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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 groundbreaking research.
- Benefits: Competitive salary, professional development, and a supportive community focused on collaboration.
- Other info: Be part of a dynamic team driving breakthroughs in healthcare.
- Why this job: Make a real impact in drug development and improve lives through your expertise.
- Qualifications: MD with PhD/post-doctoral training and significant experience in Clinical Pharmacology.
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.
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.
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).
- 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.
This role significantly influences the success of the Novartis development pipeline by:
- 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.
- 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).
- Strategy Development
- Project Management
- Collaborating across boundaries
- Operations Management and Execution
- Representing the organization
- Clinical Trials
- Cross-Functional Teams
- Data Analysis
- Data Monitoring
- Drug Development
- Drug Discovery
- Medical Research
- Medical Strategy
- People Management
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.
Director, Translational Medicine Expert, Clinical Pharmacology employer: Novartis
Contact Detail:
Novartis 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, attend relevant conferences, and engage with professionals on platforms like LinkedIn. We all know that sometimes it’s not just what you know, but who you know that can help you land that dream role.
✨Tip Number 2
Prepare for interviews by researching the company and its projects thoroughly. Understand their values and recent developments in Clinical Pharmacology. We want you to walk in feeling confident and ready to discuss how your expertise aligns with their goals.
✨Tip Number 3
Practice your pitch! Be ready to explain your experience and how it relates to the role of Director, Translational Medicine Expert. We suggest rehearsing with a friend or mentor to get comfortable with articulating your achievements and vision.
✨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 proactive about their job search. Let’s make this happen together!
We think you need these skills to ace Director, Translational Medicine Expert, 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 mission. Keep it engaging and personal – we love to see your personality come through.
Showcase Your Collaborative Spirit: Since this role involves working closely with cross-functional teams, make sure to highlight your teamwork skills. Share examples of successful collaborations and how they led to impactful outcomes in your previous roles.
Apply Through Our Website: We encourage you to apply directly through our website for a smoother application process. It’s the best way for us to receive your application and ensures you’re considered for the role you’re excited about!
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. This is your chance to show that you’re not just familiar with the concepts but can also apply them in real-world scenarios.
✨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 how it has positively impacted study outcomes.
✨Prepare for Collaboration Questions
Expect questions about how you work with others, especially with CROs and internal stakeholders. Think of specific instances where your collaboration led to successful project outcomes. This will show that you understand the importance of teamwork in achieving clinical goals.
✨Be Ready to Discuss Regulatory Insights
Since this role involves regulatory submissions, be prepared to talk about your experience with regulatory bodies and submission processes. Familiarise yourself with recent changes in regulations that could impact Clinical Pharmacology studies, as this will demonstrate your proactive approach to staying informed.