Clinical Development Medical Director
Novartis Barcelona
Experteer Overview
In this role you lead end-to-end renal clinical development programs across the RDC continuum, shaping strategy from early to registrational phases. You translate data into clear clinical and regulatory paths, working in a global matrix to ensure rigorous safety and benefit–risk decisions.You provide medical leadership for trial deliverables and regulatory documents, partnering with GTDs and regional teams. You drive cross-functional execution and stakeholder engagement to advance disease areas and therapeutic goals. This position offers an opportunity to influence patient outcomes through expert medical strategy and program oversight.
Compensaciones / Beneficios- Provide clinical leadership and strategic medical input for clinical deliverables in the program
- Lead development of clinical sections of trial and program-level regulatory documents
- Drive execution of the clinical program/trial in collaboration with global line functions, GTDs, and regional medical associates
- Support safety oversight for the molecule and contribute to Safety Management Team activities
- Contribute medical input into Clinical Development Plans (CDP), Integrated Development Plans (IDP), and Clinical Trial Protocol (CTP) reviews
- Act as medical expert in external/internal stakeholder engagements and decision boards
- Collaborate with BR to transition pre-PoC projects to DDP and with BD&L on target identification and due diligences
- Support internal leadership in scientific partnerships and cross-functional storytelling to advance the program
- MD or equivalent medical degree
- Clinical practice experience 4 years (including residency); board certification or eligibility in disease area preferred
- Minimum 10 years of experience in clinical research or drug development
- Experience in Phases I–IV in academic or industry settings
- Working knowledge of renal disease area and ability to interpret efficacy/safety data
- Proven ability to form effective scientific partnerships with stakeholders
- Working knowledge of GCP, trial design, statistics, and regulatory development processes
- Previous global people management experience preferred
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