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Clinical Research Monitor Auditor Jobs (NOW HIRING)

PRISM Vision Group

Clinical Research Nurse

Hampton, VA · On-site

$47K - $128K/yr

Clinical Research RN Opportunity Virginia Oncology Associates, the largest group of medical ... Participates in scheduling monitoring and auditing visits, as well as interacting with the monitors ...

PRISM Vision Group

Clinical Research Coordinator

Salem, VA · On-site

$19.62 - $30.18/hr

Clinical Research Coordinator Responsible for supporting the management and coordination of tasks ... May participate in scheduling monitoring and auditing visits, as well as interact with the monitors ...

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How much do clinical research monitor auditor jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for clinical research monitor auditor in the United States is $38.70, according to ZipRecruiter salary data. Most workers in this role earn between $38.22 and $39.18 per hour, depending on experience, location, and employer.

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Infographic showing various Clinical Research Monitor Auditor job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 18% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $80,500 per year, or $38.7 per hour.

Unblinded Clinical Research Coordinator

Detroit, MI

DM Clinical Research
11 - 50 employees
Learn more about DM Clinical Researchexternal

$24 - $32/hr

Full-time

Re-posted 16 days ago

Job description

Unblinded Clinical Research Coordinator
DM Clinical Research 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 amp; 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 amp; 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

Apply