Job Summary
The Associate/Clinical Development Medical Director (CDMD) is responsible for leading the planning and management of assigned clinical programs to support trials from an end-to-end clinical development perspective.
About the Role
* Providing clinical leadership and strategic medical input for all clinical results in assigned projects or sections of clinical programs.
* Leading development of RLI related clinical sections of trial and program level regulatory documents.
* Driving execution of programs and/or clinical trials in partnership with global line functions, Global Trial Directors, and regional/country medical associates.
* SUPPORTING overall safety of molecules for assigned sections and contributing to overall program safety reporting.
* Supporting Clinical Development Head by providing medical input into Clinical Development Plans, Integrated Development Plans, and Clinical Trial Protocol reviews.
* Contributing to publication strategy of RLI/RLT compounds from a scientific standpoint.
Role Requirements
* Nuclear medicine Physician/Medical Doctor.
* Sophisticated knowledge and clinical training in oncology PET; Clinical practice experience ≥ 5 years preferred.
* Experience in Clinical Trials with a PET component.
* Experience with Radioligand therapy.
* Demonstrated ability to establish effective scientific partnerships with key partners.
* Solid understanding of GCP, clinical trial design, statistics, regulatory and clinical development processes.
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.