International Clinical Trial Managers (ICTMs)

As ICTM you will lead clinical trials on a fully human antibody used to treat immunological diseases and 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.

Project management with many contacts

You are responsible for the planning, initiation and conduct of a clinical trial. This includes leading a clinical team of specialists from Regulatory Affairs, Biometrics, Drug Supply, Safety and Medical Reporting. In addition, you are actively involved in selecting doctors and CROs for your study. Another key task is to ensure preparation of various documents such as protocols, CRFs and patient information.

 

Reporting to the Associate Director for Clinical Development, you take part in preparing and following up on the clinical trial budget for which you are responsible. You also participate in the development of new clinical operational processes across Genmab’s projects.

Experience with international trials 

You hold a relevant degree and have worked in the pharmaceutical industry or in a CRO. This has given you solid experience with international clinical trials. Your pro-active nature and structural and interpersonal skills enable you to motivate and lead a clinical team. Combined with your talent for coordination and communication this helps you reach ambitious goals. You are used to working with MS Office programs and are proficient in English – verbal as well as written.

Application and contact

Please mark your application “International Clinical Trial Manager” and send it to Genmab A/S, Toldbodgade 33, PO Box 9068, DK-1253 Copenhagen K or to job@genmab.com. Please indicate in your application, if you have any preferences regarding clinical area. For further information regarding the positions please contact HR Manager Ida Grønborg at +45 7020 2728.