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Clinical Data Management Intern Jobs in Missouri

Zimmer Biomet

$14.25 - $19/hr

What You Can Expect The Clinical Applications Intern is responsible for providing support to the Biostatistics & Clinical Data Management (BCDM) department in the development and maintenance of ...

Zimmer Biomet

$13.75 - $18.25/hr

What You Can Expect The Clinical Applications Intern is responsible for providing support to the Biostatistics & Clinical Data Management (BCDM) department in the development and maintenance of ...

Zimmer Biomet

$13.75 - $18.25/hr

What You Can Expect The Clinical Applications Intern is responsible for providing support to the Biostatistics & Clinical Data Management (BCDM) department in the development and maintenance of ...

Zimmer Biomet

$14.75 - $19.50/hr

What You Can Expect The Clinical Applications Intern is responsible for providing support to the Biostatistics & Clinical Data Management (BCDM) department in the development and maintenance of ...

Zimmer Biomet

$14.25 - $19/hr

What You Can Expect The Clinical Applications Intern is responsible for providing support to the Biostatistics & Clinical Data Management (BCDM) department in the development and maintenance of ...

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All JobsClinical Data Management Intern JobsClinical Data Management Intern Jobs in Missouri

Clinical Data Management Intern information

See Missouri salary details

$11

$21

$39

How much do clinical data management intern jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for clinical data management intern in Missouri is $21.11, according to ZipRecruiter salary data. Most workers in this role earn between $16.25 and $22.98 per hour, depending on experience, location, and employer.

What does a clinical data management intern do?

A Clinical Data Management Intern assists in the collection, organization, and validation of clinical trial data to ensure its accuracy and integrity. They support senior data managers by performing data entry, cleaning datasets, conducting quality checks, and generating reports. Interns often learn about regulatory requirements, data management systems, and Good Clinical Practice (GCP) guidelines. Their work is crucial for ensuring that clinical trial results are reliable and meet industry standards.

What kinds of projects or tasks can a clinical data management intern expect to work on during their internship?

As a Clinical Data Management Intern, you can anticipate supporting tasks such as reviewing clinical trial data for accuracy, assisting with database setup and validation, and ensuring data is entered and managed according to protocols. You'll often collaborate closely with data managers, statisticians, and clinical research teams to help maintain data integrity and compliance with regulatory standards. This hands-on experience provides valuable exposure to industry tools and processes, which is a strong foundation for advancing into more specialized roles within clinical research.

What are the key skills and qualifications needed to thrive as a clinical data management intern, and why are they important?

To excel as a Clinical Data Management Intern, you need a solid understanding of clinical research concepts, attention to detail, and at least a bachelor's degree in life sciences or related fields. Familiarity with data management tools like Oracle Clinical, Medidata Rave, and basic knowledge of regulatory standards such as GCP are highly valuable. Strong organizational skills, analytical thinking, and effective communication help you collaborate with cross-functional teams and maintain data integrity. These skills are crucial for ensuring accurate, compliant, and reliable clinical data that supports successful research outcomes.

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

AspectClinical Data Management InternClinical Data Coordinator
Required CredentialsTypically pursuing or recent graduate in life sciences or related fieldBachelor's degree in life sciences, health informatics, or related field
Work EnvironmentInternship setting, often in pharmaceutical or biotech companiesFull-time role in clinical research teams, often in hospitals or research organizations
Employer & Industry UsageUsed in pharmaceutical, biotech, and clinical research companies for entry-level rolesCommon in clinical research organizations, hospitals, and pharmaceutical companies

The Clinical Data Management Intern typically is a temporary, entry-level position aimed at gaining experience in clinical data processes, while the Clinical Data Coordinator is a full-time role responsible for managing and ensuring the quality of clinical data during trials. Both roles require knowledge of data management principles, but the intern position is more educational, whereas the coordinator role involves more responsibility and hands-on data oversight.

What are the most commonly searched types of Clinical Data Management jobs in Missouri?

The most popular types of Clinical Data Management jobs in Missouri are:

What are popular job titles related to Clinical Data Management Intern jobs in Missouri?

For Clinical Data Management Intern jobs in Missouri, the most frequently searched job titles are:

What job categories do people searching Clinical Data Management Intern jobs in Missouri look for?

The top searched job categories for Clinical Data Management Intern jobs in Missouri are:

What cities in Missouri are hiring for Clinical Data Management Intern jobs?

Cities in Missouri with the most Clinical Data Management Intern job openings:

Clinical Data Management Intern jobs near you
Infographic showing various Clinical Data Management Intern job openings in Missouri as of August 2026, with employment types broken down into 3% Internship, 75% Full Time, 9% Part Time, 3% Temporary, and 10% Contract. Highlights an 77% In-person, 6% Hybrid, and 17% Remote job distribution, with an average salary of $43,907 per year, or $21.1 per hour.

Clinical Data Manager - Data Integrity & Investigation

Rdi Web

California, MO • On-site

$80 - $110/hr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 15 days ago

Job description

Clinical Data Manager — Data Integrity & Investigation

Own the data. Find the true story it's hiding.

About RDI

RDI is a CRO purpose-built for diagnostics. Since 2008 we've run 300+ IVD trials for the largest test makers in the world. Our job is to get better tests to market faster — with cleaner data, smarter tools, and zero nonsense.

The Role

When a new assay disagrees with the predicate, somebody has to figure out why. Is it the test? The specimen? The site? A single keystroke at data entry? Most "data people" report the discordance and move on. We're looking for the one who treats it as a case to crack.

You’ll own subject- and sample-level data across 20–30 concurrent method‑comparison and specimen‑collection studies — and your real job is to make sure the dataset tells the truth. Not the convenient version. Not the version that makes a result look cleaner than it is. What actually happened. You check every cell because the truth lives in the cells, and you chase every anomaly to root cause because "looks off" is where the work starts.

What this role actually is
  • Investigation— you trace discordant results, outliers, and drift to their source and determine whether you're looking at real signal or a data artifact.
  • Source‑level verification— every critical field traced to origin; you’re the one who finds the single transcription error in 10,000 rows.
  • Reconciliation— lab results, sample inventory, demographics, and visit dates agree across systems, or you find out why.
  • Telling it straight— you can stand in front of the science and regulatory team and explain what the data means, honestly — and hold the line when someone wants a prettier story than the data supports.
  • Database lock— you’re accountable for the dataset that goes to FDA, and you’ll defend every value in it under audit.
  • ALCOA+ / 21 CFR Part 11— integrity isn’t a checkbox here, it’s the whole job.
How you’ll work
  • Dig directly into raw data wherever it lives — EDC, exports, source documents — to get to the bottom of what it’s saying.
  • Build and refine eCRFs and edit checks that catch bad data at entry (Castor today; we’re building our own EDC — you’ll help shape the system that makes the truth easy to see).
  • Set the standard for “clean” with our Philippines‑based data team.
  • Sit between clinical, lab, regulatory, and engineering — your dataset is the thing all of them trust.
  • 3+ years clinical data management in a regulated environment (IVD/diagnostics a strong plus).
  • An investigative instinct— you chase anomalies to root cause and aren’t satisfied until you know why, not just what.
  • Hands‑on EDC experience (Castor, Cloudbyz, REDCap, Medidata, or similar) and comfort working directly with raw data — we care that you get to the bottom of it, not which tool you reach for.
  • Command of the integrity discipline: SDV, query management, reconciliation, database lock, ALCOA+, Part 11.
  • Enough biostatistical literacy to tell real signal from artifact (concordance, outliers, method comparison) — without torturing the data to fit a conclusion.
  • The spine to tell the true story even when it’s not the one people want to hear.
  • Bonus: FDA submission exposure (510(k), CLIA waiver); GCP/ICH familiarity.
What we’re not looking for
  • Someone who reports the number without asking whether it’s real.
  • A "storyteller" who starts with the conclusion and back‑fills the data to match.
  • Extract, export, move on.
  • Medical/Dental/Vision
  • 401k/IRA
  • Life (Basic, Voluntary & AD&D)
  • Unlimited PTO (Vacation, Sick)
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