Senior Clinical Research Associate

About the Role

Our client is seeking an experienced and dedicated Senior Clinical Research Associate (CRA) to join their dynamic, fully remote team. This pivotal role involves overseeing clinical trials, ensuring compliance with protocols, and maintaining high standards of data integrity. You will be instrumental in the successful execution of studies, contributing directly to the advancement of new pharmaceutical products. This is a fantastic opportunity for a seasoned professional who thrives in a remote setting and possesses a deep understanding of regulatory requirements and clinical trial processes, joining a company that fosters a culture of innovation and excellence.

Key Responsibilities

• Conduct site initiation, monitoring, and close-out visits to ensure adherence to study protocols and regulatory guidelines.
• Verify the accuracy, completeness, and consistency of clinical trial data through source document verification.
• Manage communication between study sites, investigators, and the core project team, resolving issues promptly.
• Ensure all study-related documentation is maintained and updated accurately in the trial master file.
• Provide guidance and support to clinical site staff, fostering strong working relationships.
• Prepare and submit regular progress reports on study status and site performance.

Requirements

• Bachelor's degree in a life science, nursing, or related field; advanced degree preferred.
• Minimum of 5 years of experience as a Clinical Research Associate in the pharmaceutical industry.
• Thorough knowledge of Good Clinical Practice (GCP) , ICH guidelines, and applicable regulatory requirements.
• Proven experience in monitoring clinical trials across various therapeutic areas.
• Excellent organizational, communication, and interpersonal skills, with a strong attention to detail.
• Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.

Benefits

• Competitive annual salary.
• Fully remote working environment with flexible hours.
• Comprehensive private medical insurance.
• Generous annual leave allowance.
• Opportunities for professional development and career advancement.
• Contribution to a leading-edge pharmaceutical research environment.