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Clinical Research Jobs in Springfield, MO (NOW HIRING)

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 the drug research field. This position is primarily responsible for monitoring the study volunteers ...

QPS, LLC

Clinical Pharmacist

Springfield, MO · On-site

$111K - $133K/yr

The Job The Clinical Pharmacist works closely with Principal Investigators and Clinical Operations leadership to support the safe and compliant conduct of clinical research studies. This role is ...

QPS

Clinical Pharmacist

Springfield, MO · On-site

$107K - $128K/yr

The Job The Clinical Pharmacist works closely with Principal Investigators and Clinical Operations leadership to support the safe and compliant conduct of clinical research studies. This role is ...

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All JobsClinical Research JobsClinical Research Jobs in Springfield, MO

Clinical Research information

See Springfield, MO salary details

$44.6K

$97.6K

$171.9K

How much do clinical research jobs pay per year?

As of Aug 23, 2026, the average yearly pay for clinical research 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 is clinical research?

Clinical research is a branch of healthcare science that focuses on studying human health and illness through clinical trials and observational studies. It aims to improve medical knowledge by testing new treatments, drugs, medical devices, or interventions in controlled environments. Clinical research professionals design, conduct, and monitor studies to ensure that data is accurate and that participant safety and ethical standards are maintained. The results of clinical research can lead to new therapies, improved patient care, and informed healthcare policies.

What are different clinical research jobs?

Some of the different types of clinical research jobs include clinical research associates, coordinators, data managers, clinical nurses, research scientists, and biostatisticians. There are also administrative, managerial, and recruitment positions. As a research associate, you monitor the clinical trials and the people administering them, such as clinical nurses and research coordinators who work under the direction of the principal investigator. As a biostatistician, your duties are to collect data about the study and analyze the results to determine if the medication or treatment shows statistically significant effects on participants.

What are the key skills and qualifications needed to thrive in clinical research, and why are they important?

To thrive in Clinical Research, you need a strong background in life sciences, data analysis, and regulatory compliance, often supported by a relevant degree and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications like GCP (Good Clinical Practice) are commonly required. Attention to detail, strong organizational skills, and effective communication make candidates stand out in this field. These skills ensure the integrity of research data, regulatory adherence, and successful collaboration among cross-functional teams.

What are some typical challenges faced by professionals in clinical research, and how can they be managed?

Clinical research professionals often face challenges such as strict regulatory compliance, tight timelines, and coordination among multidisciplinary teams. Managing large volumes of data and ensuring participant safety are also key concerns. Staying organized, maintaining open communication with team members, and keeping updated on regulatory changes can help professionals navigate these challenges effectively. It's also helpful to develop strong project management skills and to build collaborative relationships with investigators, sponsors, and regulatory bodies.

What is the difference between Clinical Research vs Clinical Data Coordinator?

AspectClinical ResearchClinical Data Coordinator
Required CredentialsTypically a bachelor's degree in health sciences, life sciences, or related field; certifications like CCR or CCRA are commonOften a bachelor's degree in health or data management; certifications like CDMP or CCRC may be preferred
Work EnvironmentResearch sites, pharmaceutical companies, CROs, hospitalsClinical trial sites, hospitals, research organizations
Job FocusDesigning, managing, and overseeing clinical trialsManaging and ensuring accuracy of clinical trial data

Clinical Research involves overseeing entire clinical trials, including protocol development and compliance, while Clinical Data Coordinators focus on collecting, managing, and ensuring the quality of trial data. Both roles are essential in the clinical research process but differ in scope and responsibilities.

How do you become a clinical researcher?

To become a clinical researcher, typically a bachelor's degree in a health-related field such as biology, nursing, or medicine is required, followed by relevant experience or advanced education like a master's or PhD. Certification in clinical research, such as the Certified Clinical Research Professional (CCRP), can enhance job prospects. Strong analytical skills, knowledge of regulatory guidelines, and familiarity with research tools are also important.

Is clinical research a good career path?

Clinical research is a viable career that involves managing and conducting trials to test new medical treatments and drugs. It requires strong organizational skills, knowledge of regulatory guidelines, and often a background in healthcare or life sciences. The field offers opportunities for advancement and specialization, with roles in research coordination, data management, and regulatory affairs.

What do you do in a clinical research job?

A clinical research job involves designing, conducting, and managing studies to evaluate the safety and effectiveness of medical treatments or devices. Professionals in this field collect and analyze data, ensure compliance with regulatory standards, and often work with clinical trial participants, using tools like electronic data capture systems. Strong attention to detail, knowledge of Good Clinical Practice (GCP), and relevant certifications are important for success.

What qualifications do you need to be a clinical research professional?

A clinical research professional typically needs a bachelor's degree in a health-related field such as biology, nursing, or pharmacy. Relevant certifications, like the Certified Clinical Research Professional (CCRP), and knowledge of Good Clinical Practice (GCP) guidelines are often required. Strong organizational skills and familiarity with clinical trial management systems are also important.
More about Clinical Research jobs

What are the most commonly searched types of Clinical Research jobs in Springfield, MO?

The most popular types of Clinical Research jobs in Springfield, MO are:

What are popular job titles related to Clinical Research jobs in Springfield, MO?

For Clinical Research jobs in Springfield, MO, the most frequently searched job titles are:

What job categories do people searching Clinical Research jobs in Springfield, MO look for?

The top searched job categories for Clinical Research jobs in Springfield, MO are:

What cities near Springfield, MO are hiring for Clinical Research jobs?

Cities near Springfield, MO with the most Clinical Research job openings:

Clinical Research jobs near you
Infographic showing various Clinical Research job openings in Springfield, MO as of August 2026, with employment types broken down into 4% As Needed, 71% Full Time, 17% Part Time, and 8% 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 Assistant

Headlands Research

Springfield, MO • On-site

$18 - $22/hr

Full-time

Medical, Dental, Life, Retirement, PTO

Posted 4 days ago

Job description

Everybody is unique. This means the medicine that works for one person might not work for millions of others- and that's what gets us out of bed every morning. At Clinvest Research, we study chronic, unseeable conditions like migraine, arthritis, and diabetes to help bring new treatment options to the world.

We've been conducting clinical trials in southwest Missouri for more than 30 years and have been a part of over 400 trials in over 20 therapeutic areas. In order to keep growing and helping more patients nd hope in their conditions, we're on the hunt for a team member to join us in our effort as a Clinical Research Assistant.

 

As a Clinical Research Assistant, you'll assist with clinical trial procedures as an integral part of the research team. Your direction will be assigned by the Director of Research, but your day-to-day could take many forms. From hands-on time with patients to driving around Springeld on supply runs or touching up on protocol training, everything you do plays an essential role in advancing tomorrow's medicine- today.

 

We believe in sweating the small stuff-here's a list of responsibilities you can expect to be involved in:

 

  • Assist with laboratory functions such as blood draws, maintaining lab kits, processing lab samples, and shipping labs
  • Perform visit assessments such as weight, blood pressure and ECG
  • Provide administrative support to the research team members
  • Protocol-specic training
  • Communicate effectively and work in collaboration with the research team in order to meet research study objectives
  • Aid in recruitment and phone screening of potential patients utilizing patient database and prospective patient database
  • Comply with institutional and departmental policies and procedures
  • Travel in and around Springeld for supply pickup and specimen drop off
  • Manage the storage and retention of study documents as per outlined in study protocols
  • Prioritize workload, plan, organize, track, and follow up on projects and tasks with the ability to meet deadlines and handle multiple tasks accurately
  • Complete word processing, spreadsheet, and database data entry, including, but not limited to, correspondence, records, reports, scanning, emailing, copying, and other tasks as directed by the study These are done neatly, accurately, and in a timely manner
  • Conduct patient visits, in person and phone call
  • Report punctually in-ofce Monday-Thursday, 08:00am-05:00pm and Friday 8am-12pm
We believe in helping you understand the ne print-here's a list of skills that would make you best t for this position:

 

Skills/Qualications: Reporting skills, administrative writing skills, Microsoft Ofce skills, managing processes, organization, analyzing information, professionalism, problem-solving, verbal and written communication, ability to focus on and perform detailed work, previous phlebotomy skills or willingness to learn phlebotomy, previous ECG experience or willingness to learn.

The hourly rate for this position is $18-$22 and is based on the depth of your skills and prior experience.

We believe in life outside of work

 

Loving your life is the rst step to loving your job. It's part of the equilibrium. We offer paid time off where we encourage you to unplug, take a vacation, and come back fresh and refueled.

As a break from the daily tasks and to-dos, we also nd any reason we can to celebrate. Birthdays, holidays, successes, major life events-get ready to celebrate the people around you!

During the days when the pedal is to the metal in-ofce, we hold schedule exibility on a precious pedestal. In addition, we offer medical, dental, life insurance, and a 401k program with company matching.

We believe in double and triple checks.

 

This is a detail-oriented job, and since you t that requirement, you'll make sure to include #TripleCheck in the subject line of the email you send us with your resume. Bonus points for resumes with references we don't have to ask you for.

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