Regulatory Affairs Jobs in Germany
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Global Medical Advisor-Diabetes Germany Permanent
- Salary:
- Excellent + Benefits
- Location:
- Germany
- Job Type:
- Permanent
- Date Posted:
- 06-Feb-2012 10:40Add to My Shortlist
Global Medical Advisor-Diabetes Germany Permanent A fast-growing top twenty pharma company is seeking a candidate to fill a post as as a global medical director in the specialism of diabetes. The role requires provision of medical expertise to medical and marketing professionals in the area of diabetic disease. The role demands interaction with regulatory and drug safety departments in developing...
Senior Drug Safety Physician (Germany)
- Salary:
- Negotiable
- Location:
- Germany
- Job Type:
- Permanent
- Date Posted:
- 10-Feb-2012 00:00Add to My Shortlist
A brilliant opportunity has arisen for a German speaking pharmacovigilance Medic within a top Biopharmaceutical company. The Senior Drug Safety Physician will play a crucial role in ensuring the successful release of products to market. You will be responsible for all safety assessments throughout the lifecycle of the product and your team will rely on you to ensure regulatory affairs...
Regulatory Affairs Specialist
- Salary:
- On Application
- Location:
- Berlin, Germany
- Job Type:
- Any
- Date Posted:
- 06-Feb-2012 16:02Add to My Shortlist
An opportunity has arisen to work in the Regulatory Department of one of the top 5 largest Pharmaceutical companies in the world and the largest in emerging markets. The client is looking for a Regulatory Affairs Specialist to work office based in Berlin. You will have experience in Post Marketing Regulatory Affairs and be sued to and comfortable working on...
Technical Writer ( JAVA / XML / DocBook ) - Cologne Germany
- Salary:
- Excellent Package
- Location:
- Koln , Koln , Germany
- Job Type:
- Permanent
- Date Posted:
- 10-Feb-2012 16:52Add to My Shortlist
Aptiv Solutions are a full service CRO and the only provider to offer the design, simulation and execution of Adaptive Clinical Trials in partnership with SAS, the leader in business analytics. Aptiv Solutions recently launched The Integrated Technology Platform Aptiv Advantage, this platform consists of all software applications specifically designed for the conduct of adaptive clinical trials (ACT): EDC system, ...
Technical Writer ( JAVA / XML / DocBook ) - Koln / Cologne Germany
- Salary:
- Excellent Package
- Location:
- Koln , Koln , Germany
- Job Type:
- Permanent
- Date Posted:
- 05-Feb-2012 00:00Add to My Shortlist
Aptiv Solutions are a full service CRO and the only provider to offer the design, simulation and execution of Adaptive Clinical Trials in partnership with SAS, the leader in business analytics. We now have a Technical Writer opportunity at our offices in Koln / Cologne, Germany; the successful person will become the first Technical Writer to join Aptiv Solutions in...
Regulatory Submissions Manager - EU
- Salary:
- On Application
- Location:
- Poland, Europe, Krakow, Warsaw, Berlin, Germany, Slovakia, Slovenia, Estonia, Lithuania, Czech Republic, Bulgaria
- Job Type:
- Permanent
- Date Posted:
- 10-Feb-2012 16:49Add to My Shortlist
Regulatory Submissions Manager - Poland Job Summary: Regulatory Submissions Manager - Poland. This role requires the candidate to efficiently manage and successfully execute all aspects of global submissions according to Sponsor specifications. The role is based around the achieving of successful submissions from sites in accordance with regulations, requirements, and SOPs. Requirements: Regulatory Submissions Manager - Poland * Assist Clinical...
