Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Lead and manage innovative Clinical Pharmacology studies with a focus on participant safety and scientific quality.
- Company: Join Novartis, a leader in pharmaceutical innovation and development.
- Benefits: Competitive salary, professional growth opportunities, and a supportive work environment.
- Other info: Collaborative culture with opportunities for career advancement and personal development.
- Why this job: Make a real impact on drug development and regulatory submissions in a dynamic team.
- Qualifications: Medical degree with significant experience in Clinical Pharmacology studies.
The predicted salary is between 80000 - 100000 £ 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
- This role significantly influences the success of the Novartis development pipeline by:
- 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).
Why Novartis:
Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally.
Associate Director, Translational Medicine Expert, TM Clinical Pharmacology employer: Novartis Farmacéutica
Contact Detail:
Novartis Farmacéutica Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Director, Translational Medicine Expert, TM Clinical Pharmacology
✨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 lead to opportunities that aren’t even advertised yet.
✨Tip Number 2
Prepare for interviews by researching the company and its recent projects. Show us you’re genuinely interested in Novartis and how your expertise aligns with their goals in Translational Medicine.
✨Tip Number 3
Practice your pitch! Be ready to explain how your background in FiH studies and Clinical Pharmacology makes you the perfect fit for the Associate Director role. Confidence is key!
✨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 take that extra step.
We think you need these skills to ace Associate Director, Translational Medicine Expert, TM Clinical Pharmacology
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter for the Associate Director role. Highlight your experience in Clinical Pharmacology and any relevant studies you've led. We want to see how your background aligns with our needs!
Showcase Your Expertise: Don’t hold back on sharing your knowledge! Include specific examples of your contributions to FiH studies or regulatory submissions. This is your chance to shine and show us why you're the perfect fit for this role.
Be Clear and Concise: Keep your application straightforward and to the point. Use clear 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 submit your application directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, it shows us you’re serious about joining our team!
How to prepare for a job interview at Novartis Farmacéutica
✨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 you're not just familiar with the theory but have practical insights too.
✨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.
✨Understand the Company’s Vision
Familiarise yourself with Novartis' development pipeline and their approach to Clinical Pharmacology. Being able to articulate how your expertise aligns with their goals will set you apart and show that you're genuinely interested in contributing to their success.
✨Prepare Questions
Have a few thoughtful questions ready for your interviewers. This could be about their current projects, team dynamics, or future challenges in Clinical Pharmacology. It shows you're engaged and eager to understand how you can fit into their plans.