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Clinical Research Study Manager Jobs in Springfield, MO

QPS, LLC

PRN Logistics Technician

Springfield, MO · On-site

$18 - $22.50/hr

Prepare, package, and ship study kits, laboratory supplies, and clinical materials in compliance ... Previous experience in logistics, inventory management, laboratory support, or shipping/receiving ...

Myana

Physician-Neurology

Spokane, MO · On-site

$200 - $240/hr

... studies to guide clinical management. * Prescribing appropriate pharmacologic and non-pharmacologic ... research, academic, or administrative position with no patient care responsibilities. The ...

Integrated Resources INC

Lab Tech

Springfield, MO

$17.25 - $23/hr

Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Job Title: Lab ... HPLC, GC, Color Power Communicate out of specification issues to management Returning extra samples ...

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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 Sep 3, 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.

PRN Logistics Technician

QPS, LLC

Springfield, MO • On-site

$18 - $22.50/hr

Other

Posted 22 days ago

Job description

Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Stage Clinical and Phase I IV Clinical Research services. We welcome individuals who want to be part of our growing organization. QPS is an innovative, dynamic organization that strives to employ talented, caring and committed employees who will work collaboratively towards achieving our mission of improving human health and the quality of life. QPS offers challenging and rewarding work in its four core business areas and support functions. Underpinning the operation is a culture that values diversity, innovation and accountability. Employees are encouraged to take responsibility and achieve their best, both as individuals and as team members.


Description:

The Logistics Technician is responsible for supporting daily QPS Logistics operations through inventory management, kit assembly, and shipping coordination. This role requires strong organizational skills, attention to detail, and the ability to work efficiently within multiple computer-based inventory and tracking systems. The Logistics Technician plays a critical role in ensuring study materials, laboratory kits, and supplies are prepared accurately and delivered on schedule. This is a PRN position.


Responsibilities:

  • Read and understand the guidelines of the study protocols and laboratory manuals.
  • Maintain and update inventory records using Excel and various inventory management platforms
  • Monitor inventory levels and assist with ordering laboratory and operational supplies 
  • Assemble laboratory kits and study kits according to protocol-specific instructions and quality requirements 
  • Prepare, package, and ship study kits, laboratory supplies, and clinical materials in compliance with company procedures and shipping regulations 
  • Process incoming and outgoing shipments and maintain accurate shipping documentation 
  • Coordinate and communicate through email with internal departments, vendors, and study teams regarding logistics activities 
  • Verify accuracy of kit components, labeling, and shipment contents prior to distribution 
  • Organize and maintain storage areas to ensure inventory accuracy and operational efficiency 
  • Assist with tracking lot numbers, expiration dates, and inventory reconciliation activities 
  • Support study startup and ongoing study logistics requirements as assigned 
  • Maintain accurate records and documentation in accordance with company standards and regulatory requirements 
  • Perform additional logistics and operational support duties as needed

QUALIFICATIONS:

  • Combination of relevant education & experience that provides sufficient knowledge & skills to ensure incumbent’s success in this role, such as: 
    • High school diploma or equivalent, with some experience in an environment requiring confidentiality, discretion, and attention to detail
    • Previous experience in logistics, inventory management, laboratory support, or shipping/receiving preferred
  • Experience in a Regulated industry laboratory preferred 
  • Proficiency in Microsoft Excel and general computer applications
  • Minimum of 1 year experience working in a fast paced, detail-oriented environment preferred

 

EEO Minorities/Females/Protected Veterans/Disabled

QPS is an equal opportunity employer. In accordance with anti-discrimination law, it is the purpose of this policy to effectuate these principles and mandates. QPS prohibits discrimination and harassment of any type and affords equal employment opportunities to employees and applicants without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law. QPS conforms to the spirit as well as to the letter of all applicable laws and regulations.