Lead Clinical Research Associates

As Lead CRA you will assist our International Clinical Trial Managers (ICTM) in conducting a clinical trial with a fully human antibody to be used in the treatment of specific types of cancer. Genmab is currently moving into an exciting business development period, resulting in new challenges within all areas and offering you responsibilities and development opportunities that go beyond your specialist function.

International clinical studies

From our head office in Copenhagen you will assist the ICTM in managing a clinical study from initiation to completion. Specifically, you will provide input to and participate in a variety of clinical study activities such as feasibility studies, site selection and submission of applications to ethical committees. You will also prepare and maintain various documents, including patient information, manuals and guidelines for field CRAs and the participating study centers.

Another key task is to communicate with, train and assist the field CRAs in the participating countries, ensuring that they all work according to the established procedures and guidelines.

Experience with monitoring clinical studies 

You hold a relevant degree, but most importantly, you have experience with monitoring and/or participating in clinical studies from your previous positions in the pharmaceutical industry, CROs or at a hospital. Your pro-active and communicative nature combined with your structural and strong interpersonal skills enable you to coordinate and drive processes across departments. You are an experienced user of most MS Office programs and proficient in English.

Application and contact

Please mark your application “Lead Clinical Research Associate” and send it to Genmab A/S, Toldbodgade 33, PO Box 9068, DK-1253 Copenhagen K or to job@genmab.com. For further information regarding the position, please contact Associate Director, Clinical Development, Mimi Flensburg or HR Manager Ida Grønborg at +45 7020 2728.