Clinical Trial Manager

Genmab; København; On-site; DKK 620,160 - 930,240; Full time

Benefits offered by this job

Pension

Health insurance and wellness benefits

Paid time off

Employee support programs

Job summary

Genmab in Copenhagen is seeking an experienced Clinical Trial Manager to support the planning and execution of global clinical trials. The ideal candidate will have over 5 years experience in clinical trial management and a strong understanding of ICH/GCP regulations.

The role involves collaborating with CROs and internal stakeholders to ensure trials meet timelines and quality standards. Benefits include a competitive salary, pension, health insurance, and paid time off.

Qualifications

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

Responsibilities

• Support planning and execution of global clinical trials.
• Ensure trial oversight and maintain accurate documentation.
• Collaborate with CROs for site management.

Skills

Clinical trial management

Project management

Good communication

Collaboration

Interpersonal skills

Education

Bachelor’s degree in life sciences

Master’s degree (preferred)

Job description

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 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.
• Oversee 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

Gross annual base salary range: DKK620,160.00—930,240.00.

Final offer will depend on skills, qualifications, and experience.

Additional compensation may include discretionary bonuses and long‑term incentives.

Benefits

• Pension
• Health insurance and wellness benefits
• Paid time off
• Employee support programs