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:
[email protected]