Genmab
Clinical Trial Manager
DanmarkPosted 10 days ago
Full TimeMidDK
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Job Description
We are extra[not]ordinary *(ex· tra· not· or· di· nary |\ ik-ˈstr-not-ȯr-də-ˌner-ē) Adjective: A unique word for Genmab meaning to go way beyond what is usual; to be remarkable; proudly unique and aut
Key Highlights
- 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.
Qualifications
Required 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.
Skills & Technologies
GoGCP
About the Company
Genmab
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Job Details
Employment Type
Full Time
Experience Level
Mid
Location
Danmark
Posted
10 days ago
Country
DK