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Sterling Life Sciences, Specialists in Pharmaceuticals, Healthcare and BioTech Recruitment
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 Job #02745 Email this job to a friend
About our client
Our client is a leading pharmaceutical company, which is focused in the development and commercialization of various therapeutics in disease prevention, aimed to improve the quality of life for everyone worldwide. The company has an experienced management team, a varied selection of protocols and an empowering corporate culture that is focused on the long-term development of its employees.
Position Location
Associate Director – Clinical Data Manager New Jersey
Salary
Highly competitive package, commensurate with experience
Responsibilities
1) Monitor Phase I studies (as necessary)
2) Review regulatory documents
3) Assist with the management of Phase III global studies as well as interface with CROs
4) Review and comment on scope of work and proposals from all vendors
5) Track documents and work flow
6) Review and comment on protocols, CRFs and other study-related documents to ensure quality and consistency
7) Participate in team, study and vendor meetings (as required)
Requirements
1) BS in Nursing
2) Minimum 3 years of experience in the pharmaceutical industry
3) Experience in monitoring, data reviewing and patient profile reviewing
4) Background in sepsis and respiratory preferred
5) Ability to work in a team environment
6) Excellent communication skills
7) Willingness to travel (25% to 30%)

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