Contract Virtual Clinical Coordinator
About The Position
The Contract Virtual Clinical Coordinator is a fixed-term, 6-month position supporting clinical research studies through remote clinical activities conducted in accordance with study protocols, Standard Operating Procedures (SOPs), and Good Clinical Practice (GCP). The coordinator performs clinical procedures to collect, record, report, and interpret patient data for people enrolled in or seeking enrollment in clinical studies. The schedule includes weekday hours from 1:00 PM to 9:00 PM PST and Saturday and/or Sunday hours from 10:00 AM to 6:00 PM PST. MCRA is part of IQVIA MedTech, which provides integrated lifecycle solutions for the medical device and diagnostics industry. The role works with research teams, study sites, participants, MCRA clinical affairs staff, and clients to support clinical research operations.
Requirements
- Bachelor’s degree required, preferably in a life sciences or healthcare-related field.
- At least three years of experience as a Clinical Coordinator or in a comparable clinical research role.
- Strong attention to detail.
- Excellent verbal and written communication skills.
Responsibilities
- Follow SOPs and Manuals of Procedures for study activities, maintaining working knowledge of study-specific software and equipment.
- Collaborate with research teams and study sites to identify, recruit, and virtually enroll eligible clinical trial participants.
- Collect, maintain, and securely store clinical research data in accordance with regulatory and organizational standards.
- Educate potential participants about clinical trials and study requirements, and manage the informed consent process through virtual interactions.
- Support participant compliance by providing guidance and reminders about protocol requirements.
- Conduct clinical trial follow-up activities in accordance with Good Clinical Practice guidelines.
- Monitor participant safety, promptly report adverse events, and ensure compliance with IRB-approved protocols.
- Support the research participant call center as assigned by handling inquiries and providing assistance.
- Maintain professionalism in interactions with research participants to foster trust and engagement.
- Assist with study equipment management and reporting, including tracking, functionality, and documentation.
- Communicate with MCRA clinical affairs staff and clients, providing updates and support under the guidance of senior MCRA staff as needed.
- Perform additional duties and projects as assigned to support clinical research operations.
Benefits
- A range of health and welfare benefits may be offered, depending on the position.
