Clinical Research Coordinator at Velocity Clinical Research, Inc. in High Wycombe

Overview

Apply for Clinical Research Coordinator at Velocity Clinical Research, Inc. in High Wycombe, ENG, GB.

This full‑time on site position offers great opportunities for career growth.

We are seeking a dedicated Clinical Research Coordinator to join our dynamic research team. The successful candidate will be responsible for overseeing and coordinating clinical trials, ensuring compliance with regulatory standards, and maintaining accurate documentation. This role offers an excellent opportunity for individuals passionate about advancing medical science and improving patient outcomes.

Responsibilities

• Coordinate and manage all aspects of clinical trials, including participant recruitment, scheduling, and follow‑up.
• Ensure adherence to study protocols, regulatory requirements, and ethical standards.
• Collect, record, and maintain accurate trial data in accordance with Good Clinical Practice (GCP) guidelines.
• Liaise with investigators, healthcare professionals, and study participants to facilitate smooth trial operations.
• Monitor participant safety and report adverse events in compliance with regulatory procedures.
• Prepare and submit necessary documentation to ethics committees and regulatory authorities.
• Assist in training new staff or interns involved in the research projects.
• Maintain organized records of all trial‑related documentation for audit purposes.

Requirements

• Bachelor’s degree in health sciences, nursing, or a related field.
• Relevant experience in clinical research is preferred.
• Strong organizational skills with the ability to manage multiple tasks efficiently.
• Excellent communication skills to liaise effectively with team members, participants, and external agencies.
• Knowledge of GCP guidelines and regulatory requirements pertinent to clinical trials.
• Ability to work independently as well as part of a multidisciplinary team.
• Proficiency in data management software and Microsoft Office Suite.
• Attention to detail and a high level of accuracy in documentation.
• Prior experience working within healthcare or research environments is advantageous but not essential.

Compensation

Full time. £30,000.00-£40,000.00 per year.

Benefits

• Company pension
• Employee discount
• Enhanced maternity leave
• Free parking
• Health & wellbeing programme
• Referral programme
• Sick pay

Work Location & Authorization

Work Location: In person. Work authorization: United Kingdom (required).