# Interventional Study Scientist Medical Director

**Company**: GSK
**Work arrangement**: hybrid
**Experience**: senior
**Job type**: full-time
**Salary**: $187,275 to $312,125
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://gsk.wd5.myworkdayjobs.com/en-US/GSKCareers/job/UK--London--New-Oxford-Street/Interventional-Study-Scientist-Medical-Director_445036-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_4fd7a23f-85b

## Description

Join GSK's Medical Affairs team as an Interventional Study Scientist Medical Director. You'll lead the scientific design and execution of interventional clinical studies, ensuring studies are conducted with the highest standards of quality and ethics.

Responsibilities:

- Design and oversee interventional clinical studies, ensuring alignment with strategic objectives and evidence plans.

- Facilitate medical governance, review safety data, and guide risk mitigation actions.

- Provide scientific oversight for study protocols, analysis plans, and interpretation of study data.

- Ensure patient safety and scientific integrity throughout study conduct.

- Collaborate with cross-functional teams to deliver impactful results.

- Prepare and present study results for scientific meetings, publications, and regulatory submissions.

- Engage with internal and external stakeholders to enhance study design and execution.

Requirements:

- Advanced degree in a relevant scientific discipline (MD, PhD, PharmD, or equivalent).

- Substantial experience leading interventional clinical studies in a therapeutic area.

- Proven experience designing and executing clinical trials with demonstrated impact.

- Strong understanding of regulatory requirements and industry best practices for clinical research.

- Excellent communication and organizational skills.

Preferred Qualifications:

- Experience leading global Phase IIIb/IV interventional studies.

- Experience collaborating with regulatory authorities.

- Familiarity with innovative approaches in clinical trial design and execution.

- Exposure to working with key opinion leaders, investigators, and external partners.

- Experience developing scientific content for publications and regulatory submissions.

- Understanding of digital tools and methodologies for evidence generation.

- Experience leading cross-functional teams in a matrixed environment.

Benefits:

- Annual base salary ranging from $187,275 to $312,125.

- Annual bonus and eligibility to participate in share-based long-term incentive program.

- Health care and other insurance benefits.

- Retirement benefits.

- Paid holidays, vacation, and paid caregiver/parental and medical leave.

## Skills

### Required
- clinical research
- regulatory requirements
- scientific oversight
- patient safety
- communication skills

### Nice to have
- global Phase IIIb/IV interventional studies
- regulatory authorities
- innovative approaches
- digital tools
- cross-functional teams

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