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!

REQUIREMENTS

• Bachelor’s or Master’s degree in relevant technical area.
• Minimum requirement: 3-5 years in clinical trial operations.
• Experience in coordination and support activities for clinical trial conduct.
• Experience maintaining and tracking critical documentation.
• Excellent relational and communication skills in English.

THE ROLE

As Senior Clinical Trial Associate (Sr CTA) you play a key role in supporting Clinical Trial Team (CTT) and ensuring smooth trial operations. The Sr CTA assists with study documentation, regulatory compliance, communication between stakeholders, and overall trial coordination. This position is essential for maintaining high-quality clinical trial execution while ensuring adherence to Good Clinical Practice (GCP) guidelines and regulatory requirements. Our Sr CTA’s are expected to become Subject Matter Experts (SMEs) for assigned processes and systems.
The primary location for this role is Utrecht, The Netherlands. Candidates located in Denmark or the US are also welcome to apply.

RESPONSIBILITIES

eTMF Management:

• Setup, maintain, oversee and close the Sponsor eTMF across trial, country and sites levels.
• Manage TMF health (completeness, quality and timeliness), including the monitoring of milestones relevant for the respective trial and the upload of documents as needed, etc.
• Ensure Audit/Inspection readiness by conducting regular eTMF health checks, including monthly eTMF reviews, bi-annual eTMF spot-checks, and milestone completion oversight, etc.
• Oversee and collaborate with the CRO on eTMF responsibilities (filing and TMF Health)
• Assist during Audits and Inspections in trial related tasks as required

Meeting and Communication Management:

• Schedule and coordinate meetings, taking minutes and following up on action items (meeting schedule and recording, meeting minutes preparation, meeting material filing in the eTMF, etc.)
• Coordinate logistics for key CTT meetings
• Participate in regular eTMF calls with the CRO TMF Lead to monitor eTMF status and follow up on open actions
• If applicable, provide Clinical Trial Governance (CT Gov.) site and status updates

Plans and Resource Management:

• Organize and track clinical trial documentation and reports
• Assist in preparation of reports, presentations, and study-related materials
• Develop and maintain the study TMF Plan

Clinical Study Report (CSR) Management:

• Support filing appendices of Clinical Study Report (CSR)

Sr. CTA specific responsibilities:

• Assume increased autonomy and responsibility for all assigned tasks
• Develop into a SME for assigned processes and systems.
• Assist in the development and editing of Sponsor materials (SOPs and Work Instructions (WI)