Remote Clinical Research Coordinator
Location:
Remote – U.S. Time Zones Preferred
Client:
This position is in partnership with a client of UniTriTeam, a leader in clinical research support and global staffing.
About the Role:
UniTriTeam is seeking a Remote Clinical Research Coordinator (CRC) to support one of our clinical research site clients. This position is fully remote and does not involve in-person patient interaction, but will require coordination and facilitation of remote patient visits, as well as all behind-the-scenes clinical trial support. The ideal candidate has strong communication skills, is detail-oriented, and has experience using CTMS platforms such as CRIO or Clinical Conductor.
Key Responsibilities:
- Coordinate day-to-day clinical trial operations in a remote capacity, ensuring compliance with study protocols and regulatory guidelines.
- Support and facilitate remote patient visits, including scheduling, documentation, and follow-up.
- Patient Recruitment support to include inclusion/exclusion understanding and qualifying patients for studies via phone.
- Maintain accurate and timely data entry in EDC and CTMS systems; manage query resolution.
- Assist with regulatory document management and remote IRB submissions and updates.
- Prepare for and participate in remote sponsor/CRO monitoring visits, audits, and inspections.
- Serve as a virtual liaison with sponsors, CROs, and internal site teams.
- Support study startup and closeout tasks, including remote collection and verification of essential documents.
- Monitor visit schedules and ensure all subject documentation is complete and up to date.
Required Qualifications:
- 2+ years of experience in clinical research coordination or clinical operations.
- Strong understanding of GCP, ICH, and FDA regulatory requirements.
- Proficiency with CTMS platforms – CRIO or Clinical Conductor strongly preferred.
- Fluent in English – both verbal and written communication required.
- Comfortable working independently in a fully remote setting across multiple time zones.
- Highly organized with strong attention to detail and documentation accuracy.
- Proficient in Microsoft Office Suite and remote communication platforms (Zoom, Teams, etc.).
Preferred Qualifications:
- Associate or Bachelor’s degree in health sciences or related field.
- Clinical research certification (e.g., ACRP, SoCRA).
- Prior experience supporting multi-site trials remotely.
- Bilingual proficiency is a plus.
Work Schedule:
Full-time (Remote), U.S. time zones (EST to PST)
Perks of Working with UniTriTeam:
- Work with a mission-driven organization transforming the clinical research industry.
- Fully remote work environment with global team collaboration.
- Exposure to innovative research sites and a wide variety of protocols.
- Professional development and growth opportunities.
- Supportive and inclusive team culture.
