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 Job #02615 Email this job to a friend
About our client
This is a long-term contract opportunity with a privately held biomedical company focused on the treatment of CNS disorders.
Position Location
Contract Clinical Research Associate Illinois
Salary Reports to
Highly competitive package, commensurate with experience Management
Responsibilities
1) Ensure study documents (e.g., case report forms, source documents and adverse events) are reviewed and tracked to ensure completeness and accuracy
2) Review, clarify and obtain data changes via query with site personnel and lead team members in reviewing data listings and writing queries
3) Draft, compile and verify clinical data for status reports
4) Assist the Clinical Project Manager in preparing the necessary tools to maintain consistency in study data across all sites and regional monitors
5) Track and manage the distribution of study drug and clinical supplies
6) Assist in the development of study timelines and ensure compliance with study timelines
7) Ensure site visits are conducted in compliance with study protocols, FDA regulations and ICH requirements relative to clinical research
8) Assist with the management of vendors and associated data
Requirements
1) RN degree
2) Experience in medical device and CNS preferred
3) Minimum 4 years of field monitoring experience
4) At least 4+ years of experience as a Clinical Research Associate
5) Experience with medical device trials
6) Monitoring experience on in-patient studies
7) Experience as a home-based CRA
8) Excellent communication skills
9) Willingness to travel – up to 50% (weekly basis)

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