Clinical Research Associate - UK

We are currently looking for a “Clinical Research Associate” to join a leading pharmaceutical company based in the UK area. As the Clinical Research Associate, you will be responsible for ensuring the integrity of clinical trials and contributing to the advancement of medical research.

KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Clinical Research Associate will be varied however the key duties and responsibilities are as follows:
1. Overseeing the progress of clinical trials and ensuring compliance with regulatory requirements.
2. Conducting site visits to monitor study protocols and ensuring data accuracy.
3. Collaborating with investigators and site staff to resolve any issues and ensure smooth trial operations.
4. Preparing detailed reports and documentation to support clinical trial activities.

ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Clinical Research Associate, we are looking to identify the following on your profile and past history:
1. Relevant degree in a life sciences field.
2. Proven industry experience in clinical research.
3. A working knowledge and practical experience with Good Clinical Practice (GCP) guidelines.

Key Words: Clinical Research Associate / Clinical Trials / Pharmaceutical / GCP / Site Monitoring / Regulatory Compliance / Data Accuracy / Investigator Collaboration / Clinical Study / Medical Research

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.