Principal Investigator, Clinical Trials (Part-Time)

Eximia Research; St. Louis (MO); On-site; USD 83,000 - 124,000; Part time

Job summary

Eximia Research seeks a Research Investigator to oversee clinical safety and data collection for ongoing trials in Missouri. The role supports coordinators, PIs, and staff while ensuring patient well-being. Part-time up to 10 hours weekly.

Responsibilities include leading study teams, training staff, coordinating trial activities, ensuring data integrity, and maintaining regulatory compliance with GCP/ICH and SOPs.

Qualifications

• Must be licensed as an NP, PA, MD, or DO in the state of Missouri.
• Ability to communicate effectively in English (oral and written).
• Willingness to travel up to 10% for meetings and conferences.

Responsibilities

• Lead a study team to execute clinical trials.
• Mentor and train staff on trial conduct and protocol requirements.
• Develop training strategies and mitigation plans for trials.
• Conduct and manage trials per protocol, GCP, ICH, and SOPs.
• Coordinate start-up, vendor management, subject recruitment, data entry, and query resolution.
• Ensure data confidentiality and good documentation practices.
• Prepare regulatory documents and submissions to Sponsors and IRBs.

Skills

English communication

Job description

Eximia Research seeks a Research Investigator to oversee clinical safety and data collection for ongoing trials in Missouri. The role supports coordinators, PIs, and staff while ensuring patient well-being. Part-time up to 10 hours weekly.

Responsibilities include leading study teams, training staff, coordinating trial activities, ensuring data integrity, and maintaining regulatory compliance with GCP/ICH and SOPs.