Clinical Research Associate

About the Role

Our client is seeking a meticulous and dedicated Clinical Research Associate to join their dynamic clinical operations team in Newcastle upon Tyne . This role is crucial for ensuring the integrity and quality of clinical trials by monitoring study sites and ensuring compliance with protocols, regulations, and Good Clinical Practice (GCP). You will act as a key liaison between the study sponsors and investigative sites, facilitating smooth trial execution. This hybrid position offers the flexibility to work from home and visit sites in and around the Newcastle area, contributing to life-changing medical advancements.

Key Responsibilities

• Conduct site initiation, monitoring, and close-out visits according to study protocol and SOPs.
• Ensure accurate data collection, source document verification, and adherence to regulatory requirements.
• Build and maintain strong relationships with investigators, site staff, and study participants.
• Identify, resolve, and document study-related issues and risks effectively.
• Prepare detailed monitoring visit reports and ensure timely follow-up actions are completed.

Requirements

• Bachelor's degree in a life science, nursing, or related field.
• Minimum of 2 years of experience as a Clinical Research Associate or in a similar monitoring role.
• Thorough understanding of ICH-GCP guidelines and relevant regulatory requirements.
• Excellent organizational, communication, and interpersonal skills.
• Ability to travel to clinical sites as required for monitoring activities.

Benefits

• Competitive salary package commensurate with experience.
• Mileage and expense reimbursement for travel.
• Comprehensive benefits including health, dental, and paid time off.
• Opportunities for career advancement within clinical research.
• A supportive and collaborative team environment in Newcastle upon Tyne .