Remote Clinical Research Associate
- newcastle upon tyne, tyne and wear, NE1 0DT, United Kingdom
- Permanent·Remote
- Full time
- £55,000 - £55,000 Per Annum
Job Description
About the Role
Our client is seeking a dedicated and meticulous Clinical Research Associate (CRA) to join their fully remote clinical operations team, supporting studies conducted across the UK. This vital role focuses on ensuring the quality, integrity, and compliance of clinical trials by monitoring study sites and verifying data accuracy. You will be empowered to manage your territory effectively from home, contributing significantly to the successful execution of groundbreaking research. This is an ideal opportunity for a self-motivated CRA who thrives in a flexible, home-based work environment and is passionate about advancing medical treatments.
Key Responsibilities
- Conduct site initiation, interim monitoring, and close-out visits for clinical trials, adhering strictly to protocols and regulatory guidelines.
- Verify the accuracy, completeness, and consistency of clinical data by reviewing source documents and electronic data capture systems.
- Ensure compliance with protocol requirements, Good Clinical Practice (GCP) , and all applicable regulations.
- Communicate effectively with investigators, site staff, and internal project teams to address any study-related issues or queries promptly.
- Manage study documentation and ensure all essential documents are maintained and filed appropriately in the Trial Master File (TMF).
- Identify potential risks and develop mitigation strategies to ensure trial timelines and quality objectives are met.
Requirements
- Bachelor's degree in Life Sciences, Nursing, or a related field.
- Proven experience as a Clinical Research Associate , with a strong understanding of GCP and regulatory requirements.
- Demonstrated ability to conduct comprehensive site monitoring visits and manage multiple clinical trials simultaneously.
- Excellent organizational, analytical, and problem-solving skills.
- Strong written and verbal communication skills, with the ability to build rapport with site personnel.
- Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) tools.
Benefits
- Competitive annual salary commensurate with experience.
- Fully remote work arrangement offering excellent work-life balance.
- Comprehensive private medical insurance and life assurance.
- Company car allowance or mileage reimbursement for travel to sites.
- Generous annual leave and public holiday entitlement.


