Onsite Clinical Research Coordinator Mercy STL Full Time

Onsite position

The Clinical Research Coordinator (CRC) is responsible for coordinating clinical research studies conducted through Mercy Research. This role manages the day-to-day operations of clinical trials including patient recruitment study coordination data collection regulatory compliance and communication with sponsors physicians patients and research staff.

The Clinical Research Coordinator ensures studies are conducted according to protocol regulatory requirements and Mercys Mission Values and Service Standards while supporting the advancement of clinical research and patient care.

• Coordinate study activities from start-up through completion.
• Maintain a thorough understanding of assigned protocols and ensure adherence to study requirements.
• 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.
• Build positive relationships with participants while ensuring an exceptional patient experience.

• Collect document and maintain accurate research data and study records.
• Complete source documentation and case report forms in a timely manner.
• Ensure compliance with ICH/GCP guidelines regulatory requirements and institutional policies.
• Support quality assurance and audit activities.

• Serve as a liaison between Mercy Research sponsors CROs physicians and clinical staff.
• Assist with training and mentoring research staff and new team members.
• Support research recruitment initiatives and community outreach efforts.
• Attend investigator meetings and study-related trainings as needed.

• High School Diploma or equivalent.
• Four (4) years of clinical medical biotechnology laboratory 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.

• Bachelors degree in a Health or Science-related field.
• Three or more years of clinical research experience.
• Phlebotomy experience.

• Ability to lift push and pull up to 50 pounds regularly.
• Ability to stand and walk for extended periods throughout the workday.
• Ability to bend kneel squat twist reach and perform repetitive movements as needed.

Join a collaborative team dedicated to improving patient outcomes through innovative clinical research. As a Clinical Research Coordinator youll play a key role in advancing medical discoveries while helping patients gain access to cutting-edge treatments and therapies.