Job Details

A company is looking for a Clinical Research Associate.Key ResponsibilitiesSupport site initiation, ongoing management, and close-out activities in accordance with study timelinesEnsure compliance with study protocol, ICH-GCP, FDA regulations, and company SOPsProvide oversight of CRO CRAsand site management activities, and maintain a compliant Trial Master FileRequired QualificationsBachelor's degree in life sciences, nursing, or a related field; advanced degree preferredMinimum of 3+ years of clinical operations experience in biotech, pharma, or CRO environmentsPrior experience in site management and CRO oversight strongly preferredStrong knowledge of ICH-GCP, FDA regulations, and global clinical trial requirementsExperience with EDC systems, CTMS, eTMF, and safety reporting processes