Clinical regulatory affairs Associate - B

 
Location: Abbott Park, Illinois
Posted On: 3/20/2017
Job Code: 4850
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Category:Non-IT code:new
 
Job Description
 
- This position interacts with multiple departments, as appropriate, involved in regulatory submissions.
- Make FDA submissions, reviews requisite/critical documents and reports for completeness and suitability for submission.
- Specific Responsibilities Receive documents from various sources and review for completeness and suitability for submission to FDA.
- Review regulatory documents to assure FDA requirements are met and are ready for submission.
- Timely review of critical documents for drug release is expected.
- This position might require the management of temporary labor and supervise the assembly of submission, and verify that the documents meet the regulatory requirements
Category:Non-IT  code:new
 
 
Job Requirements
 
 
- At least three to five years of work experience.
- Understanding of scientific disciplines required.
- Experience with regulatory affairs and documentation work.
 

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Recruiter
Sitara Verma
 
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