Clinical Trial Associate: Work for a small CRO
Clinical Trial Associate: Learn, Grow and Succeed!!
My client is looking for a CTA for work (flexible conditions) in the Ghent region. The company is a well know pharmaceutical company in Belgium and they are eager to bring in a motivated professional who already has a 1 or 2 years experience. The position has opened up because of new business, and there will be more and more opportunities thanks to the company performance. Below are the main tasks of the role, if you have further questions please don't hesitate to get in touch with me.
Assists the CTM 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):
Assists with signature collection for CDAs, contracts, POs and insurance certificates in collaboration with CTM/Director Vendor Management
Develops and adapts documents to trial specific requirements in collaboration with the CTM
May assist with the preparation of trial reports for the trial team and keeping them up-to-date
Assists with organizing (agenda, meeting minutes, follow-up on action items) trial specific meetings, including but not limited to trial team meetings, Investigator Meetings.
Assists the CTM/COL to ensure that the essential Trial Documents at sponsor level are properly filed and made ready for archiving. Provides input to the other departments outside Clinical Operations to ensure that the needed documents are filed within the (e)TMF.
Assists in (electronic) Trial Master File review (TMF) to confirm completeness and follow-up of findings
The CTA may assist COL with:
The organisation of the clinical team meetings (agenda, meeting minutes, follow-up on action items)
The CTA helps the Head of Clinical Operations with:
The development of template documents to be used within the Department
The organization of the departmental meetings (agenda, meeting minutes, follow-up on action items)