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Director, Medical Monitor

vor 4 Monaten

Zug, Schweiz Seagen Vollzeit

Position Summary:
Principal Responsibilities:

- Establish and drive teams to execute the strategic long-term vision for the program
- Lead clinical study teams and ensure appropriate medical monitoring for ongoing clinical studies
- Lead development and maintenance of clinical documents (e.g. protocols and amendments, investigator brochures, clinical study reports)
- Lead development of clinical study documents to be used in regulatory interactions and filings
- Develop manuscripts, abstracts and presentations for scientific meetings
- Advise on current and future clinical development plans within internal teams with representatives from development and commercial functions
- Evaluate safety, pharmacology, and efficacy data from ongoing and completed studies to inform clinical strategy
- Conduct literature reviews and prepare summaries to support clinical development strategies

Qualifications:

- Medical Doctor (M.D.) or non-US equivalent of M.D. degree with relevant therapeutic expertise in an academic or hospital environment. Board certification in internal medicine or oncology preferred.
- 3+ years of industry experience or 3+ years of clinical experience after oncology fellowship
- 1+ years' experience leading diverse teams
- Strong leadership presence and the ability to work effectively with other clinical and scientific leaders
- Demonstrates a passion for helping patients with cancer and for the science of oncology
- Collaborative style with internal company leadership and colleagues, as well as external collaborators, including investigators/medical professionals
- Team player, works well in a team environment both as a leader and a key contributor
- Global perspective and mindset, with the ability to work effectively with colleagues from myriad cultures, backgrounds and geographies
- #LI-LO1_