Genae is an innovative services provider for the medical industries. The development and marketing of medical devices and therapies in today’s global marketplace is a highly regulated process with strict requirements from many competent authorities.
By channeling our expertise and know-how in the most appropriate format, genae aims at helping to improve healthcare worldwide by providing a broad range of professional services, information and partnering solutions.
Function: You take responsibility for the administration and monitoring of clinical research projects according to our Standard Operating Procedures, the ICH-GCP Guidelines and ISO 14155. You analyze and evaluate clinical data, ensure compliance with protocol and overall clinical objectives; identify, select, initiate and close-out appropriate investigational sites for clinical studies. You monitor the sites in order to ensure that studies are carried out according to the applicable regulations and guidelines. Regular international travel (50%) is required.
Profile: By preference, you have a (para-) medical or scientific degree (biology / pharmacy) and at least one year of clinical research experience including monitoring, or at least a minimum of two years experience in pharmaceutical data management or as a study coordinator. You are a detailed oriented professional with good negotiation, time management and people skills. You are at least fluent in English and by preference in more European languages.
Please apply with your CV and cover letter by the 'apply' button below.
| Education Backgrounds: |
Biomedical Science Healthcare Science |
| Specialties: |
(Bio) Chemistry Biomedical Engineering Clinical Trial/Research Pharmaceutics |
| Education Level: |
Undergraduate (Bachelors) Postgraduate (Masters) |
| Experience: |
2 - 5 years 5 - 10 Years |
| Languages spoken: |
English |
| Job Location: | Antwerp, Belgium |
Type: Job
Deadline: 29th November 2013
Job reference (ID): 6372
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