Hybrid Senior Contract Manager, Clinical Trials

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

Benefits offered by this job

401(k) match

Health benefits

Parental leave

Wellness programs

Tuition reimbursement

Commuter benefits

Job summary

Genmab is seeking a Contract Manager to lead end-to-end management of Clinical Trial Agreements (CTAs), FMV negotiations, and payment processes. You will be the primary contact for clinical trial sites, ensuring CTAs meet regulatory requirements and that documentation is complete and audit-ready.

This hybrid role allows 20%–40% remote work. The position requires 7+ years in biotech/pharma contract operations, strong negotiation and cross-functional collaboration, plus familiarity with GCP, ICH,

Qualifications

• Bachelor's degree required.
• 7+ years of direct industry experience.
• Experience in operations/R&D in biotech/pharma/healthcare.
• Strong contract negotiation and site financials expertise.
• Familiarity with GCP/ICH and FDA/EMA guidelines.
• Ability to collaborate across functional teams.

Responsibilities

• End-to-End Site Contract Management: manage CTAs from drafting to execution and maintenance.
• Primary contact for contract execution, storage, and management.
• Ensure CTAs and site budgets comply with legal, regulatory, and compliance requirements.
• Maintain audit-ready documentation and version control across systems.
• Communicate contract status and risks to clinical trial teams; participate in meetings.
• Support trial timelines and site engagement by mitigating risks.

Skills

Contract negotiation

Site financial agreements

Cross-functional collaboration

Communication skills

GCP/ICH/FDA/EMA knowledge

Education

Bachelor's degree

Tools

Microsoft Excel

Microsoft Word

PowerPoint

Outlook

SaaS platforms

Job description

Genmab is seeking a Contract Manager to lead end-to-end management of Clinical Trial Agreements (CTAs), FMV negotiations, and payment processes. You will be the primary contact for clinical trial sites, ensuring CTAs meet regulatory requirements and that documentation is complete and audit-ready.

This hybrid role allows 20%–40% remote work. The position requires 7+ years in biotech/pharma contract operations, strong negotiation and cross-functional collaboration, plus familiarity with GCP, ICH,