Clinical Pharmacist - Trials & Regulatory Support

QPS Holdings, LLC; Springfield (MO); On-site; USD 110,000 - 140,000; Full time

Job summary

QPS Holdings, LLC is seeking a Clinical Pharmacist to join our team in Missouri. The role involves ensuring proper handling of investigational products, supporting pharmacy operations, and maintaining regulatory compliance across clinical trials.

You will collaborate with Principal Investigators and Operations leadership to execute trials, monitor events, and assist with audits and sponsor visits, contributing to patient safety and study integrity.

Qualifications

• State-Registered Pharmacist licensure required.
• Clinical research experience helpful.
• Strong understanding of FDA/GCP/ICH guidelines.
• Experience in hospital, clinical, or research pharmacy environments helpful.
• Strong communication, organizational, and problem-solving skills; good monitoring and documentation skills needed.

Responsibilities

• Oversee receipt, storage, dispensing, accountability, and documentation of study medications.
• Maintain investigational product inventory and ensure protocol/regulatory compliance.
• Monitor and document medication-related events and communicate with the study team.
• Support occasional compounding activities per study requirements and standards.
• Train and support research staff on study-specific pharmacy procedures.
• Participate in sponsor visits, monitoring visits, and audits.
• Collaborate with clinical operations, investigators, and study teams to support trial execution.

Skills

State-licensed pharmacist

Clinical research experience

FDA/GCP/ICH guidelines

Communication

Organizational skills

Problem-solving

Documentation skills

Job description

QPS Holdings, LLC is seeking a Clinical Pharmacist to join our team in Missouri. The role involves ensuring proper handling of investigational products, supporting pharmacy operations, and maintaining regulatory compliance across clinical trials.

You will collaborate with Principal Investigators and Operations leadership to execute trials, monitor events, and assist with audits and sponsor visits, contributing to patient safety and study integrity.