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For Companies At a Glance
- Tasks: Lead clinical pharmacology studies and provide medical expertise for innovative therapies.
- Company: Join Novartis, a leader in biomedical research focused on therapeutic breakthroughs.
- Benefits: Enjoy a diverse work environment, competitive rewards, and opportunities for professional growth.
- Why this job: Make a significant impact on drug development and improve patient lives through innovative research.
- Qualifications: Medical degree with PhD/post-doctoral training and experience in clinical pharmacology required.
- Other info: Full proficiency in English is essential; join a mission-driven team at Novartis.
The predicted salary is between 72000 - 108000 £ per year.
Job Description Summary
Novartis Biomedical Research (BR) is the innovation engine of Novartis, focusing on powerful new technologies that have the potential to help produce therapeutic breakthroughs for patients.
Translational Medicine (TM) is the clinical research arm of BR and includes about 900 associates globally. TM plays a pivotal role in bringing innovative medicines to patients, by building on research advances to develop new therapies, and bridging drug discovery and clinical application.
TM Clinical Pharmacology is a cross-functional team, which is specialized on the design, clinical execution and reporting of First-in-Human (FiH) and Clinical Pharmacology studies across all TM therapeutic areas. The operating model is built upon a strategic outsourcing partnership with qualified and specialized CROs, in which the Novartis team maintains sponsor oversight and retains the strategic elements of the studies (e.g. study design, regulatory interactions, project timelines).
As part of TM Clinical Pharmacology, you will help to develop therapies for patients, by providing medical and scientific leadership and expertise to support both early and late-stage global programs across all BR therapeutic areas in a role that significantly affects the entire Novartis drug development pipeline.
Job Description
The Medical Director, Clinical Pharmacology (MD CP) will be the primary point of contact for the cross-functional Clinical Pharmacology (CP) Trial Team and for our qualified CROs used in the Clinical Pharmacology Partnership Model for any safety-related, medical and clinical pharmacology-related questions.
The MD CP will liaise with the project level Translational Medicine Expert to familiarize with the compound background and program strategy to ensure adequate medical supervision and execution of the study in the best interest of the program and the safety of study participants.
The MD CP will also support the project teams with Clinical Pharmacology advice to ensure study designs are optimal to serve the program strategy.
Clinical Pharmacology portfolio
Efficient and autonomous management and Medical and Clinical Pharmacology leadership for multiple, simultaneously conducted FiH and Clinical Pharmacology studies, including:
- Contribution and provision of Clinical Pharmacology expertise for the development of Study Concept Sheets and Protocols
- Review of Informed Consent Forms, Statistical Analysis Plans, Tables, Listings and Figure (TLF) shells and drafts, and results summaries
- Medical and Clinical Pharmacology coverage for Site Initiation Visits, during the clinical conduct of the trial, for safety reviews and safety reporting and for medical coding
- Development of the Clinical Study Report and contribution to publications of study results, including abstracts, posters, manuscripts, plain language trial summaries and technical results summaries.
Clinical Pharmacology strategy and initiatives
Contribution to strategic initiatives and process optimization workstreams in TM Clinical Pharmacology, strengthening the collaboration with internal stakeholders in early and full development and external partners.
Impact of this role
This role has a significant impact on the entire Novartis pipeline, by supporting the efficient clinical execution of FiH and Clinical Pharmacology studies for early and full clinical development programs in accordance with the Clinical Development Plan and Clinical Pharmacology Plan, by enabling efficient and result-based decision-making and by delivering key study results to support regulatory submissions.
- As a recognized specialist in the field, your strong experience in early clinical development and Clinical Pharmacology will enrich the Medical Team’s expertise and will help to build and grow Clinical Pharmacology as the Novartis Center of Excellence for FIH and Clinical Pharmacology studies across all therapeutic areas in the BR portfolio.
- The Medical Director, Clinical Pharmacology, will further help to strengthen our collaboration with our internal Novartis stakeholders in early and full development and to establish efficient partnerships with our qualified CROs.
Minimum Requirements
- Medical Degree combined with a PhD/post-doctoral degree, specialized training (board certification) or clinical research experience in Clinical Pharmacology.
- Previous relevant & significant clinical study experience, across the broad spectrum of Clinical Pharmacology and FIH studies, either in the biopharmaceutical industry leading early phase clinical trials, as a PI or sub-investigator in a CRO or relevant academic medical center.
- Track record of drug submissions / approval and / or high-quality publications in international scientific journals and advanced training or additional clinical development experience in one of the TM Therapeutic areas would be an upside.
- Full professional proficiency in English (written and spoken).
Why Novartis?
Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us!
You’ll receive : You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook.
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.
Accessibility & Accommodation : Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network.
Skills Desired
Clinical Trials, Cross-Functional Teams, Data Analysis, Data Monitoring, Drug Development, Drug Discovery, Medical Research, Medical Strategy, People Management
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Medical Director, Clinical Pharmacology employer: Novartis
Contact Detail:
Novartis Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Medical Director, Clinical Pharmacology
✨Tip Number 1
Familiarize yourself with the latest trends and advancements in Clinical Pharmacology. This will not only enhance your knowledge but also demonstrate your commitment to the field during discussions with our team.
✨Tip Number 2
Network with professionals in the biopharmaceutical industry, especially those involved in early phase clinical trials. Building these connections can provide valuable insights and potentially lead to referrals.
✨Tip Number 3
Prepare to discuss your previous experiences with FiH studies and how they relate to the role. Highlight specific examples where you contributed to study designs or safety reviews, as this will resonate well with our expectations.
✨Tip Number 4
Stay updated on Novartis' recent projects and initiatives in Translational Medicine. Showing that you are informed about our work will help you stand out as a candidate who is genuinely interested in joining our mission.
We think you need these skills to ace Medical Director, Clinical Pharmacology
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Medical Director, Clinical Pharmacology position. Understand the key responsibilities and required qualifications to tailor your application accordingly.
Highlight Relevant Experience: In your CV and cover letter, emphasize your clinical study experience, particularly in Clinical Pharmacology and First-in-Human studies. Provide specific examples of your contributions to drug submissions or high-quality publications.
Showcase Leadership Skills: Since the role requires medical and scientific leadership, be sure to highlight any previous leadership roles or experiences where you successfully managed cross-functional teams or projects.
Tailor Your Application: Customize your cover letter to reflect your understanding of Novartis' mission and values. Explain how your background aligns with their goals in improving patient outcomes through innovative therapies.
How to prepare for a job interview at Novartis
✨Showcase Your Clinical Expertise
Make sure to highlight your extensive experience in clinical pharmacology and early-phase clinical trials. Be prepared to discuss specific studies you've led or contributed to, emphasizing your role in the design and execution of these trials.
✨Understand the Novartis Pipeline
Familiarize yourself with Novartis' drug development pipeline and recent therapeutic breakthroughs. This knowledge will demonstrate your genuine interest in the company and its mission to improve patient outcomes.
✨Prepare for Cross-Functional Collaboration Questions
Since this role involves liaising with various teams and CROs, be ready to discuss your experience working in cross-functional teams. Provide examples of how you've successfully collaborated with different stakeholders to achieve project goals.
✨Discuss Regulatory Knowledge
Given the importance of regulatory submissions in this role, be prepared to talk about your understanding of regulatory requirements and your experience with drug submissions or approvals. Highlight any relevant publications that showcase your expertise in this area.
