Clinical Research Associate - Phase II/III Trials

About the Role

Our client is seeking an experienced Clinical Research Associate (CRA) to join their expanding team in Birmingham , contributing to the critical oversight of Phase II and III clinical trials. You will be instrumental in ensuring the safety and integrity of study data by conducting site visits, monitoring trial progress, and verifying compliance with protocols and regulatory requirements. This role is ideal for a meticulous and organized professional passionate about advancing pharmaceutical research and ensuring patient safety throughout the trial lifecycle. Working within a hybrid model, you'll balance on-site activities with remote work, offering flexibility while maintaining crucial site relationships.

Key Responsibilities

• Conduct pre-study, initiation, monitoring, and close-out visits for clinical trial sites to ensure compliance with protocols, GCP , and regulatory standards.
• Monitor data collection and reporting for accuracy, completeness, and adherence to study plans and regulatory guidelines .
• Serve as the primary point of contact for assigned clinical sites, fostering strong relationships with investigators and site staff.
• Identify and resolve site-level issues, escalate concerns promptly, and implement corrective action plans as needed.
• Ensure timely submission of regulatory documents and manage investigational product accountability at trial sites.
• Prepare detailed monitoring reports and maintain accurate trial documentation in line with pharmaceutical industry standards.

Requirements

• Bachelor's degree in a life science, nursing, or related field; advanced degree preferred.
• Minimum of 3 years of experience as a Clinical Research Associate , preferably within a pharmaceutical or CRO setting.
• Thorough understanding of Good Clinical Practice (GCP) , ICH guidelines, and relevant regulatory requirements.
• Proven ability to manage multiple clinical trial sites simultaneously and effectively.
• Excellent communication, interpersonal, and organizational skills, with strong attention to detail.
• Proficiency in clinical data management systems and electronic trial management systems (eTMF).

Benefits

• Competitive annual salary with potential for performance-based incentives.
• Hybrid work arrangement offering a blend of remote and on-site engagement.
• Comprehensive medical, dental, and vision coverage.
• Company car or mileage reimbursement for site visits.
• Opportunities for professional development and career progression within a leading pharmaceutical company .