KEY TASKS & RESPONSIBILITIES
General:
Build strong communication network with all GRA colleagues to provide compliance oversight for key... May-18-2012
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- M.S. and 3+ years of Regulatory experience
- B.S. and 6+ years of Regulatory work experience
- Experience preparing, submitting, and successfully opening an IND with the FDA
- Experie... May-11-2012
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- Must have a minimum of a Masters Degree in the Life Sciences field.
- Must have a minimum of 5-7 years of experience within regulatory affairs, reviewing promotional materials and interacting... May-11-2012
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- M.S. and 2+ years or B.S. and 4+ years of experience in drug development in biotech or pharmaceutical industry required .
Preferred Requirements:
- Self motivated, with the abi... May-11-2012
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•University degree or equivalent in science, medicine, bioengineering or similar
•In depth knowledge of and experience in regulatory processes.
•Good project management skills.
•Ability to cooperat... May-08-2012
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Your Profile
• Master’s Degree or Dipl.-Ing. in Biomedical Engineering or a comparable technical discipline
• 8-12 years of experience in managing international regulatory affai... May-08-2012
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Master's Degree in related field from an accredited college or university and eight (8) years relevant work experience; or equivalent combination of education and experience. Knowle... May-04-2012
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Minimum 7 years experience in pharma or biopharmaceutical enviornment.
Have worked in a GCP environment
Detailed experience in the preparation of content and format of submissions. &nb... May-02-2012
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