# SERM Associate Scientific Director

**Company**: GSK
**Location**: London, New Oxford Street
**Work arrangement**: hybrid
**Experience**: senior
**Job type**: full-time
**Salary**: PLN 318,000 to PLN 530,000
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://gsk.wd5.myworkdayjobs.com/en-US/GSKCareers/job/UK--London--New-Oxford-Street/SERM-Associate-Scientific-Director_451214-2?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/job/serm-associate-scientific-director-f7394804-3f2/

## Description

Join GSK as a SERM Associate Scientific Director in the United Kingdom and use your medical and scientific expertise to support patient safety worldwide.

You will work closely with cross-functional teams to evaluate safety data and manage risks across key products in clinical development and the post-marketing setting.

Your clear, thoughtful insights will help shape decision-making and improve outcomes for patients and healthcare professionals.

Responsibilities:

- Lead or contribute signal detection and evaluation activities for assigned products, applying strong scientific judgment.

- Prepare and review global regulatory reports and risk management plans, ensuring accuracy and timely delivery.

- Support safety governance meetings and collaborative safety review teams for clinical and post-marketing safety oversight.

- Contribute to the design and implementation of risk-reduction strategies in clinical protocols and product information.

- Build and maintain effective relationships across teams, providing clear communication and mentoring colleagues where appropriate.

- Participate in process improvements to enhance compliance, quality, and efficiency within safety evaluation activities.

Basic Qualifications:

- A degree in Health Sciences or Healthcare Professional qualification (for example, BSc, MSc, PhD, RN, NP, PharmD).

- Practical experience in pharmacovigilance focusing on safety evaluation and risk management during clinical development and post-marketing phases.

- Understanding of international pharmacovigilance guidelines and drug development and approval processes.

- Experience working effectively in cross-functional, matrix teams.

- Strong scientific writing skills with the ability to prepare detailed safety evaluations and regulatory documents.

- Ability to manage multiple tasks with attention to detail and deliver high-quality results on time.

Preferred Qualifications:

- Advanced degree (e.g., PhD, MD, or equivalent).

- Previous experience working in large, global pharmaceutical organizations.

- Familiarity with early clinical development safety activities.

- Experience contributing to safety governance and regulatory inspections or audits.

- Knowledge of relevant safety databases and data visualisation tools.

- Comfortable working in a hybrid model that combines remote and on-site work.

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## Skills

### Required
- Pharmacovigilance
- Scientific Writing
- Risk Management
- Safety Evaluation
- Regulatory Compliance

### Nice to have
- Advanced degree
- Global Pharmaceutical Organizations
- Early Clinical Development Safety
- Safety Governance
- Data Visualisation Tools

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