Candidate will be responsible for monitoring clinical studies in
compliance with good clinical practice. He/She acts as the primary
liaison between the Clinical Research group and investigational study
sites to ensure the safety of subjects and the accuracy of data. The
RCRA assists the data management groups and the project team in the
processing of all clinical data by ensuring the timely collection of
data and query resolution.
BS Degree Required - 50% travel - Home office potential.
This is a contract position (All contract positions are considered
temporary.)
If you are interested in applying for this position, please send your
resume in a Word format to:
Laurie Meltzer
Tech-Star Recruitment, Inc.
845-480-6462
laurie_...@tech-star.com