Unblinded CRC - Contract - Denver, CO
Drive clinical excellence behind the scenes-join as an Unblinded CRC in Denver and make every dose count.
Proclinical is seeking an Unblinded Clinical Research Coordinator (CRC) to support the daily operations of assigned clinical trials in Denver, CO. This position requires strong organizational skills, attention to detail, and the ability to work both independently and collaboratively.
Primary Responsibilities:
The successful candidate will focus on managing Investigational Products (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 communication skills.
- Local travel may be required for multi-site locations.
The Unblinded CRC's responsibilities will be:
- Communicate study procedures and outcomes to patients or caregivers.
- 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.
- Manage inventory of lab and study supplies, notifying the manager when reordering is necessary.
- Perform protocol-specific procedures such as taking vital signs, conducting electrocardiograms, and collecting laboratory specimens.
- Record and report adverse events and side effects, collaborating with investigators as needed.
- Resolve electronic data queries within 24 hours of issuance by the sponsor.
- Dispense medical devices or drugs, calculate dosages, and provide instructions as required.
- Maintain accurate drug accountability logs, including tracking medication shipments and dispensation.
- Prepare and maintain master logs for each study, including informed consent forms and patient enrollment records.
- Participate in quality assurance audits and ensure proper labeling and organization of drug storage areas.
- Maintain accurate temperature logs for IP storage equipment.
- Attend investigator meetings and site initiation visits.
- Train backup unblinded or pharmacy team members as needed.
- Ensure all required IP documents and equipment are obtained for study conduct.
- Communicate with sponsors regarding IP management and prepare source documents for IP preparation and administration.
- Administer investigational products as per the IP manual and perform unblinded monitor visits.
Compensation:
If you are having difficulty in applying or if you have any questions, please contact Janelle Jones at j.jones@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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