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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.
Job Responsibility:
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
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