Executive Medical Director leading clinical development of nephrology and cardiometabolic disease therapies at Lilly. Collaborating with global teams in a healthcare leader company to innovate healthcare solutions.
About the role
- Medical Director responsible for oncology clinical development at GSK, leading clinical trials and data generation for cancer treatments.
Responsibilities
- Report to the Executive Medical Director, Clinical Development Lead (CDL), Oncology Clinical Development
- Responsible for clinical research activities pertaining to advancing the development of GSK’s clinical portfolio
- Engage in medical dialogues with relevant scientific and medical leaders
- Lead clinical data generation activities
- Manage effective relationships with Key External Experts
- Support the growing oncology antibody drug conjugate (ADC) portfolio for the treatment of solid tumors
- Work across early to late-stage development and in partnership with a multi-disciplinary team of oncology drug developers
- Collaborate with physicians, scientists, regulatory professionals, biostatisticians, regulatory, executive staff and others in a complex matrix environment to develop and execute phase 1-3 interventional clinical trials
- Ensure high quality protocol development aligned with the Clinical Development Plan
- Use medical expertise to contribute to the end to end (protocol concept to final study report)
- Interpret and summarize study results consistent with objectives
- Oversee blinded review of data packages intended for IDMCs
- Participate in authoring of clinical study reports and regulatory documents
- Network extensively to develop long-term strategic partnerships with thought leaders
Requirements
- Medical degree from accredited medical school
- Completion of a clinical residency program
- Clinical experience in medical oncology, hematology, or gyn oncology
- Experience in clinical research and development
- Oncology clinical research and drug development experience focused on Gynecologic Cancer or Breast cancer (preferred)
- Experience in the pharmaceutical/biotechnology industry; clinical academic medicine or clinical medical practice settings in the field of oncology or gynecologic oncology (preferred)
- Regulatory experience to support registration and GCP principle
Benefits
- health care and other insurance benefits (for employee and family)
- retirement benefits
- paid holidays
- vacation
- paid caregiver/parental and medical leave
- annual bonus
- eligibility to participate in share based long term incentive program
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