ZipRecruiter

Log In

1

Clinical Research Study Manager Jobs in Springfield, MO

QPS, LLC

Clinical Research Technician

Springfield, MO · On-site

$17 - $23.25/hr

The Clinical Research Technician position offers flexible hours and a rewarding work environment in ... This position is primarily responsible for monitoring the study volunteers and ensuring the ...

QPS

Clinical Pharmacist

Springfield, MO · On-site

$107K - $128K/yr

This position also supports pharmacy operations through inventory management, study drug tracking ... Clinical research experience preferred. * Experience in a hospital, clinical, or research pharmacy ...

QPS, LLC

Clinical Pharmacist

Springfield, MO · On-site

$111K - $133K/yr

This position also supports pharmacy operations through inventory management, study drug tracking ... Clinical research experience preferred. * Experience in a hospital, clinical, or research pharmacy ...

QPS, LLC

Clinical Pharmacist

Springfield, MO · On-site

$111K - $133K/yr

This position also supports pharmacy operations through inventory management, study drug tracking ... Clinical research experience preferred. * Experience in a hospital, clinical, or research pharmacy ...

ProTouch Staffing

Pulmonology Physician

Springfield, MO

$272K - $363K/yr

Competitive 1099 compensation with additional income potential. * ️ Dedicated Clinical Research Coordinators manage daily study operations. * Full regulatory, IRB, and sponsor support provided.

QPS, LLC

Sample Specialist

Springfield, MO · On-site

... clinical research subjects in a timed structure. · Prepare and label study sample tubes. · Ensures all procedures and techniques used follow internal standard operating procedures, clinical ...

next page

Showing results 1-20

All JobsClinical Research Study JobsClinical Research Study Manager JobsClinical Research Study Manager Jobs in Springfield, MO

Clinical Research Study Manager information

See Springfield, MO salary details

$44.6K

$97.6K

$171.9K

How much do clinical research study manager jobs pay per year?

As of Aug 6, 2026, the average yearly pay for clinical research study manager in Springfield, MO is $97,636.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,700.00 and $111,400.00 per year, depending on experience, location, and employer.

What does a clinical research study manager do?

A Clinical Research Study Manager oversees the planning, execution, and completion of clinical trials to ensure they are conducted ethically and in compliance with regulatory standards. They coordinate with research teams, manage budgets and timelines, and ensure accurate data collection and reporting. Their role is crucial in ensuring that clinical studies run smoothly and produce reliable results that can be used for regulatory submissions or scientific publications.

What are the key skills and qualifications needed to thrive as a clinical research study manager?

To thrive as a Clinical Research Study Manager, you need expertise in clinical trial management, regulatory compliance, and protocol development, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications such as GCP (Good Clinical Practice) are typically required. Strong organizational, leadership, and communication skills help manage cross-functional teams and ensure smooth study execution. These skills and qualifications are crucial for maintaining study integrity, meeting regulatory standards, and delivering successful clinical trial outcomes.

What are some common challenges faced by clinical research study managers in coordinating multi-site studies?

Clinical Research Study Managers often encounter challenges in ensuring consistent protocol adherence and data integrity across multiple study sites. Coordinating communication between site teams, managing timelines, and troubleshooting unexpected issues such as recruitment delays or regulatory hurdles are frequent tasks. Successful managers use strong organizational skills and proactive planning to mitigate these challenges, and often rely on regular meetings and digital tools to keep all stakeholders aligned. Establishing clear processes and fostering open communication are key to overcoming these complexities and ensuring study success.

What is the difference between Clinical Research Study Manager vs Clinical Research Coordinator?

AspectClinical Research Study ManagerClinical Research Coordinator
CredentialsBachelor's degree, often with experience in project managementBachelor's degree in health sciences or related field, certification optional
Work EnvironmentOversees multiple studies, manages teams, and coordinates with sponsorsHandles daily study activities, patient interactions, and data collection
Employer & IndustryPharmaceutical companies, CROs, academic institutionsHospitals, clinics, research sites
Search & Comparison IntentUnderstanding managerial roles, responsibilities, and qualificationsFocus on operational tasks and patient management

The Clinical Research Study Manager typically oversees multiple studies, manages teams, and liaises with sponsors, requiring project management skills. In contrast, the Clinical Research Coordinator handles daily study activities, patient interactions, and data collection at research sites. Both roles are essential in clinical research but differ in scope and responsibilities.

What are popular job titles related to Clinical Research Study Manager jobs in Springfield, MO? For Clinical Research Study Manager jobs in Springfield, MO, the most frequently searched job titles are:
What job categories do people searching Clinical Research Study Manager jobs in Springfield, MO look for? The top searched job categories for Clinical Research Study Manager jobs in Springfield, MO are:
What cities near Springfield, MO are hiring for Clinical Research Study Manager jobs? Cities near Springfield, MO with the most Clinical Research Study Manager job openings:
Clinical Research Study Manager jobs near you
Infographic showing various Clinical Research Study Manager job openings in Springfield, MO as of June 2026, with employment types broken down into 2% As Needed, 76% Full Time, 20% Part Time, 1% Temporary, and 1% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $97,636 per year, or $46.9 per hour.

Clinical Research Coordinator (CRC)

Hawthorne Health

Springfield, MO • On-site

$25 - $35/hr

Part-time

Re-posted 3 days ago

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.

$25 - $35 an hour
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/

Apply