Note: The job is a remote job and is open to candidates in USA. Clinovo is a biotechnology company seeking an experienced Senior Clinical Research Associate (Sr. CRA) to manage and monitor clinical trial sites across Phase I–III studies. The role involves ensuring patient safety, data integrity, and protocol compliance while thriving in a fast-paced environment.

Responsibilities

• Conduct site qualification, initiation, routine monitoring, and closeout visits
• Perform on-site and remote monitoring activities and source data verification (SDV)
• Prepare monitoring visit reports and follow-up letters within required timelines
• Review informed consent forms, protocol deviations, and investigational product accountability
• Maintain study documentation, TMF records, and site compliance
• Build strong relationships with investigators and site personnel
• Identify and escalate site risks, data quality issues, and compliance concerns
• Partner with Clinical Operations, Data Management, Safety, and Regulatory teams
• Support audit and inspection readiness activities

Skills

• Bachelor's degree in Life Sciences, Nursing, or related field
• 5+ years of CRA experience with independent monitoring responsibility
• Required: Experience supporting autoimmune disease clinical trials
• Strong knowledge of ICH-GCP, FDA regulations, and clinical trial conduct
• Experience conducting SIVs, IMVs, COVs, SDV, and site management activities
• Excellent communication, organization, and problem-solving skills
• Ability to travel up to 60%
• Experience working directly for a biopharmaceutical or biotechnology company
• Experience with immunology, cell therapy, or other complex biologic studies
• Experience supporting early-phase clinical trials and academic medical centers

Company Overview

Company H1B Sponsorship