Job Overview

Se pueden requerir diversas habilidades interpersonales y experiencia para el siguiente puesto. Por favor, asegúrese de consultar la descripción a continuación con atención.

At Genmab, we are dedicated to building extra[not]ordinary® futures together by developing antibody products and groundbreaking KYSO antibody medicines® that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a integral 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.

Key Accountabilities

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- 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 Agreements (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 contribute 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

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- 7+ years of experience in relevant operations and/or R&D; functions, the biotechnology/pharmaceutical, CRO or healthcare industry.

- Bachelor's degree required.

- 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 and written communication and negotiating skills.

- Advanced skills in Microsoft Office applications (Excel, Word, PowerPoint, Outlook) and SaaS‑based platform tools and other industry standard programs.

Attributes of a Successful Candidate

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- Self‑starter; motivated by working in a fast‑paced, ambiguous environment.

- Detail oriented, timeline driven and able to work in a structured environment as an individual and team contributor.

Compensation

The proposed gross annual base salary range for this position, in the primary location, based on a full‑time schedule is:

DKK 687,888.00 — 1,031,832.00

The final salary offer will depend on several factors, including your skills, qualifications and experience. In addition to base salary, this position is eligible for additional forms of compensation, such as discretionary bonuses and long‑term incentives.

Benefits

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- Pension

- Health insurance and wellness benefits

- Paid time off

- Employee support programs

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 an international presence across North America, Europe and Asia Pacific. xcskxlj For more information, please visit 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 ( ).

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📌 Senior Manager, Contract Management (Madrid)
🏢 Genmab
📍 Madrid