Top 4 Clinical research assistant Jobs in Springfield, Mo

Clinical Research Coordinator (CRC)
Hawthorne Health —Springfield, MO
- $25 - $35 an hour
- Part-time
- Hybrid work
- CPR Certification
- Inventory management
- Mid-level
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Clinical Trial Recruiter
QPS, LLC —Springfield, MO
- Full-time
- Office
- High school diploma or GED
- Recruiting
- Paid holidays
- Disability insurance
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Clinical Research Coordinator (CRC)

Hawthorne Health
Springfield, MO

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Job Details

Part-time
$25 - $35 an hour

Qualifications

Project team coordination
Vascular access
Direct patient care
CPR Certification
Certified Phlebotomy Technician
Regulatory documents
Project documentation
Inventory management
Operations coordination
Phlebotomy specimen handling
Mid-level
Research project coordination
Schedule management
ICH guidelines
Clinical data entry
Informed consent procedures implementation
Organizational skills
Biological sampling
Implementing research protocols
Patient recruitment
Clinical research inspection readiness
Patient interaction
Productivity software
Clinical quality assurance standards
1 year
Communication skills
Project stakeholder communication
Safety protocol implementation
Quality data entry
FDA regulations

Full Job Description

About Us

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/

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