Clinical Research Coordinator — IP Dispensing

DM Clinical Research; Philadelphia (Philadelphia County); On-site; USD 50,000 - 70,000; Full time

Job summary

A leading clinical research organization in Philadelphia is looking for an Unblinded Clinical Research Coordinator. This role requires supervising and dispensing Investigational Products (IP) during clinical trials, ensuring compliance with protocols, and maintaining accurate records. Candidates should have a High School Diploma and clinical experience, with credentials as either an LPN or CMA preferred. The position demands strong attention to detail and proficiency in common software applications. This role offers an opportunity to impact clinical trial processes positively.

Qualifications

• High School Diploma or equivalent required.
• Clinical experience is required.
• Licensed Professional Nurse (LPN) or Certified Medical Assistant (CMA) credentials 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 for drug preparation and dosing.
• Maintain documentation of IP accountability.
• Manage inventory of medications.
• Review protocols for clinical and pharmacy supply needs.
• Meet with stakeholders for drug accountability.
• Temperature reporting.

Skills

Computer proficiency (Word, Excel, Outlook, Google Docs)

Excellent communication skills

Customer service skills

Attention to detail

Outgoing personality

Multitasking

Bilingual (Spanish)

Education

High School Diploma or equivalent

Foreign Medical Graduate

Tools

Word

Excel

Outlook

Google Docs

Job description

A leading clinical research organization in Philadelphia is looking for an Unblinded Clinical Research Coordinator. This role requires supervising and dispensing Investigational Products (IP) during clinical trials, ensuring compliance with protocols, and maintaining accurate records. Candidates should have a High School Diploma and clinical experience, with credentials as either an LPN or CMA preferred. The position demands strong attention to detail and proficiency in common software applications. This role offers an opportunity to impact clinical trial processes positively.