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- Tasks: Lead and manage First-in-Human and Clinical Pharmacology studies with excellence.
- Company: Join Novartis, a leader in innovative healthcare solutions.
- Benefits: Competitive salary, inclusive culture, and opportunities for professional growth.
- Why this job: Make a real impact on drug development and patient lives.
- Qualifications: Medical degree and significant experience in Clinical Pharmacology required.
- Other info: Hybrid role based in London with a commitment to 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 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 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.
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
- 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?
Skills Desired
- Clinical Trials
- Cross-Functional Teams
- Data Analysis
- Data Monitoring
- Drug Development
- Drug Discovery
- Medical Research
- Medical Strategy
- People Management
Director, Translational Medicine Expert, Clinical Pharmacology 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
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, especially those who work at Novartis or similar companies. A friendly chat can lead to insider info about job openings and even referrals.
✨Tip Number 2
Prepare for interviews by diving deep into the company’s projects and values. Show them you’re not just another candidate; you’re genuinely interested in their mission and how you can contribute to their success.
✨Tip Number 3
Practice your pitch! Be ready to explain how your experience aligns with the role of Director, Translational Medicine Expert. Highlight your leadership skills and any relevant studies you've managed.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you’re serious about joining the team at Novartis.
We think you need these skills to ace Director, Translational Medicine Expert, Clinical Pharmacology
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, and show us how you can contribute to our mission.
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.
Be Clear and Concise: We appreciate clarity! When writing your application, keep it straightforward and to the point. Use bullet points where necessary to make your achievements stand out and easy to read.
Apply Through Our Website: We encourage you to apply directly through our website. This way, you’ll ensure your application reaches us quickly and efficiently, and you’ll get all the latest updates on your application status!
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 is your chance to showcase 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 your ability to lead and manage multiple projects while ensuring everyone is aligned.
✨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. This will demonstrate your strategic thinking and operational excellence.
✨Align with Company Values
Familiarise yourself with Novartis' commitment to diversity and inclusion. Be prepared to discuss how you can contribute to creating an inclusive environment and how your values align with theirs. This shows you're not just a fit for the role, but for the company culture too.