At a Glance
- Tasks: Lead innovative drug development strategies and collaborate with top scientists in the field.
- Company: Join GSK, a global biopharma leader dedicated to advancing health.
- Benefits: Enjoy competitive salary, bonuses, health benefits, and flexible working options.
- Why this job: Make a real impact on patient health through cutting-edge research and development.
- Qualifications: PhD or MD in life sciences with experience in clinical pharmacology and drug development.
- Other info: Be part of a dynamic team focused on innovation and career growth.
The Department of Clinical Pharmacology Modelling & Simulation Respiratory and Inflammation (CPMS R&I) at GSK is recruiting a director-level Clinical Pharmacologist. This role is based in the UK or US, with remote working or placement at other European GSK sites possible for the right candidate.
Job Purpose
The Director, Clinical Pharmacology sits within the newly established Clinical Pharmacology and Quantitative Medicine (CPQM) organisation, which aims to be a centre of excellence in Model‑Informed Drug Development (MIDD) by integrating clinical pharmacology, digital medicine, translational imaging and mechanistic/systems modelling. You will lead the end‑to‑end application of MIDD across the drug development lifecycle—from first‑in‑human studies through filing and lifecycle management—and provide clinical pharmacology strategy and evidence‑generation input. This is an opportunity to join a highly regarded, high‑impact team with a strong publication track record, reporting directly to the Respiratory, Immunology & Inflammation Research Unit (RIIRU).
Main responsibilities
- Design & Execute Model Informed and Clinical Pharmacology strategies
- Ensure robust ways of working and regulatory ready evidence
- Build cross‑functional partnerships
- External engagement & scientific leadership
- Develop and implement robust MIDD & ClinPharm evidence strategies to de-risk and accelerate RIIRU programs.
- Aim for faster development, optimal dosing and stronger regulatory positioning across respiratory, inflammation, neurodegeneration and emerging areas — and support business development opportunities.
- Draft and review clinical pharmacology regulatory content to support timely approvals and optimal labelling.
- Maintain up to date knowledge of FDA, EMA, CDE, PMDA and ICH expectations and embed regulatory considerations and best practices into study design and MIDD strategies.
- Work closely with CPQM peers (digital medicine, translational imaging, MIDD specialists, mechanistic/systems modelling) and cross functional partners (biology, data science, computational biology, clinical, etc.).
- Maintain strong networks and share best practices in the CPMS community of practice.
- Build strong network key functions such as AI/ML, biomarkers, biostatistics, clinical operations, data science, computational biology and RWE to embed quantitative approaches into decision making at asset level.
- Raise GSK's profile in MIDD, clinical pharmacology, QSP and AI/ML integration through publications, conference presentations and active participation in scientific and regulatory fora to influence method adoption and regulatory dialogue.
Basic Qualifications
- PhD in life sciences or related discipline, MD, or PharmD, with experience in clinical pharmacology, modelling and simulation in pharmaceutical research and development.
- Significant experience in clinical pharmacology, modelling/simulation and drug development to solve practical problems in the pharmaceutical industry.
- Experience in pharmacometrics and their application to clinical questions in drug development.
Preferred Qualifications
- Additional experience in respiratory and immunology would be beneficial.
- Demonstrated experience of collaboration in a multi‑discipline team, using effective communication and taking personal accountability for timely delivery of results.
- Evidenced experience making sound judgement in complex situations and adapting to changing business needs by prioritising multiple tasks.
- Experience working with senior stakeholders in a cross functional environment.
- Track record of implementation of Model‑Informed Drug Discovery and Development (MIDD) approaches to accelerate patient access to novel therapies and to expand therapeutic indications of marketed drugs.
- Drive and learning agility to build knowledge on a drug‑disease system, symptom progression, standard of care, and trial design.
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases to impact health at scale. People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
Director Clinical Pharmacology in Stevenage employer: The Association of Technology, Management and Applied Engineering
Contact Detail:
The Association of Technology, Management and Applied Engineering Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Director Clinical Pharmacology in Stevenage
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical pharmacology field on LinkedIn or at industry events. Building connections can lead to insider info about job openings and even referrals.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of Model-Informed Drug Development (MIDD) and current trends in clinical pharmacology. We want to see you shine, so practice articulating your experience and how it aligns with the role.
✨Tip Number 3
Showcase your expertise! Consider writing articles or sharing insights on platforms like LinkedIn. This not only highlights your knowledge but also raises your profile in the industry, making you more attractive to potential employers.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we love seeing candidates who are proactive about their job search!
We think you need these skills to ace Director Clinical Pharmacology in Stevenage
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter for the Director, Clinical Pharmacology role. Highlight your experience in clinical pharmacology and modelling, and show how it aligns with our goals at StudySmarter.
Showcase Your Achievements: Don’t just list your responsibilities; share specific achievements that demonstrate your impact in previous roles. We love seeing quantifiable results that reflect your expertise in drug development and regulatory strategies.
Be Clear and Concise: Keep your application clear and to the point. Use straightforward language and avoid jargon where possible. We appreciate a well-structured application that makes it easy for us to see your qualifications.
Apply Through Our Website: We encourage you to apply directly through our website. This ensures your application is received promptly and allows us to process it efficiently. Plus, it’s the best way to stay updated on your application status!
How to prepare for a job interview at The Association of Technology, Management and Applied Engineering
✨Know Your Stuff
Make sure you have a solid understanding of clinical pharmacology, especially in relation to Model-Informed Drug Development (MIDD). Brush up on the latest FDA and EMA guidelines, as well as any recent advancements in respiratory and immunology fields. This will show that you're not just qualified, but genuinely passionate about the role.
✨Showcase Your Leadership Skills
As a director-level candidate, it's crucial to demonstrate your ability to lead cross-functional teams. Prepare examples of past experiences where you've successfully collaborated with diverse groups, highlighting your communication skills and how you’ve driven projects to completion. This will help the interviewers see you as a strategic leader.
✨Prepare for Scenario Questions
Expect to face scenario-based questions that assess your problem-solving abilities in complex situations. Think about challenges you've encountered in drug development and how you navigated them. Practising these scenarios can help you articulate your thought process clearly during the interview.
✨Network Like a Pro
Since building strong networks is part of the job, be ready to discuss how you've established connections in the industry. Mention any collaborations with AI/ML experts or biostatisticians, and how these relationships have enhanced your work. This shows that you understand the importance of networking in advancing drug development.