Unblinded Clinical Research Coordinator I

at  DM Clinical Research

UNBLINDED CLINICAL RESEARCH COORDINATOR I

DM Clinical Research is looking to hire an Unblinded Clinical Research Coordinator to join our team. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials.

Duties & Responsibilities:

• 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.

KNOWLEDGE & EXPERIENCE:

Education:

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

Experience:

• Clinical Experience

Credentials:

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

Knowledge and Skills:

• 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

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• 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