Clinical Trial Administrator (CTA)
An opportunity has arisen for a clinical trial professional to join leading European specialist pharmaceutical company as Clinical Trial Administrator in their office in West London.
The role is permanent, full-time and office based for 3 days per week.
You will be responsible for
Providing administrative support for clinical trial activities acting as a central contact for the clinical study team for designated project communications, arranging clinical meetings, compiling agenda and taking Minutes.
Maintaining the Trial Master File (TMF) and electronic TMF (eTMF), performing QC and periodic checks on the completeness
Acting as Deputy/ Nominated Archivist for the company, archiving documents in accordance with GxP guidelines and SOPs
Keeping track of payments to Investigators and ensure they are added to the internal data collection system.
Maintain overall clinical studies oversight via the CDT clinical trial tracker
You will bring
Life Science degree, nursing qualification or equivalent
1+ years of experience in CTA or similar role
Working experience with eTMF/TMF, eCRF, IxRS and CTMS systems
Good understanding of ICH GCP and regulatory requirements for clinical trials
Excellent organization skills, with ability to prioritize and multi-task across several projects.
Ability to work effectively under pressure
'Can-do' attitude, pro-active approach and enthusiastic outlook.
If you don’t want to miss out on this opportunity, please get in touch ASAP.
Phone: 0203 892 8777