Unblinded Clinical Research Coordinator I (4513)

Dm Clinical Research Group; Philadelphia (Philadelphia County); On-site; USD 52,000 - 75,000; Full time

Job summary

DM Clinical Research in Philadelphia, PA is seeking an Unblinded Clinical Research Coordinator to join our team. The role includes compounding and dispensing IP, maintaining medication records, and ensuring compliance with blinding plans.

Responsibilities cover IP accountability, scheduling interpretation, and collaboration with sponsors and auditors. Strong organizational and communication skills, plus bilingual Spanish, are valued.

Qualifications

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

Responsibilities

• Compound and dispense prescribed IP.
• Supervise and maintain records of all medications.
• Ensure compliance with study-specific blinding plans.
• Provide consultative support regarding preparation and dosing of drugs.
• Maintain documentation of IP accountability and storage.
• Interpret clinic schedule and protocol for compound/dispense activities.
• Ensure receipt and proper storage of IP and bioretention samples.
• Manage inventory, expiration checks, purchasing and deliveries.
• Review protocols and provide input on supply needs.
• Meet with sponsors, monitors, auditors, and regulatory authorities.

Skills

Excellent communication

Customer service

Organized

multitask

Bilingual (Spanish)

Education

High School Diploma or equivalent

Foreign Medical Graduate

Pharmacy Technician Certification

LPN or CMA credentials

Tools

Microsoft Word

Excel

Outlook

Google Docs

Job description

Job Details: Job Location: Philadelphia - Philadelphia, PA 19107, DM Clinical Research is looking to hire anUnblinded Clinical Research Coordinator Ito join our team.

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