Unblinded Clinical Research Coordinator

DM Clinical Research; Phoenix (AZ); On-site; USD 60,000 - 80,000; Full time

Job summary

A leading clinical research organization in Phoenix, AZ is seeking an Unblinded Clinical Research Coordinator. Responsibilities include compounding and dispensing Investigational Products, supervising medication records, and ensuring compliance in clinical trials. The ideal candidate will have a High School Diploma, clinical experience, and LPN or CMA credentials. Strong communication skills and computer proficiency are essential for this role, which offers the opportunity to work in an important field of clinical research.

Qualifications

• High School Diploma or equivalent is required.
• Clinical experience is necessary.
• Credentials as LPN or CMA are required.

Responsibilities

• Compound and dispense prescribed Investigational Products.
• Supervise and maintain medication records.
• Ensure compliance with study-specific blinding plans.
• Review protocols and provide input on supply needs.

Skills

Computer proficiency

Excellent communication skills

Customer service skills

Attention to detail

Multitasking

Bilingual (Spanish)

Education

High School Diploma or equivalent

Foreign Medical Graduate

Tools

Word

Excel

Outlook

Google Docs

Job description

Position: Unblinded Clinical Research Coordinator

Location: Phoenix, AZ

Job Id: 1153

# of Openings: 3

Unblinded Clinical Research Coordinator

DM Clinical Research, the largest privately‑owned clinical research organization in the Houston area and one of the top fifty in the country, is looking for 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.

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.