# Associate Medical Director, Safety Evaluation and Risk Management (SERM)

**Company**: GSK
**Location**: Durham
**Work arrangement**: hybrid
**Experience**: senior
**Job type**: full-time
**Salary**: PLN 0 to PLN 0, EUR 87,000 to EUR 145,000
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://gsk.wd5.myworkdayjobs.com/en-US/GSKCareers/job/Durham-300-Morris-Street/Associate-Medical-Director--Safety-Evaluation-and-Risk-Management--SERM-_444801?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_c550257e-3a6

## Description

As Associate Medical Director, Safety Evaluation and Risk Management (SERM), you will provide medical/scientific expertise in the safety evaluation and risk management of GSK assets in clinical development and/or the post-marketing setting.

You will contribute to clinical safety and pharmacovigilance strategy for assets within Global Safety, collaborating with senior governance and partner teams to drive evidence-based safety decisions.

Key Responsibilities:

- Provide medical leadership across clinical programs, contribute to clinical trial design, safety oversight, and scientific communication.

- Work closely with cross-functional teams including Clinical Operations, Safety, Regulatory, Biostatistics, and Commercial.

- Ensure scientifically sound review and interpretation of data and management of safety issues.

- Escalate safety issues identified through the safety review process to senior management and safety governance as appropriate.

Basic Qualification:

- Medical degree, with completion of a formal postgraduate clinical training, residency or specialty training.

- Experience in the pharmaceutical or biotechnology industry working in pharmacovigilance or drug safety.

- Experience in clinical safety and pharmacovigilance activities, including evidence generation, benefit–risk assessment, causality assessment and evaluation of safety signals.

Preferred Qualification:

- Proven record of high-quality, timely decision-making and creative problem-solving in complex or critical safety situations.

- Experience leading or contributing to safety governance activities, such as safety advisory panels and senior governance committees.

- Experience with successful global regulatory filings.

Working arrangement:

- This role is hybrid, with flexibility to work on-site 2 to 3 days per week.

## Skills

### Required
- Clinical Development
- Communication
- Drug Regulatory Affairs
- Evidence Based Decision Making
- Good Clinical Practice (GCP)
- Influencing Without Authority
- Learning Agility
- People Management
- Project Management
- Scientific Presentations
- Strategic Thinking

### Nice to have
- Proven record of high-quality, timely decision-making
- Experience leading or contributing to safety governance activities
- Experience with successful global regulatory filings
- Recognised expertise in pharmacovigilance regulations and methodologies

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