
Detail-oriented healthcare professional with experience in clinician recruitment, credentialing, and compliance within fast-paced healthcare environments. Strong background in documentation accuracy, data tracking, and maintaining audit-ready records using ATS and VMS systems. Experienced in verifying licensure, coordinating onboarding, and ensuring adherence to regulatory and organizational standards. Knowledgeable in clinical research fundamentals, including Good Clinical Practice (GCP), informed consent, and protocol adherence, with a strong interest in clinical trial operations. Proven ability to collaborate with cross-functional teams, manage competing priorities, and maintain data integrity. Seeking to transition into a Clinical Trials Associate role to support study coordination, regulatory compliance, and research operations.