Clinical Research Associate

About the Role

Our client is actively searching for a meticulous and motivated Clinical Research Associate (CRA) to join their expanding team, focusing on clinical trials within the Coventry region. In this vital role, you will be responsible for ensuring the smooth and compliant execution of clinical studies, overseeing site operations, and safeguarding the integrity of data collected. You will collaborate closely with investigators, site staff, and internal project teams to facilitate the successful progression of research, ultimately contributing to the development of new therapies. This position offers a fantastic opportunity to play a key part in cutting-edge pharmaceutical research, working in a collaborative environment that values scientific rigor and patient safety within the West Midlands .

Key Responsibilities

• Conduct site selection, initiation, monitoring, and close-out visits to ensure compliance with protocols and regulatory requirements.
• Verify the accuracy, completeness, and validity of clinical trial data through source data verification and review of case report forms.
• Manage relationships with investigators and site staff, providing guidance and support to facilitate study progress.
• Ensure adherence to Good Clinical Practice (GCP) guidelines, company SOPs, and all applicable regulations.
• Prepare and present site monitoring reports, identifying potential issues and proposing solutions.
• Facilitate regulatory audits and client inspections at assigned clinical trial sites.

Requirements

• Proven experience as a Clinical Research Associate or in a similar clinical trial monitoring role.
• Solid understanding of clinical trial processes, ICH-GCP guidelines, and relevant regulatory frameworks.
• Excellent monitoring skills, including meticulous attention to detail and proficiency in data verification.
• Strong organizational, communication, and problem-solving abilities.
• Bachelor's degree in a life science, nursing, or related discipline; advanced degree preferred.
• Ability to travel frequently to clinical sites within the assigned territory, including occasional overnight stays.

Benefits

• Competitive salary commensurate with experience.
• Generous travel allowance and expense reimbursement.
• Comprehensive benefits package including health, dental, and life insurance.
• Opportunities for professional growth and advancement within a leading pharmaceutical organization.
• Flexible working arrangements supporting a hybrid work model.