Unblinded Clinical Research Coordinator
Listed on 2026-01-27
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Healthcare
Clinical Research
Job Title:
Unblinded Clinical Research Coordinator
Pay Range:Up to $27 per hour
Schedule:Monday - Friday, 8:00 AM - 5:00 PM
Duration:90-day contract with potential for extension or conversion to a permanent position based on performance and trial needs.
Position Summary:This full-time role supports the day-to-day operations of clinical trials, with a strong focus on Investigational Product (IP) management while maintaining study integrity between blinded and unblinded staff. The Unblinded CRC serves as the subject-matter expert for IP handling and works closely with the Site Manager, study team, sponsors, and participants to ensure compliance with protocols and SOPs.
Key Responsibilities:- Managing all aspects of Investigational Product (receipt, storage, dispensing, administration, accountability, and return/destruction)
- Maintaining the study blind and communicating appropriately with blinded and unblinded team members
- Conducting patient-facing visits, including vitals, ECGs, lab collection, and protocol-required procedures
- Completing accurate source documentation and EDC entry within required timelines
- Monitoring study activities for regulatory and protocol compliance
- Recording and reporting adverse events and resolving sponsor queries
- Participating in site audits, monitor visits, investigator meetings, and site initiation visits
- Maintaining temperature logs, pharmacy binders, and master study logs
This position reports directly to the Site Manager/Director and plays a critical role in ensuring studies run smoothly and compliantly.
Required Qualifications:- Recent, heavy hands-on injection or vaccine administration experience, including independent injection administration in accordance with medication protocols
- Patient-facing clinical experience (Medical Assistant, Clinical Research Assistant, Research Assistant, LPN, etc.)
- Ability to work directly with study participants in a clinical setting
- Strong attention to detail and accurate documentation skills
- Ability to complete source documentation during patient visits and enter data into EDC within required timelines
- Ability to follow study protocols, SOPs, and regulatory requirements
- Basic understanding of GCP and FDA regulations (training acceptable)
- Strong communication and organizational skills
- Ability to work Monday–Friday, 8:00 AM–5:00 PM
- Ability to start ASAP
- Previous experience as a Clinical Research Coordinator (CRC)
- Unblinded CRC or Investigational Product (IP) management experience
- Experience with drug accountability, temperature logs, and pharmacy binders
- Experience with Investigational Product preparation and administration
- Experience participating in monitor visits, audits, SIVs, and investigator meetings
- Experience using EDC systems and resolving sponsor queries
- On-site clinical research site supporting active clinical trials and patient-facing activities.
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