Pharmaceutical Clinical Associates, LLC
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Summit,
NJ
Primary - CRF Design/Coordination Activities
Coordinate shipping requests of CRFs (and other materials as needed) for all domestic and international clinical studies
Monitor inventory at print vendor(s) for availability of supplies for all clinical studies
Assist in the development of CRFs and Guidelines
Maintain printed CRF library
Provide input and help maintain Celgene standard CRF completion guidelines
Routinely interface with cross-functional team members
Participate in project meetings when appropriate, i.e. CRF review meetings
Secondary - Data Management Activities
Assist with clinical data entry as needed
Assist in Data Management tasks as needed
Experience and Skills:
Bachelor’s degree in life science, computer science, or related field, preferred
2 plus years Pharmaceutical or CRO industry experience
Experience using PageMaker
Experience using Word
Experience and knowledge of the drug development process
Excellent interpersonal, communication, and organizational skills
Additional Information:
Job Level: Mid Career (2+ years)
Number of Openings: 1
Years of Experience: At least 2 Years
Level of Education: BA/BS
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.
Summit, NJ
Summit, New Jersey
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