FULL-TIME
Posted Sep 15, 2026
Job Description
Responsibilities
• Trial Execution: Drive day-to-day protocol compliance, patient recruitment, enrollment, and study visit procedures for active trials.
• Clinical Coordination: Manage study documentation, regulatory binders, source docs, and data entry in coordination with QA/QC specialists.
• Team Collaboration: Work alongside PIs, APPs, and fellow CRCs to ensure trial throughput and high-quality management.
• Therapeutic Focus: Support leading-edge clinical trials focused primarily on Hepatology (liver disease), Chronic Diseases, Weight Loss.
Required Skills
• Minimum 2 years of clinical research experience.
• Familiarity with GCP, regulatory guidelines, and clinical trial documentation/workflows.
• Background or interest in Hepatology/Liver Disease or Chronic Disease protocols.
• Ability to work fully on-site and split time between Westlake and Brooklyn, OH.
• Immediate availability to start ASAP.
• Trial Execution: Drive day-to-day protocol compliance, patient recruitment, enrollment, and study visit procedures for active trials.
• Clinical Coordination: Manage study documentation, regulatory binders, source docs, and data entry in coordination with QA/QC specialists.
• Team Collaboration: Work alongside PIs, APPs, and fellow CRCs to ensure trial throughput and high-quality management.
• Therapeutic Focus: Support leading-edge clinical trials focused primarily on Hepatology (liver disease), Chronic Diseases, Weight Loss.
Required Skills
• Minimum 2 years of clinical research experience.
• Familiarity with GCP, regulatory guidelines, and clinical trial documentation/workflows.
• Background or interest in Hepatology/Liver Disease or Chronic Disease protocols.
• Ability to work fully on-site and split time between Westlake and Brooklyn, OH.
• Immediate availability to start ASAP.
Additional Details
- City
- Westlake
- State
- Ohio
- Country
- US
Apply and matching require a free OVN account. Browse listings anytime without signing in.