Associate Director, Vendor and Relationship Management

Location
Tarrytown, NY, United States
Posted
Oct 26, 2020
Ref
19914BR
Required Education
Bachelors Degree
Position Type
Full time
The Associate Director of Global Clinical Operations, Vendor & Relationship Management will be responsible for ensuring that a cohort of GCO and strategic vendor relationships are running efficiently and productively. We are looking for a leader to be instrumental in the concept, design, growth and outcomes of clinical trials as related to external partnerships. You will assure the highest quality delivery of Clinical Programs, on time and within budget.

As Associate Director, GCO, V&RM a typical day might include the following:
  • Supporting oversight of clinical trial execution with external partners.
  • Ensuring appropriate documentation of partnerships is developed and maintained
  • Acting as operational lead for relationships with key CROs
  • Coordinating Joint Operations Committees, Executive Steering Committees, and other Governance Committees on behalf of Regeneron with CROs including agendas, minutes, follow-up on action items
  • Developing and improving key vendor performance scorecards. Addressing areas of concern and providing recommendations to mitigate against poor performance
  • Assessing portfolio resource demand and shortfall/mitigations for current and potential future portfolio with key vendors.
  • Supporting integration of Regeneron and CRO teams and process to drive success of new collaborations
This role may be for you if you have:
  • Experience across clinical portfolios, collaborating with Clinical Trial Management, Cost Management, Finance and Procurement functions.
  • Extensive oversight experience, ensuring vendors are executing clinical trials within budget, on time, and of the highest quality
  • Expertise in cross-company and cross-partnership collaboration
To be considered for this opportunity you must have:

An advanced degree in science or equivalent combination of relevant educational and professional experience. Prior research and/or clinical training is desired. At least ten years in a clinical project/trial management role within the biotech/pharmaceutical industry. At least three years managing CROs and other ancillary vendors. Willingness to travel up to 25%.

Does this sound like you? Apply now to take your first steps toward living the Regeneron Way! We have an inclusive and diverse culture that provides amazing benefits including health and wellness programs, fitness centers and stock for employees at all levels!

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or maternity status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. We will ensure that individuals with disabilities are provided reasonable accommodations to participate in the job application process. Please contact us to discuss any accommodations you think you may need.
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