Fulfillment Center Associate
Qurate Retail Group
Virtual CRC Event
Medpace
full-time
Posted on:
Location: California, Massachusetts, New York, North Carolina • 🇺🇸 United States
Visit company websiteJob Level
Junior
Tech Stack
Google Cloud PlatformSaltStack
About the role
- Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol
- Communication with the medical site staff including coordinators, clinical research physicians, and their site staff
- Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff
- Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements
- On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward
- Verification that the investigator is enrolling only eligible subjects
- Regulatory document review
- Medical device and/or investigational product/drug accountability and inventory
- Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol
- Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement
- and Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance
Requirements
- Must have a minimum of a Bachelor’s degree in a health or science related field
- Experience as a Clinical Research Coordinator (minimum 1.5 years)
- Ability to travel 60-70% to locations nationwide is required; some visits may be conducted remotely
- Must maintain a valid driver’s license and the ability to drive to monitoring sites
- Proficient knowledge of Microsoft® Office
- Strong communication and presentation skills
- Must be detail-oriented and efficient in time management
