Clinical Research Assistant

Overview

We are seeking a dedicated and detail-oriented Clinical Research Assistant to join our dynamic team. This role offers an exciting opportunity to contribute to cutting-edge clinical studies, ensuring compliance with regulatory standards and supporting the advancement of medical research. The successful candidate will play a vital part in managing data, monitoring patient progress, and assisting in the smooth operation of clinical trials. Prior experience in clinical research or healthcare settings is highly desirable, along with strong organisational and analytical skills. This position is paid and ideal for individuals passionate about contributing to healthcare innovation.

Duties

• Assist in the coordination and management of clinical trials, ensuring adherence to protocols and regulatory guidelines such as FDA regulations.
• Monitor patient progress, recording vital signs, adverse events, and other relevant data with precision.
• Collect, organise, and maintain accurate data using specialised statistical software and data management systems.
• Support patient recruitment, scheduling appointments, and ensuring informed consent procedures are followed correctly.
• Conduct basic analysis of collected data to identify trends or irregularities for review by senior staff.
• Ensure compliance with all ethical standards, including confidentiality and safety protocols.
• Prepare documentation for audits, inspections, and regulatory submissions.
• Assist in training new staff or interns on research procedures and compliance requirements.
• Participate in team meetings to discuss study progress, challenges, and solutions.

Experience

• Previous experience in clinical research or healthcare environments is preferred but not essential; training will be provided for suitable candidates.
• Knowledge of medical terminology and familiarity with clinical research processes are advantageous.
• Experience with statistical software packages (e.g., SPSS, SAS) or data management tools is desirable.
• Understanding of FDA regulations and compliance management within clinical settings is beneficial.
• Proven ability to monitor patients effectively, including basic nursing skills or phlebotomy experience is a plus.
• Demonstrated organisational skills with the ability to manage multiple tasks efficiently while maintaining attention to detail.
• Supervising experience or leadership roles within healthcare or research teams are considered advantageous but are not mandatory.

This role offers a rewarding opportunity to contribute meaningfully to medical advancements while developing valuable skills within a supportive environment.

Pay: £26,190.03-£44,129.89 per year

Work Location: In person