Clinical Trial Manager

Genmab; Utrecht; On-site; EUR 119,120 - 178,680; Full time

Benefits offered by this job

401(k) plan

Health benefits

Paid time off

Tuition reimbursement

Job summary

A leading biotechnology company in Utrecht is seeking a Clinical Trial Manager to support the planning and execution of global clinical trials. You will oversee documentation, collaborate with stakeholders, and ensure compliance with quality standards. Ideal candidates have over 5 years of experience in clinical trial management and a solid grasp of ICH/GCP regulations. This position emphasizes teamwork and communication skills within a dynamic environment.

Qualifications

• 5+ years of experience in clinical trial management in pharmaceuticals.
• Solid understanding of ICH/GCP regulations.
• Experience in global, multi-center trials.

Responsibilities

• Support planning and execution of global clinical trials.
• Maintain accurate documentation and participate in inspections.
• Collaborate with CROs for site management.

Skills

Clinical trial management

Project management

Communication

Collaboration

Interpersonal skills

Education

Bachelor's degree in life sciences

Master's degree preferred

Job description

Overview

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!

Key Responsibilities

• Support the planning, setup, and execution of global clinical trials, ensuring activities are delivered in accordance with timelines, quality standards, and regulatory requirements.
• Ensure trial oversight by maintaining accurate documentation and participating in inspection readiness activities.
• Collaborate with CROs and internal stakeholders to support site feasibility, selection, activation, and ongoing site management.
• Drive in the oversight of service providers, tracking deliverables, timelines, and quality to ensure alignment with study expectations.
• Support risk identification and mitigation activities, contributing to risk-based quality management throughout the trial lifecycle.
• Drive in managing protocol deviations and trial-level issues, ensuring proper documentation, follow-up, and escalation as needed.
• Support trial data review and performance tracking, contributing to reporting and identification of potential issues.
• Work collaboratively within a global, matrixed team environment, building strong relationships with internal teams, vendors, and investigators.

Qualifications

• Bachelor’s degree in life sciences or related field (Master’s degree preferred).
• 5+ 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.
• Experience managing global, multi-center trials and working in a complex, matrixed organization.
• Project management and service provider oversight skills.
• Good communication, collaboration, and interpersonal skills.
• Oncology and/or therapeutic area–specific experience is highly desirable.

Compensation and Benefits

For US based candidates, the proposed salary band for this position is as follows: $119,120.00---$178,680.00. 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.

Culture and Wellness

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

About You

• You are genuinely passionate about our purpose
• You bring precision and excellence to all that you do
• You believe in our rooted-in-science approach to problem-solving
• You are a generous collaborator who can work in teams with a broad spectrum of backgrounds
• You take pride in enabling the best work of others on the team
• You can grapple with the unknown and be innovative
• You have experience working in a fast-growing, dynamic company (or a strong desire to)
• You work hard and are not afraid to have a little fun while you do so!

Locations

Genmab maximizes the efficiency of an agile working environment, when possible, for the betterment of employee work-life balance. Our offices are crafted as open, community-based spaces that work to connect employees while being immersed in our powerful laboratories. Whether you’re in one of our office spaces or working remotely, we thrive on connecting with each other to innovate.

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.