Onsite Clinical Research Coordinator - Impactful Trials

Mercy Hospital St. Louis Critical Care Medicine Fellowship; St. Louis (MO); On-site; USD 42,000 - 64,000; Full time

Benefits offered by this job

Medical, dental, and vision coverage

Paid time off

Tuition support

Matched retirement plans

Job summary

Mercy Research in St. Louis, MO is seeking a Clinical Research Coordinator to manage day-to-day operations of clinical trials, including participant recruitment, study coordination, data collection, regulatory compliance, and sponsor communication.

This onsite role supports Mercy's mission, adheres to ICH/GCP guidelines, and offers opportunities to mentor staff and contribute to innovative patient care. Strong organizational and communication skills are essential; Bachelor's preferred.

Qualifications

• High School Diploma or equivalent.
• Four years of clinical, medical, biotechnology, or related experience.
• Knowledge of ICH/GCP guidelines and clinical research regulations.
• Familiarity with medical terminology and electronic medical records (EMR).
• Strong organizational, communication, and critical thinking skills.
• Ability to manage multiple priorities independently.

Responsibilities

• Coordinate study activities from start-up through completion.
• Schedule and manage participant visits and study procedures.
• Maintain study supplies, equipment, and investigational product inventories.
• Screen, enroll, consent, and educate research participants.
• Monitor participant safety and report adverse events or protocol concerns.
• Collect, document, and maintain accurate research data and study records.
• Serve as a liaison between Mercy Research, sponsors, CROs, physicians, and clinical staff.
• Assist with training and mentoring research staff and new team members.

Skills

ICH/GCP knowledge

EMR familiarity

Strong organizational skills

Communication skills

Multitasking ability

Education

Bachelor's degree in Health or Science-related field

Job description

Mercy Research in St. Louis, MO is seeking a Clinical Research Coordinator to manage day-to-day operations of clinical trials, including participant recruitment, study coordination, data collection, regulatory compliance, and sponsor communication.

This onsite role supports Mercy's mission, adheres to ICH/GCP guidelines, and offers opportunities to mentor staff and contribute to innovative patient care. Strong organizational and communication skills are essential; Bachelor's preferred.