Clinical Research Associate

About the Role

Our client is seeking a meticulous and experienced Clinical Research Associate (CRA) to join their dynamic team based in Coventry . This role is crucial for overseeing clinical trials, ensuring adherence to protocols, and maintaining data integrity. You will work on cutting-edge pharmaceutical projects, contributing to the development of life-changing medications. This position offers a hybrid working model, blending home-based flexibility with essential on-site collaboration and site monitoring activities. The ideal candidate possesses strong organizational skills and a commitment to regulatory compliance within the pharmaceutical sector.

Key Responsibilities

• Monitor clinical trial sites to ensure compliance with protocols, Good Clinical Practice (GCP), and regulatory requirements.
• Verify the accuracy, completeness, and consistency of clinical data by reviewing source documents and case report forms.
• Manage and maintain essential trial documents, ensuring they are up-to-date and readily available for inspection.
• Serve as the primary point of contact for assigned clinical trial sites, addressing queries and resolving issues promptly.
• Facilitate communication between study sites, the clinical operations team, and other relevant stakeholders.
• Participate in the recruitment and selection of new study sites, conducting feasibility assessments as needed.

Requirements

• Bachelor's degree in a life science, nursing, or related field; Master's degree preferred.
• Minimum of 3 years of experience as a Clinical Research Associate or in a similar role within the pharmaceutical industry.
• In-depth knowledge of GCP guidelines and regulatory requirements for clinical trials.
• Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
• Excellent communication, negotiation, and problem-solving skills.
• Ability to travel to clinical trial sites as required for monitoring and oversight.

Benefits

• Competitive annual salary with potential for performance-based bonuses.
• Comprehensive private medical, dental, and vision insurance plans.
• Generous annual leave allowance and public holiday time off.
• Opportunities for professional development and advanced training in clinical research methodologies.
• Hybrid working arrangement providing a balance between home and office-based work.