Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries, and growing - we look for talented people to grow our business, advance our science and contribute to our unique culture.
Responsibilities will include, but are not limited to, the following:
Perform and manage all activities associated with the development of clinical site contracts from study concept through to final protocol. Deliver clinical site agreements that protect Celgene business interests and compliance with regulations and laws concerning the same including compliance with Fair Market Value (“FMV”).
1. Support Global Project Teams during protocol development by:
2. Take a lead role within the Global Study Teams through:
3. Oversee and project manage all outsourced activities for clinical site contracts strategy and execution:
4. Working with peers and stakeholders:
5. Involved in projects or programs (complex and multiple)
Skills/Knowledge Required: