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Clinical Research Data Manager Jobs in Reston, VA

Guidehouse

Research Nurse Specialist

Bethesda, MD · On-site

$74K - $124K/yr

Manage clinical research data and support data quality assurance. What You Will Need: * Bachelor's degree in nursing or related field with at least 2 years of nursing experience. * Active, current ...

Guidehouse

Research Nurse Specialist

Bethesda, MD · On-site

$98K - $163K/yr

Manage clinical research data and support data quality assurance. What You Will Need: * Bachelor's degree in nursing or related field with at least 4 years of nursing experience. * Active, current ...

Guidehouse

Research Nurse Specialist

Bethesda, MD · On-site

$98K - $163K/yr

Manage clinical research data and support data quality assurance. What You Will Need: * Bachelor's degree in nursing or related field with at least 4 years of nursing experience. * Active, current ...

Guidehouse

Research Nurse Specialist

Bethesda, MD · On-site

$74K - $124K/yr

Manage clinical research data and support data quality assurance. What You Will Need: * Bachelor's degree in nursing or related field with minimum 2+ years of nursing experience. * Active, current ...

Axle

Clinical Research Coordinator

Bethesda, MD

$26 - $34.50/hr

We work with some of the top research organizations and facilities in the country including ... Coordinate activities among investigators, regulatory staff, data managers, and clinical teams

Axle

Clinical Research Coordinator

Bethesda, MD · On-site

$26 - $34.50/hr

We work with some of the top research organizations and facilities in the country including ... Coordinate activities among investigators, regulatory staff, data managers, and clinical teams

ClearanceJobs

Research Nurse Specialist Jobs

Bethesda, MD · On-site

$74K - $124K/yr

Manage clinical research data and support data quality assurance. What You Will Need: * Bachelor's degree in nursing or related field with minimum 2+ years of nursing experience. * Active, current ...

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Clinical Research Data Manager information

See Reston, VA salary details

$51K

$111.7K

$196.6K

How much do clinical research data manager jobs pay per year?

As of Aug 18, 2026, the average yearly pay for clinical research data manager in Reston, VA is $111,668.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,300.00 and $127,400.00 per year, depending on experience, location, and employer.

What is a clinical research data manager?

A Clinical Research Data Manager is a professional responsible for collecting, organizing, and managing the data generated during clinical trials and research studies. They ensure that the data is accurate, complete, and complies with regulatory standards. Their work is crucial for the integrity of clinical research, as it allows researchers to draw valid conclusions from the study. Data managers work closely with clinical teams, statisticians, and regulatory bodies to maintain high-quality data throughout the research process.

What are some common challenges faced by clinical research data managers during multi-site trials?

Clinical Research Data Managers often encounter challenges coordinating data collection across multiple research sites, such as ensuring consistent data entry, handling discrepancies, and maintaining data quality standards. Effective communication with site staff and timely resolution of data queries are essential to minimize delays and errors. Utilizing robust electronic data capture (EDC) systems and standardized procedures helps, but proactive problem-solving and attention to detail remain crucial for success in this role.

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

To thrive as a Clinical Research Data Manager, you need a solid background in life sciences, data management principles, and experience with clinical trial processes, often backed by a relevant bachelor's degree. Proficiency in electronic data capture (EDC) systems, database management tools like SQL, and familiarity with regulatory standards such as GCP are essential. Strong attention to detail, problem-solving abilities, and effective communication skills help ensure data integrity and smooth collaboration across research teams. These skills are crucial for maintaining high-quality, compliant data that support successful clinical trials and regulatory submissions.

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

AspectClinical Research Data ManagerClinical Research Coordinator
Primary RoleOversees data collection, management, and quality control of clinical trial data.Coordinates daily trial activities, patient recruitment, and site management.
Required SkillsData management, database systems, regulatory compliance.Patient interaction, study protocol adherence, site coordination.
Work EnvironmentData centers, clinical trial sites, research organizations.Clinical sites, hospitals, research facilities.
Common CertificationsCDMP, SAS, or related data management certifications.GCP certification, clinical trial training.

While both roles support clinical research, the Clinical Research Data Manager focuses on data integrity and management, whereas the Clinical Research Coordinator handles trial operations and participant coordination. Understanding these differences helps in choosing the right career path or job search focus.

What are popular job titles related to Clinical Research Data Manager jobs in Reston, VA?

For Clinical Research Data Manager jobs in Reston, VA, the most frequently searched job titles are:

What job categories do people searching Clinical Research Data Manager jobs in Reston, VA look for?

The top searched job categories for Clinical Research Data Manager jobs in Reston, VA are:

What cities near Reston, VA are hiring for Clinical Research Data Manager jobs?

Cities near Reston, VA with the most Clinical Research Data Manager job openings:

Clinical Research Data Manager jobs near you
Infographic showing various Clinical Research Data Manager job openings in Reston, VA as of August 2026, with employment types broken down into 87% Full Time, 11% Part Time, and 2% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $111,668 per year, or $53.7 per hour.

Scientific Project Manager (Biomedical Data Coordination)

Digital Infuzion

Rockville, MD • On-site, Remote

$90K - $110K/yr

Full-time

Re-posted 2 days ago

Job description

We believe that by equipping researchers with rapid insights and providers with tailored, on-demand data, we can help people lead better, healthier lives. At Digital Infuzion, we harness innovative healthcare solutions and cutting-edge bioinformatics to make meaningful impacts in patient care.
Our team thrives in a creative, open, and growth-oriented environment, guided by our core values:
Outcomes First: Focusing on what matters most and making timely, informed decisions.
Innovative: Embracing creativity and continuous improvement to drive novel solutions.
Radical Candor: Communicating openly and honestly, balancing direct feedback with genuine care.
Never Satisfied: Pursuing excellence and continuous growth beyond the status quo.
Resilient: Adapting and persevering through challenges, turning obstacles into opportunities.
If you're passionate about leveraging technology to improve healthcare and want to work in an environment that values innovation and collaboration, we may have just the opportunity for you.
Position Overview
Digital Infuzion delivers Data Coordination Services to large multi-center research networks through a comprehensive scientific data management, sharing, and analysis platform. We are looking for an exceptional individual to serve as the Scientific Project Manager for a Data Coordination Services program supporting the National Institute of Allergy and Infectious Diseases.
In this role, you will provide scientific and operational coordination for a multidisciplinary team supporting a mission-driven NIH program focused on infectious disease, vaccine development, translational research, and related scientific initiatives. The role will bring together expertise in biomedical research, data management, informatics, data quality, and scientific communications. Serving as a key liaison among program leadership, government stakeholders, investigators, data managers, and technical teams, the Coordinator will help ensure that scientific priorities and stakeholder needs are clearly understood and addressed. This individual will translate those priorities into coordinated activities, effective data management strategies, well-defined technical requirements, and high-quality program deliverables.
Who you are
  • The ideal candidate is a scientifically trained professional with experience coordinating complex biomedical, public health, clinical, translational, or research-focused programs.
  • You are a natural organizer, task manager, and action-oriented problem solver.
  • You have a desire to apply your scientific or research background to support programs that enable biomedical discovery and public health impact.
  • You are comfortable working with scientists, data analysts, informatics professionals, communications specialists, technical teams, and government stakeholders.
  • You are skilled at facilitating discussions, identifying areas of agreement, resolving ambiguity, and translating stakeholder needs into clear requirements and next steps.
  • You have a strong sense of quality and can help teams maintain clear processes, documentation, timelines, and expectations.
  • You are interested in scientific data sharing, research coordination, and the role of data quality in advancing translational and pre-clinical research.
  • You are collaborative, adaptable, and able to operate effectively in a fast-paced, matrixed environment.

Responsibilities
  • Serve as a primary scientific and programmatic liaison among government stakeholders, investigators, data managers, partner organizations, and internal scientific and technical teams.
  • Support the Principal Investigator and Program Manager in coordinating project activities, timelines, deliverables, priorities, risks, dependencies, and action items across scientific, data quality, communications, and technical workstreams.
  • Lead or facilitate recurring meetings, scientific working groups, requirements-gathering sessions, and stakeholder discussions, documenting decisions, action items, and follow-up activities.
  • Coordinate the development, implementation, and maintenance of data standards, metadata models, and data management approaches for exploratory, preclinical, translational, and related biomedical research data.
  • Develop and promote data management, access, and sharing practices consistent with FAIR data principles, NIH expectations, and applicable public repository requirements.
  • Translate scientific priorities and user needs into clear requirements and recommendations for data quality, informatics, software development, analytics, and AI-enabled tools.
  • Coordinate technical assistance and collaboration between scientific subject matter experts and technical teams to support investigators, data managers, and other members of the program's user community.
  • Support scientific communications, outreach, and program activities, including annual meetings, conferences, webinars, presentations, websites, and stakeholder-facing materials.
  • Coordinate with data quality and scientific staff to help track data submission review activities, recurring issues, process improvement opportunities, and related documentation needs.
  • Draft and review contract status reports, progress updates, meeting summaries, and other program deliverables that communicate project status, accomplishments, and upcoming priorities.

Requirements
  • Master's degree in a life science, biomedical science, or related scientific discipline; equivalent experience may be considered.
  • Background supporting biomedical, translational, infectious disease, vaccine, preclinical research, or scientific data-focused programs.
  • Proven ability to facilitate scientific meetings, working groups, requirements-gathering sessions, and stakeholder discussions.
  • Working knowledge of scientific research workflows, research documentation, data quality concepts, and biomedical or public health data environments.
  • Ability to translate scientific needs into data standards, data management processes, technical requirements, or program recommendations.
  • Demonstrated success coordinating complex projects, tracking action items and deliverables, maintaining documentation, and collaborating across scientific, technical, analytical, communications, and project management teams.
  • Excellent verbal and written communication skills, with the ability to summarize information clearly and professionally for different audiences.
  • Strong organizational skills, attention to detail, and ability to manage multiple priorities in a fast-paced environment.

Preferred Qualifications
  • PhD in a life or biomedical science discipline, particularly biology, microbiology, immunology, virology, infectious disease research, or a related field.
  • Prior work with NIH, HHS, NIAID, or another federal health agency.
  • Background supporting a Data Coordinating Center or a large multi-center scientific research consortium.
  • Advanced subject-matter knowledge in infectious disease, immunology, virology, vaccine development, translational science, or pre-clinical research.
  • Familiarity with biomedical data standards, data quality processes, research data management, FAIR data principles, and NIH data sharing expectations.
  • Experience coordinating scientific communications, outreach activities, conferences, or stakeholder engagement efforts.
  • Ability to provide scientific requirements or subject matter guidance for informatics, software, analytics, AI, or machine-learning initiatives.
  • Understanding of Agile practices within a software development or data management environment.

Digital Infuzion does not discriminate in employment on the basis of race, color, religion, sex (including pregnancy and gender identity), national origin, political affiliation, sexual orientation, marital status, disability, genetic information, age, membership in an employee organization, retaliation, parental status, military service, or other non-merit factor per Federal laws.
We can provide reasonable accommodation to applicants with disabilities. If you need a reasonable accommodation for any part of the application and hiring process, please contact Talent Acquisition at careers@digitalinfuzion.com. The decision on granting reasonable accommodation will be made on a case-by-case basis.

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