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.

Email: Valerie.kalna@biotalent.com
Phone: 0203 892 8777