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Ecrf Clinical Data Jobs (NOW HIRING)

ProPharma Group

Clinical Data Manager

Charleston, WV · On-site +1

Clinical Data Manager The Clinical Data Manager performs activities pertaining to the conduct of ... eCRF Completion Guidelines. * Participate in User Acceptance Testing (UAT), as needed.

ProPharma Group

## Clinical Data ManagerApplylocations: United Statestime type: Full timeposted on: Posted Todayjob ... and eCRF Completion Guidelines.* Participate in User Acceptance Testing (UAT), as needed.

Clinovo

Sr Clinical Data Manager

Waltham, MA · On-site

Develop and oversee eCRFs, eCRF completion guidelines, Data Management Plans (DMPs), data review ... Monitor clinical data flow and ensure timely, accurate, and high-quality data availability for ...

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Ecrf Clinical Data information

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How much do ecrf clinical data jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for ecrf clinical data in the United States is $57.17, according to ZipRecruiter salary data. Most workers in this role earn between $45.19 and $68.03 per hour, depending on experience, location, and employer.

What is an eCRF Clinical Data professional?

An ECRF Clinical Data professional is responsible for managing and overseeing electronic case report forms (eCRFs) used in clinical trials to collect, clean, and validate patient data. They ensure that the data entered into eCRFs is accurate, complete, and compliant with regulatory standards. Their role is crucial in supporting the integrity of clinical research by maintaining high-quality data throughout the study lifecycle. ECRF Clinical Data professionals also collaborate with study teams, monitor data discrepancies, and facilitate timely data entry and query resolution.

What are the key skills and qualifications needed to thrive as an eCRF Clinical Data professional?

To thrive as an eCRF Clinical Data Specialist, you need a solid understanding of clinical research processes, data management principles, and experience with electronic Case Report Forms (eCRF), often supported by a degree in life sciences or a related field. Familiarity with data capture systems like Medidata Rave, Oracle Clinical, and knowledge of regulatory standards such as GCP and CDISC is typically required. Attention to detail, strong analytical thinking, and effective communication are crucial soft skills for ensuring data integrity and collaborating with cross-functional teams. These skills are essential to ensure accurate, compliant clinical data collection that supports reliable research outcomes.

How does an eCRF Clinical Data professional typically collaborate with study teams during a clinical trial?

An eCRF Clinical Data professional works closely with clinical research associates, data managers, and biostatisticians to ensure data integrity throughout a clinical trial. They are responsible for designing and maintaining electronic case report forms (eCRFs), resolving data queries, and ensuring that collected data meets regulatory standards. Effective communication and teamwork are essential, as eCRF data professionals often participate in study meetings, provide training to site staff, and coordinate with IT teams to troubleshoot technical issues. This collaborative environment helps ensure accurate and timely data collection, which is critical to the success of the trial.

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

AspectEcrf Clinical DataClinical Data Coordinator
Primary RoleDesigning, managing, and ensuring the accuracy of electronic case report forms (eCRFs) for clinical trialsCollecting, reviewing, and managing clinical trial data to ensure quality and compliance
Required SkillsKnowledge of EDC systems, clinical trial processes, data managementData entry, quality control, understanding of clinical protocols
Work EnvironmentPharmaceutical companies, CROs, clinical research settingsClinical sites, research organizations, CROs

While both roles involve clinical data, Ecrf Clinical Data specialists focus on designing and managing electronic case report forms, whereas Clinical Data Coordinators handle data collection and quality control at clinical sites. Both roles are essential in clinical trials but differ in scope and responsibilities.

Clinical Data Associate

Grand Rapids, MI • On-site

Shoulder Innovations
Medical Equipment and Supplies Manufacturing • 1 - 10 employees
Learn more about Shoulder Innovationsexternal

Other

Re-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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