At a Glance
- Tasks: Lead and manage First-in-Human and Clinical Pharmacology studies with excellence.
- Company: Join a leading biotech firm dedicated to 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).
Associate Director, Translational Medicine Expert, TM Clinical Pharmacology employer: Novartis UK
As an Associate Director in Translational Medicine at our London office, you will join a dynamic and innovative team dedicated to advancing clinical pharmacology studies. We pride ourselves on fostering a collaborative work culture that prioritises employee growth through continuous learning opportunities and mentorship, while also offering competitive benefits and a commitment to participant safety and scientific excellence. Our strategic outsourcing model allows for impactful contributions to drug development, making this an exciting place for professionals seeking meaningful and rewarding careers.
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 brushing up on your knowledge of FiH studies and Clinical Pharmacology. We recommend practising common interview questions with a friend or mentor to boost your confidence.
✨Tip Number 3
Showcase your expertise! Bring along examples of your previous work, like study reports or publications, to demonstrate your contributions to drug development during interviews.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are genuinely interested in 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 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 Translational Medicine and how your expertise can contribute to our team. Keep it engaging and make sure to connect your skills to the job description.
Showcase Your Collaboration Skills:Since this role involves working closely with cross-functional teams, highlight any experiences where you’ve successfully collaborated with others. We love seeing examples of teamwork and how you’ve contributed to achieving common goals.
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 gives you a chance to explore more about what we do 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 is your chance to show off your expertise!
✨Showcase Collaboration Skills
Since this role involves working closely with cross-functional teams and CROs, prepare examples of how you've successfully collaborated in the past. Highlight any strategic initiatives you've led or contributed to that improved study outcomes.
✨Prepare for Scenario Questions
Expect questions that assess your problem-solving skills in real-world scenarios. Think about challenges you've faced in previous studies and how you overcame them. Use the STAR method (Situation, Task, Action, Result) to structure your answers.
✨Ask Insightful Questions
At the end of the interview, have a few thoughtful questions ready. Inquire about the company's approach to regulatory submissions or how they ensure participant safety in studies. This shows your genuine interest in the role and the organisation.
