A company is looking for a Clinical Trial Associate to oversee site management activities for clinical trials.Key ResponsibilitiesOversee day-to-day site management activities to ensure compliance with study protocols and regulatory requirementsCollaborate with site staff and cross-functional teams to resolve issues and ensure timely data collectionAssist with site initiation, monitoring visits, and close-out activities while maintaining site management documentationRequired QualificationsBachelor's degree in life sciences, clinical research, or a related fieldExtensive experience in site management, clinical operations, or monitoring within the clinical research industryStrong understanding of clinical trial processes, Good Clinical Practice (GCP), and regulatory requirementsAbility to manage multiple sites and timelines effectivelyExperience in providing guidance and mentorship to junior staff