Sr. Manager, Contract Management

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

At Genmab, we are dedicated to building extra[not]ordinary® futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines® that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals’ unique contributions are valued and drive innovative solutions to meet the needs of our patients, care partners, families and employees.

Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science. We believe that being proudly authentic and determined to be our best is essential to fulfilling our purpose. Yes, our work is incredibly serious and impactful, but we have big ambitions, bring a ton of care to pursuing them, and have a lot of fun while doing so.

Does this inspire you and feel like a fit? Then we would love to have you join us!

Position Summary

The Contract Manager leads the end-to-end management of Clinical Trial Agreements (CTAs), Fair Market Value (FMV) negotiations and payment processes. As the primary contact for clinical trial sites, the role ensures our site contracts meet legal and regulatory requirements, real-time metrics and proper document management. The position requires strong communication and follow-up skills that directly contribute to faster study start-up timelines and smooth trial execution.

This role is hybrid and offers flexibility to work away from the office for 20%–40% of a typical schedule. Employees may use this work schedule in increments of single days or multiple consecutive days, provided it does not exceed 40% within a 60-day period, and is approved by the hiring manager.

Key Accountabilities (including but not limited to)

• End-to-End Site Contract Management
  Lead and oversee the full lifecycle of Clinical Trial Agreements (CTAs), including drafting, reviewing, negotiating, FMV, executing, and maintaining contracts. Implement, when possible, Master Clinical Trial (MCTAs) and support CTA amendments (as applicable).

• Primary Contact for Contract Execution
  Act as the central point within Genmab and our sites for all matters related to CTA execution, storage and management.

• Legal and Regulatory Compliance
  Ensure all CTAs and final site budgets remain in alignment with current legal, regulatory, and compliance requirements. Collaborate with Legal and Compliance teams to integrate evolving requirements into contracts.

• Documentation and Record Management
  Maintain complete, accurate, and inspection-ready documentation of all site contracts, correspondence, and approvals in accordance with internal- and regulatory requirements, as well as audit/inspection expectations. Ensure timely updates and version control across documentation systems.

• Stakeholder Communication & Reporting
  Partner with internal stakeholders to ensure transparency. Provide clear and timely updates on site contract status to the clinical trial team. Proactively contributes to trial-related meetings, ensuring alignment on contract progress, risks, and timelines.

• Inspection Readiness & Trial Support
  Support the core trial team in ensuring all site-level documentation and contracts are audit- and inspection-ready. Contribute to risk mitigation and resolution of issues impacting trial timelines or site engagement.

Qualifications/Experience

• Bachelor's degree and 7+ years of direct industry experience required

• Experience in relevant operations and/or R&D functions, the biotechnology/ pharmaceutical, CRO, or healthcare industry

• Strong expertise in Contract negotiation and site financial agreements

• Substantial Experience in reviewing and negotiating relevant agreements

• Familiarity with GCP, ICH, and relevant FDA/EMA guidelines from a financial perspective

• Demonstrated ability to collaborate across functional teams and communicate effectively with clinical and financial stakeholders

• Excellent verbal/written communication and negotiating skills

Attributes of a successful candidate

• Self-starter; motivated by working in a fast-paced, ambiguous environment
• Detail oriented, timeline driven and ability to work in a structured environment as an individual and team contributor

Demonstrate advanced skills in Microsoft Office applications (Excel, Word, PowerPoint, Outlook), Saas based platform tools and other industry standard programs

For US based candidates, the proposed salary band for this position is as follows:

$134,320.00---$201,480.00

The actual salary offer will carefully consider a wide range of factors, including your skills, qualifications, experience, and location. Also, certain positions are eligible for additional forms of compensation, such as discretionary bonuses and long-term incentives.

When you join Genmab, you’re joining a culture that supports your physical, financial, social, and emotional wellness. Within the first year, regular full-time U.S. employees are eligible for:

• 401(k) Plan: 100% match on the first 6% of contributions
• Health Benefits: Two medical plan options (including HDHP with HSA), dental, and vision insurance
• Voluntary Plans: Critical illness, accident, and hospital indemnity insurance
• Time Off: Paid vacation, sick leave, holidays, and 12 weeks of discretionary paid parental leave
• Support Resources: Access to child and adult backup care, family support programs, financial wellness tools, and emotional well-being support
• Additional Perks: Commuter benefits, tuition reimbursement, and a Lifestyle Spending Account for wellness and personal expenses

Further details on eligibility for compensation and benefits based on role will be provided during the recruitment process.

About Genmab

Genmab is an international biotechnology company with a core purpose to improve the lives of patients through innovative and differentiated antibody therapeutics. For 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. By 2030, Genmab’s vision is to transform the lives of people with cancer and other serious diseases with Knock-Your-Socks-Off (KYSO®) antibody medicines.

Established in 1999, Genmab is headquartered in Copenhagen, Denmark with international presence across North America, Europe and Asia Pacific. For more information, please visit Genmab.com and follow us on LinkedIn and X.

Genmab is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with your application on our website Job Applicant Privacy Notice (genmab.com).

Please note that if you are applying for a position in the Netherlands, Genmab’s policy for all permanently budgeted hires in NL is initially to offer a fixed-term employment contract for a year, if the employee performs well and if the business conditions do not change, renewal for an indefinite term may be considered after the fixed-term employment contract.