Jordan Griffiths is currently seeking a highly motivated Clinical Research Associate (CRA) to join their top CRO clients. As a CRA, you will be responsible for the execution and management of clinical trials, ensuring adherence to study protocols, regulatory requirements, and timelines.
Key Responsibilities:
* Conduct site initiation, monitoring, and close-out visits
* Ensure compliance with study protocols, GCP, and applicable regulatory guidelines
* Perform source data verification and review study documents
* Track and report patient enrollment and study progress
* Monitor study drug supply and accountability
Requirements
Requirements:
* Bachelor's degree in a health-related field or equivalent
* 2+ years of Onsite monitoring
* Good understanding of clinical trial processes and regulatory requirements
* Strong attention to detail and organizational skills
* Excellent communication and interpersonal skills
* Ability to work independently and as part of a team
Benefits
* Competitive salary
* competitive benefits
* Car allowance
Whatever your career goals, my client is here to ensure you get there! If you are an experienced CRA looking for a new and exciting opportunity with a lot of room for career progression then please get in touch! To apply, please submit your resume at:
E: Jordan@alsolutions.co.uk