Pharmaceutical Clinical Research Associate (CRA)

About the Role

Our client is seeking a dedicated and meticulous Pharmaceutical Clinical Research Associate (CRA) to support their clinical trial activities in and around the Plymouth area. In this critical role, you will be responsible for monitoring clinical trial sites to ensure compliance with protocols, regulations, and ethical standards. You will play a key part in collecting high-quality data, safeguarding patient well-being, and ensuring the integrity of clinical research studies that advance new pharmaceutical treatments. This field-based position offers the opportunity to travel and interact directly with investigative sites.

Key Responsibilities

• Conduct site initiation, monitoring, and close-out visits according to clinical trial protocols and Standard Operating Procedures (SOPs).
• Verify the accuracy, completeness, and consistency of clinical data recorded in Case Report Forms (CRFs) and electronic data capture systems.
• Ensure compliance with protocol, Good Clinical Practice (GCP), and all applicable regulatory requirements at investigational sites.
• Build and maintain positive relationships with investigators, site staff, and study participants.
• Identify and report any deviations, adverse events, or safety concerns promptly.
• Manage investigational product accountability and ensure proper storage and handling.

Requirements

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
• Minimum of 2 years of experience as a Clinical Research Associate or in a similar clinical trial role.
• Thorough understanding of GCP guidelines and regulatory requirements for clinical trials.
• Excellent organizational, communication, and interpersonal skills.
• Ability to travel regularly to assigned clinical trial sites.

Benefits

• Competitive annual salary and performance-based incentives.
• Company car and travel expenses reimbursement.
• Comprehensive health, dental, and vision insurance.
• Generous paid time off and holiday schedule.
• Opportunities for professional growth and advancement within clinical research operations.