Clinical Trial Administrator Medivir AB

Clinical Trial Administrator Medivir AB

Clinical Trial Administrator for Medivir AB

The company
Medivir develops innovative drugs with a focus on cancer where the unmet medical needs are high. The company is investing in indication areas where available therapies are limited or missing and there are great opportunities to offer significant improvements to patients. Collaborations and partnerships are important parts of Medivir's business model and the drug development as well as the commercialization is conducted either by Medivir or in partnership. Medivir's share (ticker: MVIR) is listed on Nasdaq Stockholm's Small Cap list. www.medivir.com.

Role description
Medivir are looking for a Clinical Trial Administrator who wants to be a part of an interesting development within the company. You enter an exciting development phase where a major investment will be in the company's projects in the cancer field. You will work both independently and in close cooperation in a cross-functional team with short decision paths and with great opportunity to influence. For the right person, there will be great opportunities in personal development in order to take on more responsibility and build a career within Medivir. The position is located at Medivir's office in Huddinge in newly renovated facilities.

Work assignments
Medivir is looking for an Administrator who has a background and experience in clinical study management. Part of the job is also to assist the Chief Medical Officer with for example travel reports, meeting organization and scheduling and planning of CMO’s calendar. Another task is to participate in the production of publications (coordinating, administrating and proofreading). You will 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.

Qualifications
Required:
  • Some years of experience as coordinator in the pharmaceutical industry or health care
  • GCP knowledge and experience from working with clinical trials
  • Good knowledge in Microsoft Office
  • Fluent spoken and written Swedish and English
Personal abilities:
  • To work independently but also be a genuine team player
  • Strong ability to structure and keep track of details
  • To cooperate in projects
For more information, please contact Lena Kredell Isaxon Senior recruitment consultant at Signpost, 0707 97 77 78
Mer info
Område Huddinge
Yrkesroll Administration, Koordinator, Hälsa & Sjukvård, Medicinsk forskning & Laboratorieverksamhet
Typ av anställning Heltid, Tillsvidareanställd
Rekrytering hanteras av Signpost
Sista ansökningsdag 11 apr (18 dagar kvar)