Clinical Trials Administrator - Guildford, United Kingdom - Re:Cognition Health

Re:Cognition Health

Verified Company

Guildford, United Kingdom

1 week ago

Posted by:

Tom O´Connor

beBee Recruiter

Description

About the Company:

Re:
Cognition Health is a leading provider of clinical services specializing in cognitive impairment.

We deliver expert clinical care to private patients and are one of the foremost providers of clinical trials in the world and deliver award winning medico-legal services.

We value people who are dedicated, hardworking and looking to contribute to the growth of the business at an exciting time.

The Clinical Trials Administrator Role:

We have an opportunity within the organization for confident Clinical Trial Administrator to join a talented growing team. The position is based in
Guildford.

We are looking for an ambitious, organized and hardworking individual, willing to take on a range of responsibilities and grow with the company.

You will be providing support and assistance in the administrative management of the clinical trial studies. Working closely with the Study Coordinator, Principal Investigator and Senior Management teams to maintain and organise study files.

The CTA will be involved in most activities in preparation for study set up, conduct and completing a Clinical Trial.

Responsibilities:

Providing administrative support to the Clinical Trial Coordinator and PI
Preparing CRFs (Source documents) and other essential documents
Assist with collating, submitting and tracking source data and data queries to Data Management within the set timeframes
Maintenance of Investigator Site File (ISF)
Maintenance of study documents and trial supplies
Assist with laboratory sample management, including processing laboratory samples
Assist with pharmacy checks
Maintaining clinical trial databases

Requirements:

BSc educated in life sciences
Previous administration experience in a clinical setting
IT Proficiency (Microsoft Office package)
Good verbal and written communication skills

Desirable:

Clinical trials experience in an NHS, academic or commercial setting
Experience of managing essential documents for clinical trials according to ICH GCP
Experience of using electronic data capture systems, e.g. medidata RAVE

Benefits: