Unblinded Clinical Research Coordinator - Edmond, OK

Unblinded Clinical Research Coordinator - Contract - Edmond, OK

Ready to be the heartbeat of clinical research? Join our client and assist in turning innovative science into life-changing care!

Proclinical is seeking an Unblinded Clinical Research Coordinator to support the daily operations of clinical trials.

In this role, you will focus on managing Investigational Products (IP), ensuring compliance with study protocols, and maintaining the integrity of blinded and unblinded staff roles. This position requires attention to detail, strong organizational skills, and the ability to work both independently and collaboratively.

• Experience in clinical research is preferred.
• High school diploma or GED required; some college coursework is preferred.
• Strong organizational and problem-solving skills.
• Ability to work independently and collaboratively as part of a team.
• Local travel may be required for multi-site locations.

• Communicate with site managers and study participants regarding study-related information.
• Ensure adherence to site Standard Operating Procedures (SOPs).
• Manage all aspects of Investigational Product (IP), including receipt, storage, dispensing, destruction, return, and administration.
• Maintain the blind for studies requiring separate blinded and unblinded staff roles.
• Monitor study activities to ensure compliance with protocols and regulatory requirements.
• Complete and maintain accurate source documentation during patient visits and enter data into the Electronic Data Capture (EDC) system within 48 hours.
• Inventory lab and study supplies, notifying the manager when replenishment is needed.
• Perform protocol-specific procedures such as patient interviews, vital signs, electrocardiograms, and laboratory specimen collection.
• Record and report adverse events and side effects, resolving queries within 24 hours.
• Dispense medical devices or drugs, calculate dosages, and provide necessary instructions.
• Log and maintain accurate records of drug accountability, including medication shipments and dispensation.
• Prepare and maintain master logs for each study, including informed consent forms and patient enrollment.
• Participate in quality assurance audits and ensure proper labeling and organization of drug storage areas.
• Maintain accurate temperature logs for IP storage equipment.
• Train backup unblinded team members and ensure all required IP documents and equipment are available.
• Communicate with sponsors and unblinded monitors regarding IP management and conduct unblinded monitor visits.

• $20 to $25 per hour