Job ID: REQ-10029778
Date: May 19, 2025
Location: Switzerland
Summary
As the Clinical Development Medical Director in our Immunology Development Unit, you will be at the forefront of shaping the scientific and clinical strategy for assigned clinical trials, overseeing the rigorous monitoring and reporting of quality data.
About the Role
The Clinical Development Medical Director (CDMD) for Rheumatology serves as the clinical leader for defined program-level activities, including submission activities and briefing books, or may oversee a large, complex trial under the guidance of the (Sr.) GPCH. This role may also entail leading a specific section of a clinical program focused on an indication, a new formulation, or a particular development phase.
Your Responsibilities
- Provide clinical leadership and medical strategic insights for deliverables in the assigned project/program, which may include sections of individual protocols, data reviews, and various regulatory documents.
- Drive execution of the program section in collaboration with global line functions, assigned Global Trial Directors (GTDs), and regional medical associates.
- Oversee the medical and scientific review of trial data with Clinical Scientific Experts, potentially acting as the Program Manager for other associates.
- Support the (Sr.) GPCH in ensuring the overall safety of the molecule as a key member of the Safety Management Team (SMT).
- Assist the Therapeutic Area Head (TAH) with medical input into IDP and CTP reviews, contributing to the development of clinical standards.
- Facilitate interactions with external partners, such as regulatory authorities and patient advocacy groups, and internal partners.
- Collaborate with Novartis Institute of Biomedical Research (NIBR) to transition pre-PoC projects to DDP and aid in target identification and due diligence processes.
- Foster career development for Program reports and clinical colleagues through active participation in performance management and mentoring.
- Contribute to training for relevant Novartis stakeholders on disease areas and compounds/molecules.
- Lead or participate in global initiatives focused on process improvement and training.
Minimum Requirements
- MD (or equivalent medical degree) required; Medical Board certification preferred.
- 4+ years of clinical practice experience (including residency) preferred.
- Advanced knowledge in a medical/scientific area (e.g., internal medicine or sub-specialty) required.
- 5+ years of experience in clinical research or drug development in the pharma/biotech industry, particularly in phases I through IV.
- 3+ years of experience in all aspects of conducting clinical trials in a global/matrix environment.
- Proven knowledge of the assigned therapeutic area and ability to establish strong scientific partnerships.
- In-depth understanding of GCP, trial design, statistical analysis, and the regulatory/clinical development process.
- People management experience preferred, particularly in a matrix environment.
- Excellent business communication, presentation, and interpersonal skills.
- Strong negotiation and conflict resolution capabilities.
Novartis is an equal opportunities employer and welcomes applications from all suitably qualified candidates.
Application Process
This hybrid role can be based in Basel, London, Barcelona, Madrid, or Dublin.
Apply online using the form below.
Note: Only applications matching the job profile will be considered.
Why Novartis?
At Novartis, helping people with diseases and their families involves more than just innovative science; it requires a community of smart, passionate individuals ready to collaborate, support, and inspire each other. Together, we aim to achieve breakthroughs that can change patients' lives. Are you ready to help create a brighter future?
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Division
Development
Business Unit
Innovative Medicines
Location
Switzerland
Company / Legal Entity
Novartis Pharma AG