Manager, Site Contracting

The Manager, Site Contracting is responsible for (1) managing the CROs who develop and negotiate global investigator site contracts, (2) reviewing CROs’ and/or sites’ proposed changes to standard contract terms and the study-specific budget parameters (in partnership with other business lines internally), (3) ensuring the delivery of high quality, compliant, effective, and timely site contracts, (4) maintaining productive relationships with internal client groups, (5) leading ongoing process improvements (including participating on critical initiatives), and (6) onboarding, training, and mentoring peers.

• Provide subject matter expertise for assigned therapeutic areas

• Accountable for ensuring that performance and efficiency standards are met for assigned studies

• Perform in a manger that is consistent with Regeneron’s values

• Assist with updating Regeneron’s site contracting processes

• Engage with the study teams from early planning throughout the end-to-end contracting lifecycle

• Work closely with internal client groups, internal partners, and CROs and effectively communicate with them, in order to ensure that business objectives are met (e.g., scheduled site initiation visit deadlines)

• Handle site contracting related escalations from the CROs and/or the investigator sites, effectively and efficiently

• Develop and enhance relationships with internal clients, internal partners, CROs, and sites

• Partner with colleagues in the Law Department and other partner groups, as needed, to continuously enhance Regeneron’s CTAs

• Ensure that internal systems are updated in a timely, accurate, and complete manner

• Ensure that CROs and staff are enhancing site relationships and conducting issue resolution of moderate to high complexity

• Meet with study teams regularly and prioritize assignments

• Stay abreast of changes in industry standards and help identify new best practices to contribute to continuous improvement

• Help train others on site contracting processes and industry practices

• Manage changes to study scope, ensuring timely contract amendment and implementation

• Responsible for making timely decisions and direction of outcomes

• Address changes to study scope to ensure timely contract amendment and implementation

• As a member of cross-functional study teams, lead appropriate agenda topics of the team meeting and provide guidance to line functions

• Lead ongoing, process improvements (including participating on strategic initiatives) and develop guidance documents

• Onboard, train, and mentor peers

• Single point of contact for internal clients, CROs, and sites for assigned studies

• May require up to 25% travel

Bachelor's degree required, Masters or Juris Doctor preferred.

• Minimum of 5 years of direct experience with clinical site contracting at a biopharmaceutical company, CRO, or site

• Minimum of 1 year of applicable people management and training experience

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.