Clinical Research Coordinator — Mentorship & Global Trials

QPS Holdings, LLC; Springfield (MO); On-site; USD 55,000 - 75,000; Full time

Job summary

QPS is seeking a Clinical Research Coordinator in Springfield, MO to manage pharmaceutical clinical trials from screening to completion. The role requires coordinating visits, ensuring protocol adherence, and maintaining high-quality documentation.

You will interact with sponsors and participants, ensuring study integrity and regulatory compliance. The ideal candidate will have 3 years of experience as a study coordinator, familiarity with GCP, IRB processes, and drug accountability, plus strong

Qualifications

• Ability to coordinate clinical trials from screening through study completion.
• Excellent communication with clients and participants.
• Strong organizational skills and attention to regulatory details.

Responsibilities

• Coordinate the trial from phone screening through study completion with adherence to procedures.
• Attend investigator's meetings, pre-study visits, initiation visits, and monitor-related visits.
• Schedule procedures to maintain study integrity and ensure participant safety and compliance.
• Mentor and train new coordinators and assistants; prepare study documents for archiving.

Skills

Interpersonal skills

Attention to detail

Communication skills

Tools

IRB submission knowledge

Drug accountability procedures

GCP knowledge

Job description

QPS is seeking a Clinical Research Coordinator in Springfield, MO to manage pharmaceutical clinical trials from screening to completion. The role requires coordinating visits, ensuring protocol adherence, and maintaining high-quality documentation.

You will interact with sponsors and participants, ensuring study integrity and regulatory compliance. The ideal candidate will have 3 years of experience as a study coordinator, familiarity with GCP, IRB processes, and drug accountability, plus strong