Pharmaceutical Clinical Associates, LLC
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Union,
NJ
Responsibilities will include, but are not limited to, the following:
1. Create an electronic repository to organize and store information from hundreds of clinical sites across numerous clinical studies.
2. Follow Celgene SOPs
3. Verify accuracy of information on clinical site documentation
4. Adherence to required review timelines
5. Liaise with functional source areas (Celgene clinical operations and various clinical research organizations) to ensure documents are compliant
6. Sign off on study drug release documentation
Experience and Skills:
Skills/Knowledge Required:
* Minimum 2 years pharmaceutical R&D experience
* Strong technical skills with Microsoft office (Word, Excel, Powerpoint)
* Ability to think strategically and organize complex tasks
* Strong organizational skills
* Strong communication skills
* Able to navigate Electronic Document Management Systems
* Detail oriented
Additional Information:
Job Level: Any
Number of Openings: 1
Years of Experience:
Level of Education: Any
Salary: TBD
Starting Date : TBD
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Pharmaceutical Clinical Associates is always accepting employment inquiries from professionals interested in our opportunites. If you are interested in career opportunities at Pharmaceutical Clinical Associates please use our online resume formto apply. Pharmaceutical Clinical Associates is an Equal Opportunity Employer.
Union, NJ
Union, New Jersey
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