Director, Vendor Mgmt, Global Clinical Operations

Location
Tarrytown, NY, United States
Posted
Sep 19, 2019
Ref
17379BR
Required Education
Bachelors Degree
Position Type
Full time
Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases.

Summary:

The Director of GCO (Global Clinical Operations) Vendor & Relationship Management will be responsible for ensuring that the relationship between GCO and its strategic vendors is running efficiently and productively. As a leader within the organization, they will be instrumental in the concept, design, growth and deliverables of clinical trial execution as it relates to external partnerships to assure the highest quality delivery of Clinical Programs, on time and within budget.

Responsibilities:

• Support oversight of clinical trial execution with external partners.

• Ensure appropriate documentation of partnerships is developed and maintained

• Act as operational lead for relationships with key CROs

• Responsible for coordinating Joint Operations Committees, Executive Steering Committees, and other Governance Committees on behalf of Regeneron with key CROs including agendas, minutes, follow-up on action items

• Focus across the portfolio in collaboration with Clinical Trial Management, Cost Management, Finance and Procurement to ensure the vendors are executing clinical trials within budget, on time, and of the highest quality, through cross-company and cross-partnership collaboration

• Develop and/or enhance key vendor performance scorecards. Address areas of concern and provide recommendations to mitigate against poor performance

• Identify and communicate clinical development risks and mitigation strategies as they relate to key vendors

• Partner with the organization to optimize cross-functional communication

• Act as a lead for process optimization between CRO partners and Regeneron

• Assess portfolio resource demand and shortfall/mitigations for current and potential future portfolio with key vendors.

• Support integration of Regeneron and CRO teams and process to enhance success of new collaborations

• Aid in new key vendor identification and selection

• May require up to 25% travel

Requirements:

Education

• BS- Advanced degree in science or equivalent combination of relevant educational and professional experience is required; prior research and / or clinical training is desired

Experience

• Minimum of 10 years of experience and success in a clinical project/ trial management role within another biotech/pharmaceutical company

• 5 years of experience managing CRO and other ancillary vendors

SKC, #LI-SC1

This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron's unwavering commitment to combining good science & good business.

To all agencies: Please, no phone calls or emails to any employee of Regeneron about this opening. All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place. In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid.

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.