Clinical Research Coordinator (CRC)

About the role

This role is a unique opportunity for a Clinical Research Coordinator who is excited by the idea of helping build and grow one of our newer sites located in Springfield, MO. Starting as a part-time opportunity, this position has strong potential to transition into a full-time role as trial activity and patient volume continue to expand. This opportunity is expected to average approximately 24–30 hours per week and offers a flexible mix of remote and on-site responsibilities based on clinical trial activity and site needs.

Key Responsibilities

• Conduct and coordinate all aspects of clinical trial activities at the site
• Perform phlebotomy on patients, following proper clinical and safety protocols
• Recruit, screen, and enroll study participants according to inclusion/exclusion criteria
• Schedule and conduct study visits, ensuring adherence to protocol requirements
• Accurately collect, process, and ship biological samples per study-specific guidelines
• Complete and maintain study documentation, including source documents, regulatory binders, and informed consent forms
• Perform timely and accurate data entry into electronic data capture systems (EDC)
• Communicate effectively with sponsors, monitors, and other research team members
• Ensure compliance with GCP, ICH, FDA, and IRB regulations
• Assist in monitoring visits and audit preparation as needed

Qualifications

• Minimum of 1–2 years of experience as a Clinical Research Coordinator, in a similar environment
• Phlebotomy certification or demonstrated competency in venipuncture (pediatric and adult required)
• Strong understanding of clinical trial operations, regulatory documentation, and data management
• Excellent attention to detail, organization, and time management skills
• Strong interpersonal and communication abilities with patients and clinical staff
• Proficient in Microsoft Office and electronic data capture systems
• CPR certification preferred

Benefits

We are committed to providing a supportive and inclusive work environment. Our benefits package includes:

• Competitive compensation
• Flexible schedule
• Professional development opportunities
• Health and wellness programs
• Employee recognition and rewards

Pay

The pay range for this position is $25 - $30 per hour, depending on experience and qualifications.

Schedule

This role is expected to average approximately 24–30 hours per week and offers a flexible mix of remote and on-site responsibilities based on clinical trial activity and site needs.

Skills

To succeed in this role, you should have:

• Strong organizational and time management skills
• Excellent communication and interpersonal skills
• Ability to work independently and as part of a team
• Attention to detail and accuracy in data entry
• Knowledge of clinical trial operations and regulatory requirements

Benefits

We offer a comprehensive benefits package that includes:

• Health insurance
• Dental insurance
• Vision insurance
• Retirement savings plan
• Flexible spending accounts
• Life insurance
• Short-term disability coverage
• Long-term disability coverage
• Employee assistance program
• Generous paid time off

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