Clinical Trial Manager

Genmab • Plainsboro Township, NJ

8d

About The Position

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 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.

Nice To Haves

• Oncology and/or therapeutic area–specific experience is highly desirable.

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.

Benefits

• 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

What This Job Offers

• Job Type: Full-time
• Career Level: Manager
• Number of Employees: 501-1,000 employees