • Leads cross-functional process improvement team within GSK. Thinks tactically/strategically and takes account of the internal and external environment when considering safety issues and changes to SERM processes or business improvements. Contributes to development of long-term strategy for clinical programs. Regularly contributes innovative ideas to address new issues or improve approaches to existing operations.
  • Leads inspection readiness and prepared as needed to support audits/inspections.
  • Excellent communication (verbal, written) and influencing (internally and externally) skills.
Basic Qualifications:

We are looking for professionals with these required skills to achieve our goals:
  • Primary medical qualification (MBBS or equivalent) and completion of Specialty training (CCT and fellowship or equivalent level)
  • Experience, at least, within a Clinical background/setting
  • Experience of international pharmacovigilance requirements (e.g., ICH, GVP modules, CIOMS initiatives) and drug development and approval processes.
Preferred Qualifications:
  • PhD/PharmD or MPH in addition to medical degree and registration/certification
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.
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