Unblinded Clinical Research Coordinator I

• Compound and dispense prescribed IP.
• Supervise and maintain records of all medications
• Ensure compliance with study-specific blinding plans.
• Provide consultative support regarding the preparation and dosing of drugs.
• Maintain documentation of IP accountability: receipt, dispensing, return to sponsor/destruction.
• Interpret clinic schedule and protocol into a resource that can be used to identify the date/time to compound/prepare and dispense IP for clinical trials.
• Understand and apply all applicable site procedures.
• Ensure receipt and proper storage of IP and bioretention samples.
• Manage inventory, ensuring that expired items are removed from the inventory prior to expiration, and purchasing, and delivery processes for the pharmacy.
• Review protocols and provide input on clinical and pharmacy supply needs.
• Meet with sponsors, monitors, auditors, and regulatory authorities to review drug accountability and other study-specific information.
• Temperature reporting.
• Any other duties/ tasks assigned by the manager, computer proficiency, especially Word, Excel, Outlook, and Google Docs. 

• High School Diploma or equivalent required 
• Foreign Medical Graduate is a plus
• Pharmacy Technician Certification a plus

• Clinical Experience 

• LPN (Licensed Professional Nurse) or CMA (Certified Medical Assistant)

• Computer proficiency, especially Word, Excel, Outlook, and Google Docs. 
• Excellent communication and customer service skills. 
• Outgoing personality Well-organized with attention to detail. 
• Must be able to multitask. 
• Bilingual (Spanish) preferred but not required