Job Title : TMF Associate Employment Type :Full time, Permanent Job Reports To : Manager, TMF Operations Department/Unit Name : TMF Operations Job Summary : Responsible for the management of the Trial Master File (TMF) content and associated processes during the
Primarily a training and development role, this position will support and observe clinical site monitoring services both inhouse and in the field whilst developing CRA skills and knowledge. This role will have exposure and training in
The Regulatory Affairs Associate will support the preparation, tracking, and coordination of Ethics Committee (EC) and Regulatory Authority (RA) submissions. Under supervision, the Associate will assist the Regulatory Affairs team in ensuring that clinical trial submissions comply with