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- Tasks: Lead and manage innovative Clinical Pharmacology studies, ensuring participant safety and scientific excellence.
- Company: Join Novartis, a leader in transforming patient care through cutting-edge research.
- Benefits: Competitive salary, inclusive culture, and opportunities for professional growth.
- Why this job: Make a real impact on drug development and improve lives through your expertise.
- Qualifications: MD with PhD/post-doctoral training and significant experience in Clinical Pharmacology.
- Other info: Collaborative environment focused on diversity and inclusion.
The predicted salary is between 100000 - 150000 £ per year.
As a Director, Translational Medicine Expert (TME), Clinical Pharmacology (CP TME), you will serve as the primary medical and scientific leader for First-in-Human (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.
TM Clinical Pharmacology is a cross-functional expert group responsible for the design, execution, and reporting of 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.
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.
Your 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.
Minimum 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).
Commitment to Diversity and Inclusion
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
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?
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Director, Translational Medicine Expert, Clinical Pharmacology in London employer: Healthcare Businesswomen’s Association
Contact Detail:
Healthcare Businesswomen’s Association Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Director, Translational Medicine Expert, 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 lead to opportunities that aren’t even advertised yet.
✨Tip Number 2
Prepare for interviews by researching the company and its recent projects. Show them you’re not just another candidate; you’re genuinely interested in their work and how you can contribute to their success.
✨Tip Number 3
Practice your pitch! Be ready to explain your experience and how it aligns with the role of Director, Translational Medicine Expert. Confidence is key, so rehearse until it feels natural.
✨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 take the initiative to connect directly with us.
We think you need these skills to ace Director, Translational Medicine Expert, Clinical Pharmacology in London
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter for the Director, Translational Medicine Expert role. Highlight your relevant experience in Clinical Pharmacology and FiH studies, as this will show us you’re the right fit for the job.
Showcase Your Leadership Skills: As a TME, you'll be leading teams and projects. Use your application to demonstrate your leadership experience and how you've successfully managed cross-functional collaborations in the past. We want to see how you can drive excellence!
Be Clear and Concise: When writing your application, keep it clear and to the point. Use bullet points where possible to make it easy for us to read through your achievements and qualifications. We appreciate straightforward communication!
Apply Through Our Website: Don’t forget to submit your application through our official website. This ensures that we receive all your details correctly and helps us keep track of your application. We can’t wait to hear from you!
How to prepare for a job interview at Healthcare Businesswomen’s Association
✨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 field but also passionate about it.
✨Showcase Your Leadership Skills
As a Director, you'll need to demonstrate your ability to lead cross-functional teams. Prepare examples of how you've successfully managed projects or teams in the past, particularly in high-pressure situations. Highlight your strategic thinking and decision-making skills.
✨Understand the Company Culture
Familiarise yourself with Novartis' commitment to diversity and inclusion. Be prepared to discuss how you can contribute to this culture and why it's important to you. This will show that you align with their values and are a good fit for the team.
✨Prepare Questions
Have thoughtful questions ready for your interviewers. Ask about their current projects, challenges they face in Clinical Pharmacology, or how they measure success in this role. This not only shows your interest but also helps you gauge if the company is the right fit for you.