Clinical Research Associate

About the role

Join our dynamic clinical research team as a Clinical Research Associate. You will be responsible for monitoring clinical trial sites, ensuring compliance with GCP and regulatory requirements.

What you'll do

• •Conduct routine monitoring visits to clinical trial sites
• •Review and verify source documents and case report forms
• •Ensure compliance with study protocols and GCP guidelines
• •Prepare monitoring visit reports and follow-up on findings
• •Support site initiation and closeout activities

What we're looking for

• •2-4 years of CRA experience
• •Strong knowledge of GCP and ICH guidelines
• •Excellent attention to detail
• •Willingness to travel up to 50%

Qualifications

Bachelor's degree in Life Sciences, Nursing, or related field. Master's degree preferred.

Skills