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Remote Clinical Data Management Jobs in Forney, TX

IT America Inc

Data Architect

Dallas, TX · Remote

$65.25 - $84/hr

Remote Duration: Long term contract Job Summary: We are seeking a Data Architect to establish and develop a Data Architecture within the Enterprise Data Management (EDM) team. Reporting to the EDM ...

YO AI Labs

Hospitalist Physician - Remote

Dallas, TX · Remote

$70 - $100/hr

Remote Job Overview We are seeking experienced Hospitalist Physicians to contribute their medical ... Review medical records, including FHIR data and clinical notes , for AI training and quality ...

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All JobsClinical Data Management JobsRemote Clinical Data Management JobsRemote Clinical Data Management Jobs in Forney, TX

Remote Clinical Data Management information

See Forney, TX salary details

$17

$51

$73

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

As of Aug 27, 2026, the average hourly pay for remote clinical data management in Forney, TX is $51.50, according to ZipRecruiter salary data. Most workers in this role earn between $40.72 and $61.30 per hour, depending on experience, location, and employer.

What is remote clinical data management?

Remote clinical data management involves overseeing and maintaining the accuracy, integrity, and security of clinical trial data from a location outside of a traditional office or clinical site. Professionals in this field use digital tools and software to collect, validate, and analyze data gathered during clinical studies, ensuring regulatory compliance and high data quality. This role is essential for supporting drug development and medical research, and typically requires strong attention to detail, knowledge of data management systems, and understanding of clinical trial processes.

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

To thrive as a Remote Clinical Data Manager, you need expertise in clinical data standards, database management, and regulatory compliance, typically supported by a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications such as CDM (Certified Clinical Data Manager) are highly valuable. Strong attention to detail, analytical thinking, and effective communication are crucial soft skills for managing data integrity and collaborating with cross-functional teams remotely. These skills ensure accurate, compliant data collection and reporting, which are vital for successful clinical trials and regulatory submissions.

What are some common challenges faced when managing clinical data remotely, and how can they be addressed?

Remote Clinical Data Management professionals often encounter challenges such as ensuring data integrity, maintaining secure access to sensitive information, and staying aligned with team workflows despite geographic separation. To address these issues, it's important to leverage validated electronic data capture (EDC) systems, follow strict data security protocols, and participate in regular virtual meetings for clear communication. Building strong relationships with cross-functional teams and staying proactive about regulatory updates also contribute to overcoming these remote work challenges.

What job categories do people searching Remote Clinical Data Management jobs in Forney, TX look for?

The top searched job categories for Remote Clinical Data Management jobs in Forney, TX are:

What cities near Forney, TX are hiring for Remote Clinical Data Management jobs?

Cities near Forney, TX with the most Remote Clinical Data Management job openings:

Remote Clinical Data Management jobs near you
Infographic showing various Remote Clinical Data Management job openings in Forney, TX as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 12% Part Time, and 2% Contract. Highlights an 86% Physical, 3% Hybrid, and 11% Remote job distribution, with an average salary of $107,120 per year, or $51.5 per hour.

Regulatory Data Manager

M/A/R/C Research, LLC

Plano, TX • Remote

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 23 days ago

Job description

Regulatory Data Manager

Location: Remote (U.S.)
Department: Compliance & Data Management
Reports To: SVP, Compliance & Data Management

About Us

We are a leading marketing and regulatory research organization specializing in complex, high-quality studies that support business decision-making, public health initiatives, and regulated research programs. Our work combines advanced data collection technologies, rigorous quality standards, and defensible analytics to deliver reliable insights for clients across commercial, healthcare, and regulated sectors.

We are seeking an experienced Regulatory Data Manager (RDM) to lead the planning, implementation, quality control, and governance of regulated research data. This role ensures data integrity, regulatory compliance, audit readiness, and timely delivery of high-quality datasets and supporting documentation throughout the research lifecycle.

#LI-Remote

Position Summary

The Regulatory Data Manager is responsible for designing, managing, validating, reconciling, and reporting regulated research data from protocol development through database lock and final reporting suitable for client submission to the FDA. The role serves as the primary steward of study data, ensuring that data collection systems, documentation, quality controls, and deliverables meet regulatory, client, and internal quality requirements. This position collaborates closely with project management, field operations, biostatistics, analytics, compliance, and external stakeholders to support accurate, compliant, and submission-ready research execution.

Key ResponsibilitiesData Management

         Lead all data management activities across multiple regulated research studies.

         Develop and maintain SOPs, and manage drafting of:

o   Data Management Plans (DMPs)

o   Data Validation Plans

o   CRF/eCRF specifications

o   Data Review Plans

o   Database Lock Plans

o   Data Transfer Specifications

o   Any other client required plans and specifications

         Design, review, and validate electronic data capture (EDC) systems and online survey platforms.

         Ensure accurate mapping of protocol requirements into study databases and collection instruments.

         Manage study metadata, coding standards, edit checks, and validation rules.

         Oversee database development, user acceptance testing (UAT), and production deployment, including CRF design, EDC configuration support, validation checks, and comprehensive data documentation.

         Work with clients' electronic trial master file systems to ensure all data management documentation is correctly formatted, uploaded and quality assured.

Data Quality and Compliance

         Establish and monitor data quality metrics across studies.

         Conduct routine data review, cleaning, query generation, and discrepancy resolution.

         Support risk-based quality management processes and inspection readiness programs.

         Ensure compliance with:

o   FDA regulations

o   21 CFR Part 11

o   CDISC standards

o   HIPAA

o   ICH-GCP

o   GDPR (where applicable)

o   Internal SOPs and quality requirements, including documentation of data accuracy, integrity, security, audit trails, and regulatory compliance throughout the study lifecycle.

         Perform reconciliation of external vendor data including laboratory and other test data, qualitative coding, digital health, and other ancillary datasets, if required.

Database Lock and Reporting

         Coordinate interim and final database lock and unlock activities.

         Ensure all outstanding queries and reconciliation activities are resolved before lock.

         Produce data listings, metrics, status reports, and quality dashboards.

         Deliver clean, analyzable datasets to biostatistics and analytics teams.

         Support preparation of study reports, technical reports, regulatory submission materials, and audit responses.

Stakeholder Collaboration

         Serve as lead data management representative on assigned studies.

         Collaborate with:

o   Clients and Sponsors

o   Project Managers

o   Research Directors

o   Statisticians

o   Data Scientists

o   Compliance Teams

         Participate in study design discussions and protocol reviews to ensure data collection feasibility and quality.

         Provide guidance and training on data management processes, system usage, and study documentation expectations while serving as the primary data management contact for assigned studies.

Process Improvement and Innovation

         Contribute to SOP development and continuous improvement initiatives.

         Evaluate new technologies, automation tools, and AI-enabled data management solutions.

         Support development of standards for decentralized studies, digital data collection, and real-world data integration.

         Promote best practices aligned with SCDM Good Clinical Data Management Practices (GCDMP), and CDISC/TIG.

Requirements

Required Qualifications

         Bachelor's or advanced degree in Life Sciences, Health Informatics, Biostatistics, Epidemiology, Public Health, Computer Science, or a related field.

         Minimum 5 years of regulatory data management experience.

         Experience supporting regulated research in nicotine science (preferred), healthcare research, pharmaceutical, biotechnology, medical device, CRO, or FDA-related studies.

         Strong understanding of regulated study processes, data management principles, data quality controls, GCP requirements, data validation, and applicable regulatory frameworks.

         Experience using EDC/eTMF platforms such as Decipher, Medidata Rave, REDCap, Oracle Clinical, Veeva, TrialKit, MEDRIO or similar systems.

         Working knowledge of SQL, SAS, Power BI, and data visualization/reporting tools.

Preferred Qualifications

         Experience supporting FDA submissions or pivotal studies, preferably in the nicotine science space.

         Knowledge of CDISC standards including CDASH, SDTM, and ADaM.

         Experience with electronic patient-reported outcomes (ePRO/eCOA).

         Familiarity with real-world evidence (RWE) data sources, electronic health records such as Epic, decentralized clinical trials, and digital endpoints.

         CCDM (Certified Clinical Data Manager) or other relevant regulatory certification.

         Experience managing external vendors and data integrations.

         Knowledge of AI-enabled data review and quality management technologies.

Success Factors

The ideal candidate:

         Demonstrates meticulous attention to detail.

         Maintains a strong commitment to data integrity.

         Thrives in a highly regulated environment.

         Communicates effectively with both technical and non-technical stakeholders.

         Balances quality, compliance, and operational efficiency.

         Takes ownership of data from study startup through closeout.

Why Join Us

         Work on high-impact research supporting public health and regulatory decision-making.

         Collaborate with cross-functional experts in research, analytics, and compliance.

         Opportunity to help shape next-generation data governance and AI-enabled research operations.

         Opportunity for professional growth

Benefits

  • M/A/R/C is committed to providing an exceptional work environment and excellent benefits.
  • Health Care Plan (Medical, Dental, Vision & Supplemental)
  • Retirement Plan (401k with Company Match)
  • Profit Sharing
  • Paid Time Off (Vacation, Sick & Public Holidays)
  • Family Leave (Maternity, Paternity)
  • Training & Development

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