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Clinical Trials Associate, 6 month contract

Clinical Trials Associate, Buckinghamshire, 6 month contract

Job Summary: Working within a global pharmaceutical giant that has a passion for developing new and innovative products and services to the healthcare market. This role focuses on the delivery of an investigator initiated clinical trial program, so you will be responsible for ensuring regulatory compliance and patient safety, liaison with multiple stakeholders with regards to the extension of study requirements, and to ensure successful inspections and audits through administrative excellence and support. Naturally, working within one of the world's top 10 pharmaceutical organisations, you will receive outstanding benefits, and exciting and varied challenges.

Duties & Responsibilities:
Prepare and maintain up-to-date, accurate clinical trial master files to audit/inspection level.
Throughout the clinical trial process, coordinate essential clinical trial documents and tracking.
Assist with study status reporting and completion of trial related tracking documents, as directed.
Collate and distribute clinical trial documents to relevant stakeholders.
Administrate study finance requirements.
Support study drug supplies management processes.
Complete quarterly clinical trial/activity file quality control reviews with (LTM).
Attend, contribute and present at team meetings/teleconferences as required on trial specific items

Person Specification:
It is essential that you have previous CTA experience, ideally across a variety of therapeutics.

If this role is of interest please contact Sarah Goddard on 01189 594990 or sarah@clinicalprofessionals.co.uk

Key Words: Clinical Trial Associate Administrator CTA Buckinghamshire Berkshire pharmaceutical

We are dedicated to the clinical research industry, offering candidates a unique service including our free \"Pipeline Watch\" career advisory consultation. To find out more call us on 0118 9594990 or email apply@clinicalprofessionals.co.uk