Clinical Trials Administrator - Re:Cognition Health

Re:Cognition Health (London based) is a pioneering brain and mind clinic that specializes in the treatment and care of people showing symptoms of cognitive impairment. Utilizing the latest progressive medical research and evidence-based treatments, we are passionate about transforming and optimizing cognitive performance through education, clinical excellence and by providing access to emerging treatments. This is an exciting time in the history of Re:Cognition Health in light of, through its US subsidiary, its current expansion in the US.

We value people who are dedicated, hardworking and looking to contribute to the growth of our business. Our vision is to become the recognized worldwide leader in the diagnosis, treatment and care management of individuals experiencing cognitive impairment. Come join our team where everyone is valued and where critical and important work is being done!

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 successful applicant will have access to all Re:Cognition Health’s benefits. On top of this the successful candidate will have the opportunity to work in one of our established clinics around the country.

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 Winchester. 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

• Continuous professional development
• Private Health Insurance
• Pension Scheme
• Employee Assistance Program
• Life Insurance

Type of Contract:

Permanent

Working schedule:

40 hours per week, Full time

Salary:

£26,500 - 28,000 per annum, Depending on experience