# SERM Scientific Director, HIV

**Company**: GSK
**Location**: London, New Oxford Street
**Work arrangement**: hybrid
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

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## Description

The SERM Scientific Director, HIV will provide 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.

Responsibilities include:

**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.

- Demonstrates highly developed multi-tasking skills, ability to prioritise tasks and consistently delivers on deadlines.

**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.

- Facilitates safety governance/SRTs in the clinical development and post marketing settings.

- Represents GS on cross-functional Clinical Matrix Teams and/or Project Teams.

- Leads or participates in cross-functional process initiatives and/or Process Workstreams.

**Communications and Influencing**

- Leads presentations on recommendations or safety issues to senior staff members.

- Has the skillset to interact with confidence, credibility, and influence at all levels of the GSK organisation.

- Excellent communication (verbal, written) and influencing (internally and externally) skills.

**Requirements**

- PhamD or PhD required

- Advanced experience in the Pharmaceutical or Biotech industry working in Pharmacovigilance, or Drug Safety

- Significant pharmacovigilance experience relating to Safety Evaluation and Risk Management

- Experience with Signal Detection and safety surveillance

- Knowledge/experience of international pharmacovigilance requirements and drug development and approval processes.

- Experience working in large matrix organizations

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## Skills

### Required
- Pharmacovigilance
- Risk Management
- Clinical Development
- Post-Marketing
- Signal Detection
- Safety Surveillance
- International Pharmacovigilance Requirements

### Nice to have
- Infectious Diseases
- HIV Assets
- Regulatory Submissions
- Periodic Safety Reports
- Epidemiology
- Biostatistics
- Real-World Evidence

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