Clinical Research Coordinator (CRC)

Hawthorne Health, Inc.; Springfield (MO); Hybrid; USD 34,000 - 48,000; Part time

Job summary

Hawthorne Health, Inc. seeks a Clinical Research Coordinator for our Springfield, MO site. This role starts as a part-time position (~24–30 hours/week) with potential to transition to full-time as trial activity grows.

You will serve as the site’s operational lead for day-to-day trial activities, with support from an experienced centralized team across recruitment, regulatory, quality, project management, and clinical operations.

Qualifications

• 1–2 years of Clinical Research Coordinator experience in a similar setting.
• Phlebotomy certification or demonstrated competency in venipuncture (adult and pediatric).
• Strong understanding of trial operations, regulatory documentation, and data management.

Responsibilities

• Coordinate all site clinical trial activities.
• Recruit, screen, and enroll participants per criteria.
• Schedule study visits and ensure protocol adherence.
• Collect, process, and ship samples per guidelines.
• Maintain source documents, regulatory binders and informed consent forms.
• Enter data into EDC systems accurately.
• Communicate with sponsors, monitors and team members.
• Ensure compliance with GCP, ICH, FDA and IRB.

Skills

Phlebotomy

Attention to detail

Interpersonal communication

Microsoft Office

EDC systems

Tools

EDC systems

Microsoft Office

Job description

Hawthorne Health is a leading community site network and home research visit solution provider, with 20+ sites and more than 2,000 research experienced healthcare professionals across the U.S. Hawthorne leverages convenient, trusted, healthcare locations, identified patient data, and intelligent technology to accelerate patient access, improve retention, and reduce study costs. By embedding high-quality research within local communities, Hawthorne makes clinical trials more accessible and convenient for patients. Our community-based model shortens timelines and helps bring better treatments to market, faster.

About The Position

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.

We’re looking for someone who is passionate, adaptable, and eager to make a direct impact on the site’s success and long-term growth. As the primary CRC and operational lead for the site, this individual will play a key role in overseeing and coordinating day-to-day clinical trial activities, including investigator coordination, sponsor communication, patient flow, study inventory, regulatory support, and overall site operations.

While this role offers strong ownership and leadership opportunities at the site level, you’ll also be supported by an experienced centralized operations team with expertise across patient recruitment, regulatory, quality, project management, and clinical operations to help ensure the site’s continued success and growth.

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

Hawthorne Health is transforming the clinical trial landscape through an innovative site model that integrates research into community-based settings like local pharmacies. By meeting patients where they already receive care, we are improving access, strengthening trust, and driving more inclusive and efficient trials.

We welcome the opportunity to connect with individuals interested in being part of this evolving model.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us. To view our privacy policy and terms of use, please use the links below. Privacy Policy: https://hawthornehealth.com/privacy-policy/ Terms of Use: https://hawthornehealth.com/terms-of-use/