Clinical Research Associate (CRA)

Responsibilities: of the Clinical Research Associate include: · Perform remote monitoring and source data verification activities to ensure study data accuracy, completeness, and regulatory compliance. · Review clinical trial documentation and maintain oversight of study conduct in accordance with protocol requirements and industry regulations. · Collaborate with investigators, site staff, and internal study teams to address data discrepancies and support timely query resolution. · Conduct site initiation visits (SIVs) and participate in onsite monitoring visits when required to support study milestones and quality objectives. · Prepare monitoring reports and maintain essential study records while ensuring adherence to GCP, SOPs, and applicable regulatory standards. Qualifications: for the Clinical Research Associate include: · Minimum of 2 years of source data verification (SDV) experience within clinical research. · Prior monitoring experience supporting in vitro diagnostic (IVD) clinical trials. · Native-level English communication skills with strong written and verbal proficiency. · Ability to support studies and collaborate across all four U.S. time zones. · Willingness to travel within the continental United States for intermittent onsite monitoring visits and site initiation visits. · CLIA Waiver training or experience is preferred. Compensation: for the Clinical Research Associate: Salary Range: $110,000-$130,000/year (USD) Comprehensive Benefits: Medical, Dental, Vision, sick leave if required by law, and 401K This job opens for applications on 10/30/26. Applications for this job will be accepted for at least 30 days from the posting date.