Clinical Research Coordinator

• Saint Louis, Missouri
• Support Services
• Research
• Regular
• Full-time
• Mercy Hospital St Louis
• JR227937

Find Your Calling At Mercy

The Clinical Research Coordinator (CRC) is responsible for coordination of research studies conducted by Mercy Research. The Clinical Research Coordinator is responsible for the day-to-day operational tasks related to clinical trials and performs a variety of duties including, but not limited to: volunteer recruitment, drug/device/supply inventory maintenance, interaction with physicians, nurses, office staff, patients, and clinical monitors. Duties also include the collection, compilation, documentation and analysis of clinical research data while following local, state and federal regulations. The Clinical Research Coordinator will assist in training and preceptor duties. The study load and complexity will increase from the Associate Clinical Research Coordinator responsibility, thereby increasing the overall number of enrollments and visits. The Clinical Research Coordinator will assist with communication and relationship building with sponsors and CROs.

Performs duties and responsibilities in a manner consistent with our mission, values, and Mercy Service Standards.

Position Details:
Clinical Research Coordinator

Location: Mercy St. Louis

Schedule: Full-Time

Overview:

Mercy Research is seeking a Clinical Research Coordinator (CRC) to join our team. In this role, you will manage the coordination and execution of clinical research studies, ensuring compliance with all regulatory requirements. The CRC is responsible for day-to-day operations of clinical trials, including patient recruitment, data collection, and collaboration with physicians, nurses, office staff, and clinical monitors. You will also maintain study supplies, oversee documentation, and support training initiatives.

This position involves a higher level of complexity and study load compared to an Associate CRC, with increased patient enrollments and visits. Additionally, you will assist in building strong relationships with sponsors and CROs.

Key Responsibilities:

1. Study Preparation & Protocol Compliance

• Complete pre-study checklists and feasibility questionnaires accurately and on time.
• Maintain thorough knowledge of assigned protocols and trial structures.
• Ensure adherence to all regulatory and institutional research requirements.

2. Patient Engagement & Safety

• Conduct patient screening, consent, and education.
• Monitor patient safety through interviews, diagnostics, and drug safety assessments.
• Schedule and manage patient visits efficiently.

3. Data Management & Documentation

• Update case report forms and source documents promptly and accurately.
• Collect and prepare lab specimens; maintain inventory of trial supplies.
• Participate in quality control and compliance monitoring.

4. Team Collaboration & Training

• Assist in training new and current staff on protocol-specific duties.
• Support research assistants, clerical staff, and volunteers.
• Foster a collaborative and efficient research environment.

Minimum Qualifications:

• Education: High School Diploma or equivalent.
• Experience: 4 years in clinical, medical, or biotech lab settings OR equivalent combination of education and experience.
• Skills:
• Knowledge of ICH/GCP guidelines and regulatory requirements.
• Strong verbal/written communication and critical thinking skills.
• Familiarity with medical terminology and electronic medical records.
• Ability to manage multiple projects independently with attention to detail.
• Proficiency in Microsoft Office and database applications.

Preferred Qualifications:

• Education: Bachelor's degree in health or science field.
• Experience: 3+ years in clinical research; phlebotomy experience.

Physical Requirements:

• Ability to push, pull, and lift up to 50 lbs regularly.
• Prolonged standing and walking during shifts.
• Ability to bend, kneel, twist, and squat as needed.

Why Mercy?

From day one, Mercy offers outstanding benefits - including medical, dental, and vision coverage, paid time off, tuition support, and matched retirement plans for team members working 32+ hours per pay period.

Join a caring, collaborative team where your voice matters. At Mercy, you'll help shape the future of healthcare through innovation, technology, and compassion. As we grow, you'll grow with us.

---