CTA - East Coast

As a CTA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will assist the CTM and CTT with the coordination of the logistical aspects of the assigned trial(s), according to Good Clinical Practice (GCP) and the applicable Standard Operation Procedures (SOPs). You will also develop and adapt documents to trial specific requirements in collaboration with the CTM. You will assist with organizing trial specific meetings, including but not limited to trial team meetings and Investigator Meetings. Responsibilities also include coordinating the filing of Trial Master File (TMF) documents in the (electronic) Trial Master File (TMF) part of ECO by reviewing completeness and correct use of ECO.