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Sterling Life Sciences, Specialists in Pharmaceuticals, Healthcare and BioTech Recruitment
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 Job #02388 Email this job to a friend
About our client
Our client is a reputable, mid-size CRO that is experiencing unprecedented growth. The company has an experienced management team, a varied selection of interesting protocols and an empowering corporate culture that is focused on the long-term professional development of its employees.
Position Location
Clinical Research Associate New Jersey
Salary
Highly competitive package, commensurate with experience
Responsibilities
1) Monitor clinical trial from site evaluation to close out
2) Collect data and quality control review of data collected at sites
3) Ensure compliance with multiple protocols, FDA regulations and GCP guidelines for Phase II, III and IV trials
Requirements
1) Bachelor’s degree in a scientific discipline
2) 2+ years of clinical trial experience in the pharmaceutical or biotech industry
3) 2+ years of field monitoring experience
4) Experience in monitoring clinical trials from qualification to closeout
5) Experience in Cardiology/Oncology/Rheumatology
6) Strong knowledge and understanding of FDA Regulations and GCPs
7) Exceptional communication skills
8) Willingness to travel

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