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]