Clinical Research Expert for Solid Tumors

2 weeks ago


Copenhagen, Copenhagen, Denmark Genmab Full time

About the Role

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We are seeking a skilled Clinical Research Expert to join our Solid Tumors team. In this role, you will be responsible for leading or co-leading clinical trials in a therapeutic area for one or more compounds.

Your Key Responsibilities

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  • Develop and implement clinical trial strategies, working closely with cross-functional teams to ensure timely deliverables.
  • Collaborate with Medical Directors and other Clinical Research Scientists to achieve program goals.
  • Contribute to the development of clinical development plans, study protocols, and regulatory documents.
  • Provide medical input for country/site selection, feasibility assessment, and key opinion leader interaction.
  • Assist in training investigators, sites, and CRO/CRA as warranted.
  • Develop and review clinical and regulatory documents, including protocol, ICF, IB, annual safety updates, and study reports.
  • Participate in the development of case report forms and their completion guidelines.

About You

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  • You have a PhD, Pharm D, MS, or equivalent degree in a related discipline.
  • You possess minimum 6 years of experience in clinical research, with at least 3 years in drug development.
  • Prior oncology/hematology drug development experience is highly valued.
  • You demonstrate proven skills in project-oriented matrixed team environments.
  • Excellent oral, written, and interpersonal communication skills are essential.
  • You can travel as needed.


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