Clinical Trial Associate (CTA)
A Global Biopharmaceutical corporation is seeking to hire a Clinical Trials Associate to provide support in the daily activities of managing and coordinating the operational efforts in the development and implementation of research-driven, Investigator Initiated Trials, Cooperative Group and Third Party trials with close collaboration with the Medical Science Liaison/Field managers and research sites.
The Clinical Trials Associate (CTA) will be responsible for: 1) Hands-on management and tracking of all aspects of the IITs/COOPs/3rd Party trials and maintaining study data within the CTMS. 2) Review of study protocols, consent forms, regulatory documents, and submission of IND safety reports, study input and tracking in global company approved clinical trial database, processing clinical drug requests and investigator payments. 3) Study activation activities through completion of publication all while ensuring regulatory integrity and SOP compliance. 4) Maintaining constant knowledge of assigned studies and provide management with study information as requested.
Position: Clinical Trial Associate (CTA)
Location: In-House, New Jersey
Terms: 6 month contract, opportunity for extension.
Pay Rate: $45-52 per hour
Sthree US is acting as an Employment Business in relation to this vacancy.