Interventional Study Scientist Medical Director
GlaxoSmithKline Services Unlimited · GSK HQ · Remote · posted 16 days ago
Going rate £54,400UK median £55,519
Home Office going rates from
Occupation
2161Research and development (r&d) managers
Going rate for this occupation: £54,400 · UK median pay £55,519
Home Office going rates from
Where this salary sits
- UK pay for this occupation
- This role£67,332 to £87,020estimated · above the range ONS published
- Going rate£54,400
- UK median£55,519
View these figures as a table
| Percentile | Pay |
|---|---|
| 10th | £36,943 |
| 25th | £44,101 |
| 50th | £55,519 |
| 75th | £75,207 |
| Going rate | £54,400 |
| UK median | £55,519 |
Sponsorship
Sponsorship chance
Low
- Not matched to a licence on the register
- Occupation is eligible for Skilled Worker
- Estimated salary clears the going rate
On the public records we hold, sponsorship for this role looks unlikely: not matched to a licence on the register, and occupation is eligible for Skilled Worker.
- The salary is an estimate from national earnings data, not the employer's figure.
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Interventional Study Scientist Medical Director Locations
- GSK HQ UK, New Oxford Street & USA - Upper Providence/ Waltham MA
Reports to : Head of Interventional & Supported Studies Join GSK's Medical Affairs team and be part of a global organization that drives innovation, scientific excellence, and patient-centered solutions. At GSK, we are committed to improving lives by ensuring the safe and effective use of our medicines and vaccines, bridging critical scientific insights with impactful healthcare strategies. As a member of Medical Affairs organisation, you’ll collaborate with cross-functional teams to shape clinical practice, engage with healthcare professionals, and deliver on our promise to help people do more, feel better, and live longer. This role offers an exciting opportunity to lead the scientific design and execution of interventional clinical studies within the Medical Affairs organization. You will play a pivotal role in shaping data generation strategies, ensuring studies are conducted with the highest standards of quality and ethics, and collaborating with cross-functional teams to deliver impactful results. We are looking for a leader who is passionate about advancing science, thrives in a collaborative environment, and is motivated to make a meaningful impact on patient outcomes. In this role, you will: This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: 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, including medical governance and monitoring. Collaborate with cross-functional teams to ensure seamless execution and delivery of clinical programs. Prepare and present study results for scientific meetings, publications, and regulatory submissions. Engage with internal and external stakeholders, including investigators and thought leaders, to enhance study design and execution. Basic Qualifications & Skills We are seeking professionals with the following required skills and qualifications to help us achieve our goals: Advanced degree in a relevant scientific discipline (MD, PhD, PharmD, or equivalent). Substantial experience leading interventional clinical studies in a therapeutic area such as oncology/haematology/ Immunology, Specialty, and other GSK-related therapeutic areas of interest. Considerable experience in clinical research, including interventional studies. 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 & Skills 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. Why You? We are seeking candidates who want to grow into a visible scientific leader. This is a hybrid role based in either United Kingdom or United States with an expected in-office presence of around two to three days per week. You will have the opportunity to shape strategy, mentor colleagues, and influence clinical evidence generation across teams. We are committed to creating an inclusive workplace where everyone can thrive. If you are passionate about making a difference and have the skills and experience, we are looking for, we encourage you to apply. Please take a copy of the Job Description, as this will not be available post closure of the advert. When applying for this role, please use the ‘cover letter’ of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above. The information that you have provided in your cover letter and CV will be used to assess your application. Skills Digital Fluency, Enterprise Thinking, External Stakeholder Management, High Impact Communication, Launch Excellence, Patient Impact
Information from public records, not immigration advice.