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Clinical Data Management Jobs in Springfield, MO

Brightli

Clinician

Nixa, MO · On-site

$48K - $63K/yr

The Program Coordinator supervises a team of clinical providers, managing team member performance ... Is responsive and cooperative with management needs/requests, such as data collection, program ...

Brightlitalent

Clinician

Nixa, MO · On-site

$48K - $63K/yr

The Program Coordinator supervises a team of clinical providers, managing team member performance ... Is responsive and cooperative with management needs/requests, such as data collection, program ...

Brightli

Clinician

Nixa, MO · On-site

$48K - $63K/yr

The Program Coordinator supervises a team of clinical providers, managing team member performance ... Is responsive and cooperative with management needs/requests, such as data collection, program ...

Brightli

Clinician

Nixa, MO · On-site

$48K - $63K/yr

The Program Coordinator supervises a team of clinical providers, managing team member performance ... Is responsive and cooperative with management needs/requests, such as data collection, program ...

Alps Pharmacy

PRN NURSE PRACTITIONER

Nixa, MO · On-site

Knowledge of computer-based data management programs and information systems, as well as medical ... Demonstrates knowledge of and application of Key Clinical Quality Indicators, and proactively ...

Alps Pharmacy

PRN Nurse Practitioner

Nixa, MO · On-site

Knowledge of computer-based data management programs and information systems, as well as medical ... Demonstrates knowledge of and application of Key Clinical Quality Indicators, and proactively ...

Alps Pharmacy

PRN Nurse Practitioner

Nixa, MO · On-site

Knowledge of computer-based data management programs and information systems, as well as medical ... Demonstrates knowledge of and application of Key Clinical Quality Indicators, and proactively ...

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All JobsClinical Data Management JobsClinical Data Management Jobs in Springfield, MO

Clinical Data Management information

See Springfield, MO salary details

$17

$51

$73

How much do clinical data management jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for clinical data management in Springfield, MO is $51.00, according to ZipRecruiter salary data. Most workers in this role earn between $40.34 and $60.67 per hour, depending on experience, location, and employer.

What is clinical data management?

Clinical data management (CDM) is a critical process in clinical research that involves collecting, cleaning, and managing data generated during clinical trials. The goal is to ensure that the data is accurate, reliable, and compliant with regulatory standards. CDM professionals work closely with researchers, statisticians, and regulatory bodies to validate data and ensure its integrity throughout the study. This process helps in making informed decisions about the safety and efficacy of new drugs or treatments.

What are the key skills and qualifications needed to thrive in clinical data management?

To thrive in Clinical Data Management, you need a strong background in life sciences, attention to detail, and understanding of clinical trial processes, often supported by a relevant degree. Familiarity with industry-standard data management systems such as Medidata Rave or Oracle Clinical, as well as knowledge of CDISC standards and regulatory requirements, is essential. Excellent organizational skills, communication, and problem-solving abilities help ensure data integrity and effective cross-functional collaboration. These skills and qualities are crucial for ensuring high-quality, compliant data that supports clinical research and regulatory submissions.

What are some common challenges faced by professionals in clinical data management, and how can they be addressed?

One of the common challenges in Clinical Data Management is ensuring data accuracy and consistency across multiple sources and formats. This often involves resolving discrepancies and managing large volumes of data within tight timelines. Effective communication with clinical research associates, statisticians, and IT teams is crucial to address data queries promptly and maintain data integrity. Staying updated with regulatory requirements and leveraging advanced data management systems can also help mitigate these challenges and improve overall workflow efficiency.

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

AspectClinical Data ManagementClinical Data Coordinator
ResponsibilitiesDesigning data collection processes, database setup, data validation, and ensuring data quality for clinical trials.Collecting, reviewing, and entering clinical trial data, ensuring accuracy and completeness.
Required SkillsKnowledge of data management systems, clinical trial processes, and data validation techniques.Attention to detail, data entry skills, familiarity with clinical trial documentation.
Work EnvironmentTypically in clinical research organizations, pharmaceutical companies, or CROs.Often within clinical sites or research teams supporting data collection activities.

While both roles focus on clinical trial data, Clinical Data Management involves designing and overseeing data systems and ensuring data integrity, whereas Clinical Data Coordinators handle the day-to-day data collection and entry tasks. Both are essential for successful clinical research but differ in scope and responsibilities.

How do I become a clinical data management?

To become a clinical data manager, typically a bachelor's degree in life sciences, healthcare, or related fields is required. Gaining experience with clinical trial processes, data management tools like EDC systems, and obtaining certifications such as the Society for Clinical Data Management (SCDM) certification can enhance job prospects.

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

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

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

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

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

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

Clinical Data Management jobs near you
Infographic showing various Clinical Data Management job openings in Springfield, MO as of August 2026, with employment types broken down into 50% Full Time, 40% Part Time, and 10% Contract. Highlights an 90% In-person, and 10% Hybrid job distribution, with an average salary of $106,081 per year, or $51 per hour.

Principal Investigator (MD/DO) - Dermatology Clinical Trials

Hawthorne Health

Springfield, MO

$150 - $250/hr

Contractor

Posted 8 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 Role
Hawthorne Health is seeking an experienced Principal investigator (MD/DO) for a part-time, 1099 role. Candidates should have prior experience as a PI or Sub-I on sponsor-initiated clinical trials. This role will lead Dermatology trials within our growing, community-based site network—built to make research efficient, patient-friendly, and investigator-supported.
Responsibilities
  • Accurately document findings and contribute to ongoing clinical trials, registries, or research protocols as applicable.
  • Oversee and manage all aspects of clinical trials conducted at the research site, ensuring adherence to the study protocol, Good Clinical Practice (GCP), ICH guidelines, and all applicable regulatory requirements.
  • Lead and supervise the clinical research team, including sub-investigators, study coordinators, and other site staff.
  • Delegate study-related duties appropriately to qualified personnel and ensure proper training and oversight.
  • Conduct remote review of patient assessments, including physical exams, medical histories, and eligibility screenings, to ensure appropriate participant enrollment.
  • Review and interpret laboratory results, ECGs, and other diagnostic tests.
  • Make critical medical decisions regarding participant care, adverse events, and protocol deviations.
  • Ensure accurate, complete, and timely collection and documentation of all study data.
  • Communicate effectively with sponsors, Contract Research Organizations (CROs), Institutional Review Boards (IRBs), and regulatory authorities.
  • Manage investigational product accountability, storage, and administration according to protocol and with the help of the on-site IP team.
  • Participate in site initiation visits, monitoring visits, audits, and inspections.
  • Maintain continuous medical education and stay current with advancements in clinical research and relevant therapeutic areas.
Requirements
  • Must be an MD with experience leading at least three sponsor initiated trials as a PI or Sub-I.
  • Current, unrestricted medical license.
  • Experience with Dermatology indications in clinical trials and/or in a clinical setting.
  • Demonstrated in-depth knowledge of ICH-GCP guidelines, FDA regulations, and other relevant ethical and regulatory requirements for clinical research.
  • Proven leadership and team management skills.
  • Excellent clinical judgment and decision-making abilities.
  • Strong verbal and written communication skills in English, with the ability to present complex information clearly and concisely.
  • Exceptional organizational skills and meticulous attention to detail.
  • Ability to manage multiple complex studies simultaneously and prioritize tasks effectively.
  • Commitment to ethical conduct and patient safety.
Location
  • This role requires on-site presence approximately twice per month for key visits (or more, depending on study needs), with additional oversight responsibilities performed remotely (approximately 3–5 hours per week).
  • Preference is for Investigator to live within 1.5 hours driving distance of the site. 
This is a 1099 independent contractor opportunity. Compensation may be flexible and adjusted based on experience and qualifications.

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/