Unblinded Clinical Research Coordinator - 244137 Job at Medix™, Moore, OK

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  • Medix™
  • Moore, OK

Job Description

Job Title: Unblinded Clinical Research Coordinator

Location: Moore, Ok

Pay Range: Up to $25 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

Preferred Qualifications:

  • 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

Work Environment:

  • On-site clinical research site supporting active clinical trials and patient-facing activities.

Job Tags

Hourly pay, Permanent employment, Full time, Contract work, Immediate start, Monday to Friday,

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