Senior Clinical Trial Manager

About the Role

At Genmab, we’re dedicated to developing and delivering innovative antibody-based therapeutics to improve the lives of patients. As a Senior Clinical Trial Manager (CTM), you will play a pivotal role in driving the success of our clinical trials through strategic oversight, operational excellence, and cross-functional collaboration. The Senior CTM partners closely with Clinical Trial Teams (CTTs), service providers, and investigators to ensure that our clinical studies are executed on time, within budget, and in full compliance with regulatory standards and Genmab’s high-quality expectations. This role offers the opportunity to work in a dynamic, global, and matrixed environment where you will be empowered to take ownership and lead with autonomy.

Responsibilities

• Lead the operational planning, setup, and execution of global clinical trials, ensuring delivery on time, and in compliance with regulatory and quality standards.
• Oversee trial documentation and systems, ensuring accuracy, completeness, and continuous inspection readiness.
• Drive site feasibility, selection, and activation strategies in collaboration with CROs and internal stakeholders.
• Manage and oversee CROs and other service providers, ensuring high-quality deliverables, adherence to timelines, and effective collaboration.
• Proactively identify, assess, and mitigate operational risks using risk-based quality management approaches.
• Oversee protocol deviations, issue management, and ensure appropriate escalation and resolution of trial-level challenges.
• Monitor trial performance and data quality, leveraging key metrics to drive decision-making and continuous improvement.
• Act as a key cross-functional leader, fostering strong collaboration across internal teams, vendors, and investigators.

Qualifications

• Bachelor’s degree in life sciences or related field (Master’s degree preferred).
• 8+ years of experience in clinical trial management within the pharmaceutical or biotechnology industry.
• Solid understanding of ICH/GCP regulations and the clinical drug development lifecycle.
• Proven experience managing global, multi-center trials and working in a complex, matrixed organization.
• Strong project management and service provider oversight skills.
• Excellent communication, collaboration, and interpersonal skills.
• Oncology and/or therapeutic area–specific experience is highly desirable.
• Ability to lead without authority and mentor others in a cross-functional environment.

Pay

For US-based candidates, the proposed salary band for this position is $130,720.00–$196,080.00. The actual salary offer will carefully consider a wide range of factors, including your skills, qualifications, experience, and location. Certain positions are eligible for additional forms of compensation, such as discretionary bonuses and long-term incentives.

Benefits

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.