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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 groundbreaking therapeutic breakthroughs.
- Benefits: Enjoy a diverse and inclusive work environment with 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: Be part of a mission-driven team committed to reimagining medicine.
The predicted salary is between 72000 - 108000 £ per year.
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.
About the Role
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!
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.
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Medical Director, Clinical Pharmacology employer: Novartis Farmacéutica
Contact Detail:
Novartis Farmacéutica 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 advancements in Clinical Pharmacology and First-in-Human studies. This knowledge will not only help you during interviews but also demonstrate your commitment to staying updated in this rapidly evolving field.
✨Tip Number 2
Network with professionals in the industry, especially those who have experience in clinical trials or work at Novartis. Engaging with them can provide valuable insights into the company culture and expectations for the Medical Director role.
✨Tip Number 3
Prepare to discuss your previous experiences with drug submissions and clinical study management. Highlight specific examples where your leadership made a significant impact on study outcomes, as this aligns closely with the responsibilities of the role.
✨Tip Number 4
Showcase your ability to collaborate effectively with cross-functional teams. The role requires strong communication skills and the ability to liaise with various stakeholders, so be ready to share examples of successful collaborations from your past.
We think you need these skills to ace Medical Director, Clinical Pharmacology
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and requirements of the Medical Director, Clinical Pharmacology position. Familiarize yourself with Novartis' mission and how this role contributes to their goals.
Tailor Your CV: Customize your CV to highlight relevant clinical study experience, particularly in Clinical Pharmacology and First-in-Human studies. Emphasize any leadership roles and your contributions to drug submissions or publications.
Craft a Compelling Cover Letter: Write a cover letter that showcases your medical degree, PhD/post-doctoral qualifications, and specific experiences that align with the job description. Mention your commitment to improving patient outcomes and how you can contribute to Novartis' vision.
Highlight Collaborative Experience: In your application, emphasize your ability to work collaboratively with cross-functional teams and external partners. Provide examples of how you've successfully managed relationships with CROs or other stakeholders in previous roles.
How to prepare for a job interview at Novartis Farmacéutica
✨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 First-in-Human studies.
✨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, as well as your ability to contribute to their ongoing projects.
✨Prepare for Cross-Functional Collaboration Questions
Since the role involves liaising with various teams and CROs, be ready to discuss your experience in cross-functional collaboration. Provide examples of how you've successfully worked with different stakeholders to achieve common goals in clinical research.
✨Emphasize Your Leadership Skills
As a Medical Director, you'll need strong leadership capabilities. Prepare to share instances where you've led teams or initiatives, particularly in clinical settings. Highlight your ability to guide projects while ensuring safety and compliance.
