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Contract Clinical Data Manager Jobs in Michigan (NOW HIRING)

SER Metro-Detroit

Data Performance Manager

Detroit, MI · On-site

Data Performance Manager DIVISION: Adult & Youth Services DEPARTMENT: Data Management LOCATION ... Detroit contracts/services. Analyzes performance outcomes by comparing actual to planned goals ...

SER Metro-Detroit

Data Performance Manager

Detroit, MI · On-site

Data Performance Manager DIVISION: Adult & Youth Services DEPARTMENT: Data Management LOCATION ... Detroit contracts/services. Analyzes performance outcomes by comparing actual to planned goals ...

Alcanza

Data Entry Coordinator

Farmington, MI · On-site

Managing data entry into computer systems for clinical trials, including entering patient data into eDC and other software * Reviewing patient charts and other medical records to ensure data is ...

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Contract Clinical Data Manager information

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$17

$49

$71

How much do contract clinical data manager jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for contract clinical data manager in Michigan is $49.83, according to ZipRecruiter salary data. Most workers in this role earn between $39.38 and $59.28 per hour, depending on experience, location, and employer.

What does a contract clinical data manager do?

A Contract Clinical Data Manager typically spends their days overseeing data collection, validation, and entry processes, ensuring that clinical trial data meets quality and regulatory standards. This role often involves close collaboration with data entry teams, biostatisticians, and clinical project managers to resolve discrepancies and maintain data integrity. Daily responsibilities may include designing case report forms, conducting data reviews, managing database queries, and preparing data for interim or final analyses. Working on a contract basis, you may manage multiple projects concurrently and must be adaptable to varying timelines and sponsor requirements.

What is a contract clinical data manager?

A Contract Clinical Data Manager is a temporary or freelance professional responsible for overseeing and managing clinical trial data for pharmaceutical, biotech, or CRO companies. They ensure data integrity, compliance with regulatory standards, and support database design, data cleaning, and reporting. Contract roles offer flexibility and typically involve working on specific projects or trials for a set duration.

What are the key skills and qualifications needed to thrive as a contract clinical data manager?

To thrive as a Contract Clinical Data Manager, you need strong expertise in clinical data management, a background in life sciences, and familiarity with regulatory guidelines such as FDA or ICH-GCP. Proficiency in database systems like Medidata Rave or Oracle Clinical, coupled with knowledge of CDISC standards and, in many cases, a CCDM certification, is highly valued. Excellent attention to detail, strong organizational skills, and effective communication help distinguish top performers in this role. These abilities are crucial for ensuring compliant, high-quality data that supports successful clinical trials on a contractual or project basis.

What are the most commonly searched types of Clinical Data Manager jobs in Michigan? The most popular types of Clinical Data Manager jobs in Michigan are:
What are popular job titles related to Contract Clinical Data Manager jobs in Michigan? For Contract Clinical Data Manager jobs in Michigan, the most frequently searched job titles are:
What job categories do people searching Contract Clinical Data Manager jobs in Michigan look for? The top searched job categories for Contract Clinical Data Manager jobs in Michigan are:
What cities in Michigan are hiring for Contract Clinical Data Manager jobs? Cities in Michigan with the most Contract Clinical Data Manager job openings:
Contract Clinical Data Manager jobs near you
Infographic showing various Contract Clinical Data Manager job openings in Michigan as of August 2026, with employment types broken down into 71% Full Time, 7% Part Time, and 22% Contract. Highlights an 87% In-person, and 13% Remote job distribution, with an average salary of $103,640 per year, or $49.8 per hour.

Clinical Data Associate

Shoulder Innovations

Grand Rapids, MI • On-site

$70K - $85K/yr

Full-time

Posted 25 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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