At a Glance
- Tasks: Lead and manage First-in-Human and Clinical Pharmacology studies with excellence.
- Company: Join a leading biopharmaceutical company focused on innovative drug development.
- Benefits: Competitive salary, comprehensive health benefits, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on scientific excellence and career advancement.
- Why this job: Make a real impact in drug development and enhance patient safety.
- Qualifications: MD with PhD/post-doctoral training and significant experience in Clinical Pharmacology.
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
- 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).
Benefits and Rewards
Read our handbook (PDF 30 MB)
Associate Director, Translational Medicine Expert, TM Clinical Pharmacology in London employer: Novartis UK
As an Associate Director in Translational Medicine at our London office, you will thrive in a dynamic and collaborative work culture that prioritises innovation and scientific excellence. We offer competitive benefits, including opportunities for professional development and growth, while fostering a supportive environment that values your contributions to impactful clinical research. Join us to be part of a leading team that shapes the future of medicine through high-quality data and strategic partnerships.
StudySmarter Expert Advice🤫
We think this is how you could land Associate Director, Translational Medicine Expert, TM Clinical Pharmacology in London
✨Network Like a Pro
Get out there and connect with people in the industry! Attend conferences, webinars, or local meetups related to Clinical Pharmacology. You never know who might have a lead on your dream job or can introduce you to someone at Novartis.
✨Showcase Your Expertise
When you get the chance to chat with potential employers, make sure to highlight your experience in FiH studies and your contributions to drug development. Share specific examples of how you've driven projects forward—this will set you apart from the crowd!
✨Prepare for Interviews
Do your homework before interviews! Understand the latest trends in Clinical Pharmacology and be ready to discuss how your background aligns with their needs. Practise common interview questions and prepare some insightful questions to ask them too.
✨Apply Through Our Website
Don’t forget to apply directly through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you're genuinely interested in joining our team at Novartis.
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 reflects the specific skills and experiences that align with the Associate Director role. Highlight your expertise in Clinical Pharmacology and any relevant studies you've led or contributed to.
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about Translational Medicine and how your background makes you the perfect fit for our team. Don't forget to mention your experience with FiH studies!
Showcase Your Collaborative Spirit:Since this role involves working closely with cross-functional teams, make sure to highlight examples of successful collaborations in your application. We love seeing how you’ve partnered with others to achieve great results!
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands and shows us you’re serious about joining our team at StudySmarter!
How to prepare for a job interview at Novartis UK
✨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 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 ask how you would handle specific challenges in Clinical Pharmacology studies. Think about potential issues like participant safety or regulatory compliance and prepare structured responses that showcase your problem-solving abilities.
✨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 shows your genuine interest in the role and helps you assess if the company is the right fit for you.
