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Clinical Trials Administrator

3 months ago

Birmingham, Birmingham, United Kingdom Re:Cognition Health Full time

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
Birmingham.

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:
£24, ,000 per annum, Depending on experience