Contract Virtual Clinical Coordinator
About The Position
MCRA, part of IQVIA MedTech, is hiring a Contract Virtual Clinical Coordinator for a fixed-term, six-month assignment. The role supports clinical research studies by conducting remote clinical activities 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 individuals enrolled in or seeking enrollment in clinical studies. The schedule is weekdays from 1:00 PM to 9:00 PM PST, with Saturday and/or Sunday hours from 10:00 AM to 6:00 PM PST. The position works with research teams, study sites, participants, MCRA clinical affairs staff, and clients to support study recruitment, virtual enrollment, participant education and follow-up, data handling, safety monitoring, and study operations. Work is conducted under the guidance of senior MCRA staff as needed.
Requirements
- Bachelor’s degree required; a degree in life sciences or a healthcare-related field is preferred.
- 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.
Nice To Haves
- Bachelor’s degree in a life sciences or healthcare-related field.
Responsibilities
- Follow SOPs and Manuals of Procedures for study activities, maintaining working knowledge of study-specific software applications 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 (GCP).
- Monitor participants for 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
- The posting states that, depending on the position offered, health and welfare benefits may be offered.
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What This Job Offers
Career Level
Mid Level
