Clinical Trials Contracts Lead (FMV & Compliance)

Genmab; Princeton (NJ); Hybrid; USD 134,320 - 201,480; Full time

Benefits offered by this job

401(k) match

Health benefits

Parental leave

Dental & Vision

Commuter benefits

Wellness programs

Job summary

Genmab is seeking a Contract Manager to lead end-to-end management of Clinical Trial Agreements (CTAs) and FMV negotiations. You will act as primary contact for contract execution with clinical sites and ensure regulatory compliance across CTAs and budgets.

The role is hybrid with flexibility for occasional remote work and requires strong communication, negotiation, and cross-functional collaboration to keep trials on schedule and within scope.

Qualifications

• Bachelor's degree in a relevant field.
• 7+ years in biotech/pharma operations or R&D.
• Strong contract negotiation experience.
• Experience with site financial agreements and budgets.
• Familiarity with GCP, ICH, FDA/EMA guidelines (financial perspective).

Responsibilities

• Lead end-to-end management of CTAs including drafting, negotiating, and executing.
• Serve as primary contact for contract execution and site communications.
• Ensure legal and regulatory compliance of CTAs and site budgets.
• Maintain inspection-ready documentation and version control.
• Provide updates to clinical trial teams on status, risks, and timelines.
• Support risk mitigation to protect trial timelines and site engagement.

Skills

Contract negotiation

Site financial agreements

Communication skills

Cross-functional collaboration

Microsoft Office tools

Education

Bachelor's degree

Tools

Excel

Word

PowerPoint

Outlook

SaaS tools

Job description

Genmab is seeking a Contract Manager to lead end-to-end management of Clinical Trial Agreements (CTAs) and FMV negotiations. You will act as primary contact for contract execution with clinical sites and ensure regulatory compliance across CTAs and budgets.

The role is hybrid with flexibility for occasional remote work and requires strong communication, negotiation, and cross-functional collaboration to keep trials on schedule and within scope.