IP Clinical Research Coordinator I — Unblinded

DM Clinical Research; Philadelphia (Philadelphia County); On-site; USD 42,000 - 64,000; Full time

Job summary

DM Clinical Research in Philadelphia seeks an Unblinded Clinical Research Coordinator I to join our team. The role involves compounding and dispensing Investigational Products (IP), maintaining medication records, and ensuring adherence to blinding plans.

Responsibilities include IP accountability documentation, inventory management, and collaboration with sponsors, monitors, and regulatory authorities. Strong communication and multitasking skills are essential.

Qualifications

• High School Diploma or equivalent required.
• Foreign Medical Graduate is a plus.
• Pharmacy Technician Certification is a plus.
• LPN or CMA credentials are preferred.

Responsibilities

• Compound and dispense prescribed Investigational Products (IP).
• Supervise and maintain records of all medications.
• Ensure compliance with study-specific blinding plans.
• Provide consultative support on preparation and dosing of drugs.
• Maintain IP accountability documentation: receipt, dispensing, and destruction.
• Interpret clinic schedule and protocol to plan IP dispensing.
• Manage inventory and expiration, and handle purchasing and delivery for the pharmacy.
• Meet with sponsors, monitors, auditors, and regulatory authorities.
• Record temperature data as required.
• Perform other duties assigned by supervisor.

Skills

Excellent communication

Customer service

Multitask

Attention to detail

Outgoing personality

Bilingual (Spanish)

Education

High School Diploma or equivalent

Foreign Medical Graduate

Pharmacy Technician Certification

LPN/CMA credentials

Tools

Word

Excel

Outlook

Google Docs

Job description

DM Clinical Research in Philadelphia seeks an Unblinded Clinical Research Coordinator I to join our team. The role involves compounding and dispensing Investigational Products (IP), maintaining medication records, and ensuring adherence to blinding plans.

Responsibilities include IP accountability documentation, inventory management, and collaboration with sponsors, monitors, and regulatory authorities. Strong communication and multitasking skills are essential.