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Part Time Clinical Data Manager Jobs (NOW HIRING)

Specialised Part-Time Consulting OpportunityWe are sharing a specialised part-time consulting opportunity for experienced clinical data management professionals with deep expertise in CDISC standards ...

Specialised Part-Time Consulting OpportunityWe are sharing a specialised part-time consulting opportunity for experienced clinical data management professionals with deep expertise in CDISC standards ...

$32/hr

At Carta Healthcare, we are revolutionizing the way healthcare data is managed and used with innovative software solutions. Position Overview: As a Part-Time Clinical Data Abstractor , you will be ...

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Part Time Clinical Data Manager information

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How much do part time clinical data manager jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for part time clinical data manager 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 does a part time clinical data manager do?

A Part Time Clinical Data Manager is responsible for collecting, managing, and ensuring the accuracy of data generated from clinical trials, but on a reduced or flexible schedule. Their duties include designing data collection systems, monitoring data quality, ensuring compliance with regulatory standards, and collaborating with clinical research teams. Working part-time allows them to handle these responsibilities while maintaining a balanced workload, often supporting multiple studies or phases as needed. They play a crucial role in ensuring that clinical trial data is reliable and ready for statistical analysis and regulatory submission.

How do part time clinical data managers typically balance project deadlines and workload with a reduced schedule?

Part-time Clinical Data Managers often work closely with project leads to prioritize tasks and ensure that critical deadlines are met despite fewer working hours. Effective time management, clear communication, and leveraging project management tools are key strategies in this role. Collaboration with full-time team members is essential to maintain data quality and project continuity. Employers generally provide flexible work arrangements and may assign specific portions of projects that align with the part-time schedule, enabling a manageable workload while still contributing significantly to clinical research outcomes.

What are the key skills and qualifications needed to thrive as a part time clinical data manager, and why are they important?

To thrive as a Part Time Clinical Data Manager, you need a background in life sciences or a related field, experience with clinical data management, and attention to detail. Familiarity with data management systems like Medidata Rave, Oracle Clinical, and knowledge of regulatory standards such as GCP and CDISC are typically required. Strong organizational skills, problem-solving, and effective communication are valuable soft skills in this position. These competencies ensure accurate data collection, regulatory compliance, and successful collaboration within clinical research teams.

What is the difference between Part Time Clinical Data Manager vs Part Time Clinical Research Coordinator?

AspectPart Time Clinical Data ManagerPart Time Clinical Research Coordinator
CredentialsTypically requires a degree in health sciences, life sciences, or related field; certifications like CDMP are commonRequires a degree in health sciences or related field; certifications are less common but may include CRC certification
Work EnvironmentWorks primarily with data management systems, databases, and electronic records in clinical trial settingsManages study logistics, patient interactions, and site coordination in clinical trial sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsResearch institutions, hospitals, clinical trial sites

While both roles support clinical trials, the Part Time Clinical Data Manager focuses on data accuracy and database management, whereas the Part Time Clinical Research Coordinator handles study logistics and patient interactions. Understanding these differences helps in choosing the right career path or job search focus.

How do I become a part time clinical data manager?

To become a part-time clinical data manager, candidates typically need a bachelor's degree in health sciences, life sciences, or a related field, along with experience in clinical research or data management. Proficiency in data management tools like EDC systems and knowledge of regulatory standards such as GCP are also important. Gaining relevant certifications, such as CDMP, can enhance job prospects in this flexible role.
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Infographic showing various Part Time Clinical Data Manager job openings in the United States as of August 2026, with employment types broken down into 87% Full Time, 12% Part Time, and 1% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $118,909 per year, or $57.2 per hour.

Clinical Data Manager

24-MAG LLC

Manhattan, NY โ€ข Remote

Part-time, Contractor

This job post hasย expired 1 day ago.ย Applications are no longer accepted.


Job description

Specialised Part-Time Consulting OpportunityWe are sharing a specialised part-time consulting opportunity for experienced clinical data management professionals with deep expertise in CDISC standards, SDTM conformance, EDC build, database lock, and end-to-end clinical data room oversight.

This role supports advanced clinical research workflows involving synthetic clinical data generation, data-room quality control, and cross-document reconciliation. Selected professionals will help ensure that protocols, datasets, tables, listings, figures, narratives, and downstream metrics remain internally consistent, realistic, and fully traceable.

Key ResponsibilitiesClinical Data GenerationLead the generation and validation of high-quality synthetic clinical trial dataEnsure data structures reflect realistic clinical development and data-management workflowsReview patient-level records for completeness, consistency, and plausibilityMaintain alignment between protocol requirements and generated datasetsIdentify inconsistencies or missing relationships across clinical data artifactsClinical Data Room OversightReview complete clinical data rooms for realism, internal consistency, and traceabilityEnsure information reconciles across protocols, raw datasets, derived datasets, TLFs, and narrativesVerify that patient-level data flows correctly across all downstream outputsIdentify discrepancies between source information and summary metricsApply end-to-end data-management judgement rather than reviewing files in isolationCDISC & SDTM ConformanceApply hands-on knowledge of CDISC and SDTM standardsReview dataset structures, variables, domains, controlled terminology, and conformanceIdentify mapping, formatting, and traceability issuesEvaluate whether transformed datasets accurately reflect underlying source dataSupport consistent application of standards across study-level data packagesEDC Build & Database LifecycleApply experience across EDC design, build, validation, and study conductReview CRF structures, edit checks, data-entry logic, and downstream data flowEvaluate data-cleaning and reconciliation workflowsAssess readiness for database freeze and lockIdentify unresolved issues that could compromise final data integrityCross-File ReconciliationVerify consistency between patient records, datasets, TLFs, narratives, and summary outputsEnsure participants referenced in one artifact are represented correctly across related filesIdentify mismatched values, missing records, inconsistent denominators, or contradictory outputsAssess whether folded or aggregate metrics reconcile to patient-level dataMaintain traceability from source data through final reporting outputsData Room Quality ControlValidate synthetic data rooms for completeness, realism, and professional qualityIdentify implausible clinical-data patterns or inconsistenciesReview whether expected artifacts are present and appropriately linkedEvaluate data lineage and evidence provenance across the data packageApply a verify-before-finalise approach to all major outputsTask & Reference Output DevelopmentDesign realistic clinical data-management tasks based on authentic workflowsDevelop clear prompts, expected outputs, and evaluation criteriaProduce authoritative reference solutions for data-room and reconciliation tasksDefine standards for correctness, traceability, and completenessCreate tasks that reflect how experienced clinical data managers work in practiceIdeal Profile5+ years of professional clinical data management experience, with 10โ€“25 years preferredDemonstrated managerial oversight of complete clinical data roomsStrong hands-on expertise with CDISC and SDTM conformanceExperience managing EDC workflows from build through database lockStrong understanding of clinical datasets, TLFs, narratives, and cross-file reconciliationAbility to identify inconsistencies across patient-level and aggregate dataExperience ensuring traceability across protocols, datasets, outputs, and reporting artifactsStrong knowledge of clinical data lifecycle, cleaning, validation, and database closeoutComfortable leading complex data-quality and reconciliation workflowsNo specific degree is required; substantial hands-on experience is the primary qualificationStrong written communication and ability to document data-quality findings clearlyBased in the United States, Canada, or FranceEngagement DetailsPart-time independent contractor engagementFully remoteMinimum availability of approximately 20โ€“25 hours per weekAvailability of 30+ hours per week is strongly preferredFlexible scheduling based on project requirementsCompensation: $90โ€“$140/hourWork may include clinical data generation, data-room QC, CDISC/SDTM validation, reconciliation, and task developmentProjects may be extended, shortened, or concluded based on project needs and performanceWork must be completed without using confidential or proprietary information belonging to any employer, sponsor, client, institution, or other third partyH1-B and STEM OPT support is unavailable for this engagementAbout the PlatformThis opportunity is available through 24-MAG LLC. We connect experienced professionals with remote consulting opportunities across technical, evaluation, and project-based workstreams.

By submitting this application, you acknowledge that your information may be processed by 24-MAG LLC for recruitment and opportunity matching in accordance with our Privacy Policy: https://www.24-mag.com/privacy-policy.