genae is involved in the development and commercialization of medical devices, biologics and therapies that change medical practice. Our expertise helps you in obtaining predictable outcomes, on time, on budget.
You take responsibility for the administration and monitoring of clinical research projects according to our Standard Operating Procedures and the relevant regulations.
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. You act as mentor for junior staff members. Regular international travel is required.
About genae
genae’s mission is to improve health and quality of life by innovating and accelerating high quality research – with a zealous dedication to safety and ethics. As a specialized medical device CRO, genae is involved in the development and commercialization of investigational productsand therapies that change medical practice.
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Education Backgrounds: |
Healthcare Science |
Specialties: |
Clinical Trial/Research Consultancy Lab Analysis Life sciences Pharmaceutics |
Education Level: |
Postgraduate (Masters) Doctorate (PH.D) |
Experience: |
10 - 15 years 2 - 5 years 5 - 10 Years |
Languages spoken: |
English German |
Job Location: | Frankfurt am Main, Germany |
Type: Job
Deadline: 10th January 2017
Job reference (ID): 9284
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