Clinical Trial Associate
Tech Observer•Billerica, MA
277d
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About The Position
The position involves coordinating and performing various tasks related to the collection, distribution, and storage of data and study materials generated during clinical research trials. The individual will ensure that assigned trials comply with applicable regulations, Good Clinical Practice (GCP), protocols, and Standard Operating Procedures (SOPs) set by the Tech Observer and Sponsor. Responsibilities include maintaining databases of patient information, assisting with grant proposals, and managing communication with investigators and project teams.
