Clinical Development Medical Director - Oncology / Clinical Development Medical Directoress - Oncology
Novartis Pharma AG - June 8, 2025
Job ID
REQ-10050085
Date Posted: May 19, 2025
Location: Switzerland
Summary
The Clinical Development Medical Director (CDMD) serves as the global clinical leader for specific program-level activities and deliverables, including submission activities and clinical trials, under the guidance of the GPCH or Senior CDMD.
About the Role
This hybrid role can be based in Basel, Dublin, London, or Barcelona.
Major Accountabilities:
Provide clinical leadership and strategic medical insights for all clinical deliverables associated with assigned program activities, including individual protocols, clinical data review, regulatory documents, and publications.
Lead the development of clinical sections for regulatory documents, such as Investigator's Brochures, briefing books, and safety updates.
Drive execution of clinical program sections in collaboration with global line functions, Clinical Trial Heads (CTHs), and regional medical associates.
Offer medical oversight and leadership in trials, including acting as a medical monitor and contributing to final analyses and Clinical Study Reports (CSRs).
Support the GPCH or Senior CDMD in benefit/risk assessments and ongoing safety monitoring of the molecule, while contributing to program safety reporting.
Contribute medical input to Integrated Development Plans (IDP), Clinical Development Plans (CDP), and develop clinical standards for new disease areas.
As a medical expert, engage with external stakeholders such as regulatory authorities and key opinion leaders, and represent Novartis at steering committees for clinical trials.
Work with Biomedical Research/Translational Medical Sciences to facilitate the transition of projects to Development Decision Points (DDP) and collaborate with Business Development & Licensing (BD&L) on relevant medical matters.
Minimum Requirements:
MD or equivalent medical degree required, with advanced knowledge and clinical training in a relevant area preferred. Medical Board certification is advantageous; clinical practice experience of 4 years (including residency) is preferred.
A minimum of 5 years of experience in clinical research or global drug development, covering clinical activities across Phases I through IV; at least 3 years of hands-on involvement in conducting clinical trials in a global/matrix environment, preferably within the pharmaceutical industry.
Demonstrated scientific acumen and ability to analyze and interpret scientific literature and data.
Advanced knowledge of the assigned therapeutic area.
Proven ability to establish strong scientific partnerships with key stakeholders.
Why Novartis
At Novartis, helping individuals and their families affected by diseases involves more than just innovative science. It requires a community of dedicated and passionate professionals. Together, we collaborate, support, and inspire each other to create breakthroughs that transform patients' lives. Are you ready to join us in shaping a brighter future?
Application Process
Apply online using the form below. Please note that only applications matching the job profile will be considered.
Accessibility and Accommodation
Novartis is committed to providing reasonable accommodations to all individuals. If you require assistance during the recruitment process due to a medical condition or disability, please send an email to Show e-mailm"> with your contact information and details of your request. Don’t forget to include the job requisition number in your message.
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Location Options
Basel (City), Switzerland
Barcelona Gran Vía, Spain
Dublin (NOCC), Ireland
London (The Westworks), United Kingdom
Division
Development
Functional Area
Research & Development
Job Type
Full time
Employment Type
Regular
Shift Work
No
Novartis is dedicated to fostering an outstanding and inclusive work environment, where diverse teams reflect the communities and patients we serve.