Unblinded Clinical Research Coordinator - Contract - Moore, OK
Where impeccable IP management meets flawless trial execution.
Proclinical is seeking an Unblinded Clinical Research Coordinator to support the daily operations of assigned clinical trials. This position requires strong organizational skills, attention to detail, and the ability to work collaboratively with site managers and study participants.
Primary Responsibilities:
The successful candidate will focus on managing Investigational Product (IP) for clinical research trials, ensuring compliance with protocols, and maintaining the integrity of blinded and unblinded staff roles.
Skills & Requirements:
- Experience in clinical research is preferred.
- High school diploma or GED required; some college coursework is preferred.
- Strong ability to work independently and collaboratively as part of a team.
- Excellent organizational and problem-solving skills.
- Local travel may be required for multi-site locations.
The Unblinded Clinical Research Coordinator's responsibilities will be:
- Communicate with site managers and study participants regarding study details.
- Manage all aspects of Investigational Product (IP), including receipt, storage, dispensing, destruction, return, and administration.
- Maintain accurate IP accountability and ensure compliance with study protocols.
- Monitor study activities to ensure adherence to regulatory and institutional policies.
- Complete and maintain source documentation and enter data into EDC systems within specified timeframes.
- Perform protocol-specific procedures such as taking vital signs, conducting electrocardiograms, and collecting laboratory specimens.
- Record and report adverse events and side effects, resolving queries promptly.
- Dispense medical devices or drugs, calculate dosages, and provide instructions as needed.
- Inventory and manage lab and study supplies, notifying management when replenishment is required.
- Prepare the site for study conduct, including training backup team members and ensuring all required IP documents and equipment are in place.
- Attend investigator meetings and site initiation visits.
- Participate in quality assurance audits and maintain accurate temperature logs for IP storage.
If you are having difficulty in applying or if you have any questions, please contact Jackie Cerchio at j.cerchio@proclinical.com
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
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