Clinical Trials Management Associate
Listed on 2026-07-01
-
Research/Development
Clinical Research, Research Assistant/Associate, Research Scientist
Clinical Research Associate
Requirements:
• Must meet all requirements for the Clinical Research Associate position and have demonstrated proficiency in all relevant areas.
• Drafts and coordinates review of protocols, informed consents, case report forms, and monitoring plans.
• May participate in abstract presentations, oral presentations, and manuscript development.
• With limited supervision conducts site evaluations/initiations and closeout visits in addition to routine monitoring visits, as required.
• Ability to develop tools and processes that increase measured efficiencies of the project
Top 3 skills:
• Working knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of routine clinical trials.
• Assists in the review of routine data and preparation of safety, interim, and final study reports, and resolution of data discrepancies.
• Assists in CRO or vendor selection. With guidance from the supervisor coordinate CROs or vendors.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).