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- Tasks: Lead and manage innovative Clinical Pharmacology studies to shape drug development.
- Company: Join Novartis, a diverse and inclusive leader in the pharmaceutical industry.
- Benefits: Enjoy competitive rewards, professional growth, and a supportive community.
- Other info: Be part of a passionate team driving scientific breakthroughs.
- Why this job: Make a real impact on patient lives through groundbreaking research and collaboration.
- Qualifications: Medical degree with significant experience in Clinical Pharmacology studies.
The predicted salary is between 80000 - 100000 ÂŁ per year.
This job is with Novartis, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community.
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.
Location: London
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).
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients' lives. Ready to create a brighter future together?
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
Contact Detail:
Novartis 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. 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 FiH studies and Clinical Pharmacology. We recommend practising common interview questions and having examples ready that showcase your expertise and experience.
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, send a thank-you email to express your appreciation and reiterate your interest in the role. It keeps you fresh in their minds!
✨Tip Number 4
Apply through our website for the best chance at landing that Associate Director role. We keep track of applications better this way, and it shows you're serious about joining our team!
We think you need these skills to ace Associate Director, Translational Medicine Expert, TM Clinical Pharmacology
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the role of Associate Director, Translational Medicine Expert. Highlight your relevant experience in Clinical Pharmacology and any leadership roles you've held. We want to see how your background aligns with the job description!
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 skills can contribute to Novartis. We love seeing genuine enthusiasm, so let your personality come through!
Showcase Your Achievements: When detailing your experience, focus on specific achievements that demonstrate your impact in previous roles. Whether it's successful studies or innovative strategies, we want to know how you've made a difference in Clinical Pharmacology.
Apply Through Our Website: Don't forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re serious about joining our team at Novartis!
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 at Novartis. This shows you're not just familiar with the field but also passionate about it.
✨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 Culture
Novartis values inclusivity and collaboration. Familiarise yourself with their mission and values, and think about how your personal values align with theirs. This will help you convey that you're a good cultural fit during the interview.
✨Prepare Thoughtful Questions
Interviews are a two-way street! Prepare insightful questions about the role, team dynamics, and future projects. This not only shows your interest but also helps you gauge if Novartis is the right place for you.