Job Details

A company is looking for a Clinical Trial Specialist to oversee site management activities for clinical trials.Key ResponsibilitiesOversee day-to-day site management activities ensuring 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 providing guidance to junior staffRequired 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 preparing and maintaining site management documentation