Unblinded Clinical Research Coordinator I

DM CLINICAL RESEARCH GROUP•Philadelphia, PA

10d•Onsite

About The Position

DM Clinical Research is hiring an Unblinded Clinical Research Coordinator I to support clinical research trials by dispensing investigational products (IP). The role includes preparing and compounding prescribed IP, maintaining medication and accountability records, and ensuring compliance with study-specific blinding plans and site procedures. The coordinator also supports drug preparation and dosing, manages IP storage and inventory, and helps ensure pharmacy supplies meet study needs. The position requires communication with sponsors, monitors, auditors, and regulatory authorities regarding drug accountability and study-specific information. Other duties may be assigned by the manager. Computer proficiency, particularly with Word, Excel, Outlook, and Google Docs, is required.

Requirements

High school diploma or equivalent.
Clinical experience.
LPN (Licensed Professional Nurse) or CMA (Certified Medical Assistant) credential.
Computer proficiency, especially with Word, Excel, Outlook, and Google Docs.
Excellent communication and customer service skills.
Well-organized, with attention to detail.
Ability to multitask.

Nice To Haves

Foreign medical graduate.
Pharmacy Technician Certification.
Bilingual Spanish.

Responsibilities

Compound and dispense prescribed investigational products (IP).
Supervise medications and maintain medication records.
Ensure compliance with study-specific blinding plans.
Provide consultative support regarding drug preparation and dosing.
Document IP accountability, including receipt, dispensing, return to sponsor, and destruction.
Interpret clinic schedules and protocols to determine when IP must be compounded, prepared, and dispensed for clinical trials.
Understand and apply applicable site procedures.
Ensure receipt and proper storage of IP and bioretention samples.
Manage inventory, remove expired items before expiration, and support pharmacy purchasing and delivery processes.
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.
Perform temperature reporting.
Perform other duties or tasks assigned by the manager.