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Clinical Data Management Intern Jobs in Michigan

Zimmer Biomet

$14.50 - $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

$14.75 - $19.75/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 - $18.50/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

$15.25 - $20.25/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 - $18.50/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 - $18.75/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 Michigan

Clinical Data Management Intern information

See Michigan salary details

$10

$19

$36

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

As of Aug 17, 2026, the average hourly pay for clinical data management intern in Michigan is $19.61, according to ZipRecruiter salary data. Most workers in this role earn between $15.10 and $21.39 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 Michigan?

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

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

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

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

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

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

Cities in Michigan 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 Michigan as of August 2026, with employment types broken down into 10% Internship, 67% Full Time, 11% Part Time, 6% Temporary, and 6% Contract. Highlights an 88% In-person, 2% Hybrid, and 10% Remote job distribution, with an average salary of $40,799 per year, or $19.6 per hour.

Clinical Data Associate

Shoulder Innovations

Grand Rapids, MI • On-site

$70K - $85K/yr

Full-time

Re-posted 2 days ago

Job description

Shoulder Innovations is a medical device startup that is revolutionizing shoulder replacements. Led by a seasoned team with over a century of orthopedic expertise, we've developed a disruptive shoulder replacement system and secured substantial funding to drive rapid growth. (NYSE: SI).
We're seeking entrepreneurial talent to join us on this exciting journey. Our culture is built on:
  • People First: Authentically human.
  • One Team: Empowered and aligned.
  • Innovation: Bold, creative, and daring.
  • Growth Mindset: Always curious.

Ready to make an impact in orthopedics? Let's grow together!
We are seeking a Clinical Data Associate who is responsible for clinical data management activities across study lifecycle; from start-up through database lock and closeout. This role includes day-to-day data review, query management, and data reconciliation within the Electronic Data Capture (EDC) system, and maintains Power BI dashboards to monitor data cleaning progress, site performance, and study metrics.
Your responsibilities will include, but are not limited to the following:
Data Management
  • Perform comprehensive data management tasks including data review, query generation, and query resolution
  • Support all study phases: Start-up, Execution, Database Lock, and Close-out
  • Perform ongoing data reconciliation across all data streams (e.g., EDC, imaging, third-party vendors)
  • Review discrepancy/edit check output and validation listings per the Data
  • Management Plan (DMP)
  • Resolve answered queries and re-query where appropriate
  • Receive and reconcile imaging data
  • Manage eCRF freeze/lock activities
  • File documentation in the Trial Master File (TMF)
  • Support study closeout and archiving activities, including QC of subject/site CRFs

EDC & Systems
  • Serve as a proficient day-to-day user of the EDC system (e.g., Castor EDC, Rave, or equivalent), including form/field configuration awareness, user access, and data export
  • Generate reports directly from the EDC system to track data cleaning progress and outstanding queries
  • Perform DM quality review and other internal QC checks per applicable EDC systems
  • Support EDC-related testing (edit checks, validation rules, user acceptance testing) during study build and amendments

Reporting & Monitoring (Power BI)
  • Maintains Power BI dashboards and reports to track data cleaning status, query aging, site-level data quality metrics, and monitoring visit findings. Development experience is a plus.
  • Translate data management metrics (e.g., missing data, outstanding queries, protocol deviations) into clear visual reports for internal stakeholders
  • Maintain and troubleshoot existing Power Query/Power BI data pipelines feeding from EDC exports and other source systems
  • Ensure dashboard data accuracy through regular reconciliation against EDC source data

Project & Study Support
  • Attend study-related meetings and teleconferences
  • Track project progress and issue periodic status/metric reports
  • Assist in identifying achievement of milestones per study timelines
  • Participate in finalization and transfer of the clinical database and related documents to the sponsor
  • Participate in internal meetings and internal/external audits as required
  • Maintain awareness of contract scope and study-specific Clinical Data Management Plans

We believe to be successful as a Clinical Data Associate, you will have the following:
  • Bachelor's degree in a health, science, or related discipline, or equivalent experience in clinical research
  • Clinical data associate/management experience at a CRO, pharma, medical device, or biotech company
  • Hands-on experience with EDC systems required (Castor EDC, Rave, Inform, or equivalent)
  • Demonstrated proficiency managing reports/dashboards in Power BI (Power Query/M language experience a plus)
  • Knowledge of current industry standards (e.g., GCP, ICH, CDISC/CDASH)
  • Proficiency with Microsoft Office (Excel, Word); strong Excel skills required
  • Experience working in cross-functional, multi-site clinical trial teams

If you are looking to further your career in a pioneering and evolving industry, apply today for our Clinical Data Associate position. We value and appreciate our employees and will support you with great company culture, opportunities for professional growth, competitive wages, and benefits. To learn more about us, visit us online at https://shoulderinnovations.com.

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