Top 1927 Regulatory project manager Jobs in Irving, Tx

Regulatory Data Manager
M/A/R/C Research, LLC —Plano, TX
- $120,000 - $145,000 a year
- Full-time
- Remote
- Computer Science
- 5 years
- System design
- Profit sharing
- Health insurance
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14d
Manager of Institutional Effectiveness & Research
PARKER UNIVERSITY —Dallas, TX
- Doctoral degree
- SQL
- Analysis skills
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Sr. Project Manager
National Life Insurance Company —Addison, TX
- $101,250 - $148,500 a year
- Hybrid work
- Office
- 8 years
- Bachelor's degree
- Benefits from day one
- Life insurance
0000008652.IT MANAGER III.INFO TECH SERVICES
Dallas County —Dallas, TX
- Full-time
- Clean driving record
- Computer Science
- 3 years
Quality & Regulatory Prgrm Mgr
JPS Health Network —Fort Worth, TX
- Full-time
- Research
- Bachelor's degree
- Senior level
Compliance Specialist (Dallas, TX)
TELYRX MANAGEMENT LLC —Irving, TX
- Mid-level
- Organizational skills
- Communication skills
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PI Program Manager, External Outcomes
Methodist Health System —Dallas, TX
- Full-time
- 5 years
- Master's degree
- Senior level
Sr Manager, Project Manager (Hybrid)
RTX Corporate —Richardson, TX
- $132,400 - $251,600 a year
- Full-time
- Hybrid work
- 5 years
- Office
- Experience equivalent to degree accepted
- Paid holidays
- Disability insurance
12d
Regional Housing Manager
Volunteers of America Texas —Euless, TX
- Online Application
- 5 years
- Supervising experience
- Bachelor's degree
- Health insurance
- Paid time off
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Community Manager
Portico Property Management —Irving, TX
- $60,000 - $63,000 a year
- Extended hours
- Background check
- Spanish
- Pass drug screening
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Manager, Healthcare Compliance and Regulatory Affairs
Suvida Healthcare —Dallas, TX
- Full-time
- Remote
- Spanish
- 5 years
- HIPAA
- Paid parental leave
- Paid holidays
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Aviation Project Manager
Vic Thompson Company —Richland Hills, TX
- $110,000 - $175,000 a year
- Full-time
- Hybrid work
- 5 years
- Engineering
- Senior level
- Paid holidays
- Health insurance
Quick Apply
Quality Assurance Policy & Program Coordinator
TimelyCare —Fort Worth, TX
- $65,000 - $70,000 a year
- Full-time
- Remote
- Mid-level
- 2 years
- Paid holidays
- Disability insurance
Quick Apply
Senior Manager, Cyber Audit and Regulatory Engagements
Capital One —Plano, TX
- Email
- Office
- High school diploma or GED
- Analysis skills
- Health insurance
Manager, Quality Assurance
Quest Diagnostics —Lewisville, TX
- Full-time
- Sales
- Writing skills
- Mid-level
Quick Apply
Senior Program Manager
University of North Texas Health at Fort Worth —Fort Worth, TX
- Full-time
- Administrative experience
- University
- Bachelor's degree
2d
Analyst, Regulatory Affairs
Oscar Health —Dallas, TX
- $28.30 - $37.15 an hour
- Overtime
- Remote
- Mid-level
- Microsoft Office
- Bachelor's degree
- Paid parental leave
- Paid holidays
Quick Apply
Operations Excellence Manager (DFW)
J&P Hospitality Management, LLC —Irving, TX
- $80,000 - $90,000 a year
- Weekends as needed
- Spanish
- Microsoft Excel
- Microsoft Outlook
- Travel reimbursement
- Mileage reimbursement
Quick Apply
14d
Manager, Cyber Audit and Regulatory Engagements
Capital One —Plano, TX
- Email
- Office
- High school diploma or GED
- Analysis skills
- Health insurance
Senior Executive of Organizational Strategy & Impact (26-27 SY)
Irving Independent School District —Irving, TX
- $160,477 - $212,729 a year
- Full-time
- School experience
- Spanish
- Office
1d

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regulatory project manager jobs near irving, tx

Regulatory Data Manager

M/A/R/C Research, LLC
Plano, TX

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Job Details

Full-time
$120,000 - $145,000 a year
14 days ago

Benefits

Profit sharing
Health insurance
Dental insurance
Paid time off
Family leave
Vision insurance
401(k) matching

Qualifications

Data visualization software proficiency
Web-based survey tools
Business intelligence report generation
SAS language
SQL
Business intelligence tools
Digital survey tools
Research regulatory compliance
Clinical quality assurance standards
Data visualization projects
Data analytics technologies
Stakeholder management
Database software proficiency

Full 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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Refine Your Search

regulatory project manager jobs in irving, tx

Regulatory Data Manager

Manager of Institutional Effectiveness & Research

Sr. Project Manager

0000008652.IT MANAGER III.INFO TECH SERVICES

Quality & Regulatory Prgrm Mgr

Compliance Specialist (Dallas, TX)

PI Program Manager, External Outcomes

Sr Manager, Project Manager (Hybrid)

Regional Housing Manager

Community Manager

Manager, Healthcare Compliance and Regulatory Affairs

Aviation Project Manager

Quality Assurance Policy & Program Coordinator

Senior Manager, Cyber Audit and Regulatory Engagements

Manager, Quality Assurance

Senior Program Manager

Analyst, Regulatory Affairs

Operations Excellence Manager (DFW)

Manager, Cyber Audit and Regulatory Engagements

Senior Executive of Organizational Strategy & Impact (26-27 SY)

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