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| Company: |
Makro Technologies, Inc. |
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| Job Title: |
Manager Clinical Compliance |
| Employment Category: |
Biotech |
| Job Location: |
NJ New Jersey - USA |
| Job Reference Number: |
MCC_8707 |
| Job Description: |
Urgent requirement for one of our top clients located in “Piscataway, NJ”.
Job Description:
The Manager, Clinical Compliance manages all aspects of Quality Compliance and reports to the Vice President, Global Project Management. The applicant will have primary responsibility for implementing a quality compliance system for Clinical Development, Drug Safety Surveillance and Medical Affairs. The applicant also manages clinical research activities and is responsible for regulatory compliance of all clinical studies, including developing internal and external audit plans. The Manager, Clinical Compliance is responsible for labeling control of clinical supplies and releasing clinical supplies to study sites. Applicant will work closely with Regulatory Affairs, GBM, Clinical and other R&D groups to assure compliance.
Please mention your best hourly rate, availability and visa status. Any questions, do feel free to email us.
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Skills Required:: |
· BA/BS preferably in life science
· Minimum of 5-7 years relevant industry experience in the clinical research area, such as Clinical Trial Monitor/Auditor or Clinical Compliance specialist. |
Language Requirements: |
English-A little
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| Employment Type: |
Full Time
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| Yearly Salary: |
Unspecified
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| Posting Date: |
Aug 07 2007 |
| Education level required: |
Bachelor
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| Experience in years: |
5 to 7 Years |
| Job also available in: |
Piscataway |
| Company: |
Makro Technologies, Inc. |
| Contact Name: |
Anitha |
| Preferred Method of Contact: |
E-mail via Apply Online Box |
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