Are you serviceminded and want to support Medivir in Stockholm with administration in clinical trials? Send your application now!
You will get the opportunity to enter an exciting development phase where a major investment will be in the company´s projects in the cancer field. The opportunity to influence as well as taking on more responsibility and build a career within Medivir will be great!
Looking forward to your application!
As a Clinical Trial Administrator at Medivir in Stockholm you will be part of this interesting development and work both independently and in close cooperation in a cross-functional team with short decision paths. The position is located at Medivir´s office in Huddinge in newly renovated facilities.
Your work assignments as a Clinical Trial Administrator will be to:
- assist the Chief Medical Officer with for example travel reports, meeting organization and scheduling and planning of CMO´s calendar
- participate in the production of publications (coordinating, administrating and proofreading)
- cooperate in certain tasks with the CEO´s Executive Coordinator when needed
In this role you will be part of a team of five people and report directly to the Chief Medical Officer. The position is full-time as soon as we find the right candidate. The position is located at Medivir´s office in Huddinge, Stockholm.
We are looking for an Administrator who has a background and experience in clinical study management. You probably have some years of experience as a coordinator in the pharmaceutical industry or within health care. Having GCP (Good Clinical Practice) knowledge and experience from working with clinical trials is a requirement.
Your ability to work independently but also be a genuine team player is essential. The abililty to structure and keep track of details is higly important as you will handle a lot of important information. You will need to be fluent in spoken and written English as well as Swedish and have a good knowledge in Microsoft Office.