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- Tasks: Lead and manage innovative Clinical Pharmacology studies with a focus on participant safety and scientific quality.
- Company: Join Novartis, a leader in drug development and medical excellence.
- Benefits: Competitive salary, professional growth opportunities, and a collaborative work environment.
- Other info: Dynamic role with opportunities for strategic influence and career advancement.
- Why this job: Make a real impact on drug development and contribute to groundbreaking medical research.
- Qualifications: MD with PhD/post-doctoral training and significant experience in Clinical Pharmacology.
The predicted salary is between 80000 - 100000 ÂŁ per year.
As Associate Director, Translational Medicine Expert (TME), Clinical Pharmacology (CP TME), you will serve as the primary medical and scientific leader for FiH and Clinical Pharmacology studies. You will partner closely with cross‑functional Clinical Pharmacology Trial Teams, project‑level TMEs, and CRO collaborators to ensure the highest standards of medical supervision, participant safety, and scientific quality.
This role directly shapes early and full development programs across the BR portfolio and plays a critical part in delivering high‑quality data that informs program decisions and regulatory submissions. TM Clinical Pharmacology is a cross‑functional expert group responsible for the design, execution, and reporting of First‑in‑Human (FiH) and Clinical Pharmacology studies across all therapeutic areas. Operating through a strategic outsourcing model, we partner with qualified CROs while maintaining strong sponsor oversight of all strategic elements, including study design, regulatory engagement, and timelines.
Key Responsibilities
- Clinical Pharmacology Portfolio Leadership
- Lead and manage multiple FiH and Clinical Pharmacology studies simultaneously with medical, scientific, and operational excellence.
- Provide expert Clinical Pharmacology input into Study Concept Sheets, protocols, Informed Consent Forms, Statistical Analysis Plans, and TLF shells.
- Oversee medical and safety aspects of studies, including Site Initiation Visits, ongoing safety reviews, medical coding, and safety reporting.
- Drive development of Clinical Study Reports and contribute to dissemination of study results (e.g., abstracts, posters, manuscripts, plain‑language and technical summaries).
- Clinical Pharmacology Strategy & Cross‑Functional Collaboration
- Provide strategic Clinical Pharmacology guidance to ensure optimal study design aligned with program objectives.
- Partner with project‑level TMEs to align on compound background and program strategy.
- Lead or contribute to strategic initiatives, process optimization, and capability‑building efforts within TM Clinical Pharmacology.
- Strengthen collaborations with internal stakeholders across early and full development, as well as with external CRO partners.
Impact of the Role
- Enabling efficient and high‑quality execution of FiH and Clinical Pharmacology studies.
- Delivering key data supporting program milestones and regulatory submissions.
- Strengthening Clinical Pharmacology as a Novartis Center of Excellence across all BR therapeutic areas.
- Elevating scientific and medical expertise within TM and across development teams.
Essential Requirements
- Medical degree (MD) combined with a PhD/post‑doctoral training, board certification, or relevant Clinical Pharmacology research experience.
- Significant experience in FiH and Clinical Pharmacology studies—either in biotech/pharma, as a PI/sub‑investigator at a CRO, or at an academic medical center.
- Proven track record of contributions to drug development, regulatory submissions, or high‑quality scientific publications.
- Experience within a TM therapeutic area is an asset.
- Full professional proficiency in English (spoken and written).
Skills Desired
- Clinical Trials
- Data Analysis
- Data Monitoring
- Drug Development
- Drug Discovery
- Medical Strategy
- People Management
Associate Director, Translational Medicine Expert, TM Clinical Pharmacology in London employer: Novartis
Contact Detail:
Novartis Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Director, Translational Medicine Expert, TM Clinical Pharmacology in London
✨Tip Number 1
Network like a pro! Reach out to professionals in the Clinical Pharmacology field on LinkedIn or at industry events. A friendly chat can open doors and give you insights that might just land you that Associate Director role.
✨Tip Number 2
Prepare for interviews by diving deep into the latest trends in Translational Medicine. Show us you’re not just knowledgeable but passionate about the field. Bring your A-game with examples of how you've led studies or collaborated with teams.
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, drop a quick thank-you email to express your appreciation. It keeps you fresh in their minds and shows your enthusiasm for the position.
✨Tip Number 4
Apply through our website! We love seeing candidates who take the initiative. Plus, it gives you a chance to showcase your understanding of our values and mission right from the start.
We think you need these skills to ace Associate Director, Translational Medicine Expert, TM Clinical Pharmacology in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to highlight your experience in Clinical Pharmacology and FiH studies. We want to see how your background aligns with the role, so don’t be shy about showcasing relevant projects and achievements!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about this role and how your expertise can contribute to our team. Keep it concise but impactful – we love a good story!
Showcase Your Collaboration Skills: Since this role involves working closely with cross-functional teams, make sure to highlight your collaboration skills in your application. Share examples of successful partnerships or projects where teamwork made a difference.
Apply Through Our Website: We encourage you to apply through our website for a smoother process. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy!
How to prepare for a job interview at Novartis
✨Know Your Stuff
Make sure you brush up on your Clinical Pharmacology knowledge, especially around First-in-Human studies. Be ready to discuss your past experiences and how they relate to the role. This shows that you’re not just familiar with the theory but have practical insights to share.
✨Showcase Your Leadership Skills
As an Associate Director, you'll need to demonstrate your ability to lead cross-functional teams. Prepare examples of how you've successfully managed multiple projects or studies in the past, highlighting your strategic thinking and collaboration skills.
✨Prepare for Scenario Questions
Expect questions that put you in hypothetical situations related to study design or safety oversight. Think through potential challenges you might face in this role and how you would address them. This will show your problem-solving abilities and readiness for the position.
✨Engage with Your Interviewers
Don’t just answer questions—engage in a dialogue. Ask insightful questions about their current projects or challenges they face in Clinical Pharmacology. This demonstrates your genuine interest in the role and helps you assess if the company is the right fit for you.