Clinical Trial Coordinator

CK Group- Science, Clinical and Technical; Torpoint; On-site; GBP 60,000 - 80,000; Full time

Job summary

A leading provider in the life sciences industry is looking for a Clinical Trial Coordinator in Torpoint, Cornwall. The role involves providing clinical research support, data management, and maintaining study files. Candidates should have a relevant scientific degree and knowledge of clinical trials. This contract position offers £20 to £25 per hour based on experience.

Qualifications

• Hold a relevant scientific degree or equivalent working experience.
• In-depth knowledge of departmental, protocol and study-specific operating procedures.
• Knowledge of medical terminology.

Responsibilities

• Provide clinical research support to investigators and site staff.
• Input research study data into trial Electronic Data Capture (EDC) system.
• Collect and submit regulatory/ethics documentation.

Skills

Knowledge of clinical trials

Excellent eye for detail and accuracy

Education

Relevant scientific degree or equivalent working experience

Job description

CK Group are recruiting for a Clinical Trial Coordinator (CTC) to join a leading provider of advanced analytics, research and technology solutions to the life sciences industry on a contract basis for 12 months.

Salary: £20 to £25 per hour PAYE, depending upon experience.

Clinical Trial Coordinator Role

• Provide clinical research support to investigators and site staff.
• Verify and/or correct research study information on source documents, research queries and variances.
• Input research study data into trial Electronic Data Capture (EDC) system, maintaining quality control for content.
• Prepare and maintain research study files.
• Maintain the FDA 1572 form for assigned research studies.
• Collect and submit regulatory/ethics documentation pertaining to the research study.
• Input visit data into the clinical trial management system (CTMS) to track patient visits.

Your Background

• Hold a relevant scientific degree or equivalent working experience.
• Knowledge of clinical trials.
• In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules.
• Knowledge of medical terminology.
• Excellent eye for detail and accuracy.

Company

Our client offers research services and technology solutions in the life sciences industry. With just under 100,000 employees, the company has operations in over 90 countries worldwide. Our client’s ambitions involve optimising results of innovations using artificial intelligence. They believe in utilising data collected to the maximum rather than focussing on gathering lots of information: they use artificial intelligence to do this.

Location

This role is based at our client’s site in Torpoint, Cornwall.

Apply

For more information, or to apply for this Clinical Trial Coordinator please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (Apply online only).

It is essential that applicants hold entitlement to work in the UK.

Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.