Expression of Interest: Medical Directors (MD)
Join to apply for the Expression of Interest: Medical Directors (MD) role at Novartis.
Summary
Are you ready to reimagine medicine and make a real impact on patients’ lives? At Novartis, we’re not just developing treatments—we’re transforming the future of healthcare. As a Medical Director, you’ll be at the forefront of clinical innovation, guiding breakthrough therapies from concept to reality. You’ll collaborate with world‑class scientists, clinicians, and cross‑functional teams to shape strategies that matter.
About the Role
Novartis is growing and we regularly have openings for Medical Director across our R&D function in London and Dublin.
Key Responsibilities
* Clinical Leadership: Provide strategic medical input and leadership for all clinical deliverables within assigned projects or clinical programs.
* Regulatory Documentation: Lead the development of clinical sections for trial and program‑level regulatory documents (e.g., protocols, investigator brochures, clinical study reports).
* Program Execution: Drive the execution of clinical trials in collaboration with global line functions, Global Trial Directors, and regional/country medical associates.
* Safety Oversight: Support the Global Program Clinical Head (GPCH) in ensuring the safety of the molecule, including participation in the Safety Management Team and collaboration with Patient Safety colleagues.
* Strategic Planning: Contribute to the Clinical Development Plan (CDP), Integrated Development Plan (IDP), and disease area clinical standards.
* Cross‑functional Collaboration: Act as a medical expert in interactions with internal stakeholders (e.g., Translational Medicine, Business Development & Licensing) and external partners.
* Innovation & Transition: Support the transition of pre‑proof‑of‑concept (PoC) projects to full development and contribute to target identification and due diligence processes.
Qualifications
* Education: MD or equivalent medical degree required.
* Experience:
o Clinical research or drug development.
o Clinical practice experience (4+ years including residency) preferred.
o Specialization and deep expertise in our core therapeutic areas including Radioligand therapy (RLT), Immunology, Rheumatology, Dermatology, Nephrology, Oncology, T‑Charge (CAR‑T).
* Skills:
o Strong understanding of GCP, clinical trial design, and regulatory processes.
o Proven ability to interpret and present clinical data.
o Effective communicator with experience in matrixed, global environments.
Benefits and Rewards
Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards
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? https://www.novartis.com/about/strategy/people-and-culture
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