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Clinical Research Data Manager Jobs in Reston, VA

Cape Fox Corporation

Clinical Research Coordinator

Bethesda, MD · On-site

$26 - $34.50/hr

... data acquisition and analysis using a variety of methods, including recruitment, entry, management ... Clinical Research, and the Empirical Research Lab. Supports the collection of data from patient ...

Cape Fox SS

Clinical Research Coordinator

Bethesda, MD

$26 - $34.50/hr

... data acquisition and analysis using a variety of methods, including recruitment, entry, management ... Clinical Research, and the Empirical Research Lab. Supports the collection of data from patient ...

Emmes

Data Manager

Rockville, MD · On-site +1

Emmes Group is transforming the future of clinical research, bringing the promise of new medical ... The Data Manager is responsible for the completeness and accuracy of the study data in the ...

asrcfh

Clinical Data Manager 2

Reston, VA · On-site

Manage the delivery of high-quality data from project start-up and planning to project execution ... research databases * Develop and extract patient clinical data reports for publications and ...

Cape Fox SS

Research Nurse

Bethesda, MD

$56/hr

... management of research subject files, copying and organizing research data. Assist in updates for clinical staff on patient care, protocol process and progress, human rights protection, ICH Good ...

Cape Fox Corporation

Research Nurse

Bethesda, MD · On-site

$56/hr

... management of research subject files, copying and organizing research data. * Assist in updates for clinical staff on patient care, protocol process and progress, human rights protection, ICH Good ...

CenExel

Clinical Research Coordinator I

Gaithersburg, MD · On-site

$26.90 - $34.35/hr

Our world-class PIs, advanced patient engagement strategies, premium data analytics, and integrated ... Crisis management and problem solving skills; ability to react calmly and effectively in emergent ...

CBH Health

Clinical Research Coordinator I

Gaithersburg, MD · On-site

$26.90 - $34.35/hr

Our world-class PIs, advanced patient engagement strategies, premium data analytics, and integrated ... Crisis management and problem solving skills; ability to react calmly and effectively in emergent ...

CenExel

Clinical Research Coordinator I

Gaithersburg, MD · On-site

$26.90 - $34.35/hr

Our world-class PIs, advanced patient engagement strategies, premium data analytics, and integrated ... Crisis management and problem solving skills; ability to react calmly and effectively in emergent ...

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All JobsClinical Research Data JobsClinical Research Data Manager JobsClinical Research Data Manager Jobs in Reston, VA

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 Jul 20, 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.

How to become a clinical research data manager?

To become a clinical research data manager, candidates typically need a bachelor's degree in health sciences, life sciences, or a related field, along with experience in clinical data management or research. Skills in database management, familiarity with electronic data capture (EDC) systems, and knowledge of regulatory requirements like GCP are essential. Certification such as the Society for Clinical Data Management (SCDM) CDMP can enhance job prospects.

How much does a Pfizer Clinical Data Manager make?

A Pfizer Clinical Data Manager typically earns between $80,000 and $120,000 annually, depending on experience, location, and level of responsibility. The role requires strong data management skills, familiarity with clinical trial software, and often a background in life sciences or healthcare. Salaries can vary based on the complexity of projects and the candidate's certifications.

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 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.

Is CRA an entry level job?

A Clinical Research Associate (CRA) is typically not an entry-level position; it usually requires prior experience in clinical research, monitoring, or related roles. Entry-level roles in clinical research often include Clinical Trial Assistants or Coordinators, with CRAs generally needing a background in life sciences, good clinical practice (GCP) training, and sometimes certification such as CCRP or RAC.

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 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 does a data manager do in clinical trials?

A clinical research data manager is responsible for collecting, organizing, and maintaining data from clinical trials to ensure accuracy, completeness, and compliance with regulatory standards. They often use data management tools like electronic data capture (EDC) systems and collaborate with research teams to support data quality and integrity throughout the study. Strong attention to detail and knowledge of Good Clinical Practice (GCP) are essential for this role.
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:
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Clinical Research Data Manager jobs near you
Infographic showing various Clinical Research Data Manager job openings in Reston, VA as of July 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $111,668 per year, or $53.7 per hour.
Clinical Research Data and Analytics Manager (Hybrid)

Clinical Research Data and Analytics Manager (Hybrid)

The Geneva Foundation

Bethesda, MD • On-site

$105K - $115K/yr

Full-time

Re-posted 8 days ago

Job description

About the Position:
The Data and Analytics Manager is responsible for leading the day-to-day functions of a core Data & Analytics team providing centralized data coordination and data analysis services for a large research portfolio. Reporting to the Senior Manager of Regulatory Affairs & Data, this role directly oversees a small, dedicated team (including a Clinical Data Manager and a Data Management Analyst) supporting a robust portfolio of 65+ active multi-site research studies, including federally funded, FDA-regulated and industry-sponsored clinical trials, across military treatment facilities, academic institutions, and other sites nationwide. This position works cross-organizationally to ensure the on-time execution of high-quality and compliant research, proper documentation of procedures, accurate data reporting, and assures real-time data access for the investigator(s) and staff.
In this dynamic position, you will manage the day-to-day data management and analysis pipeline, act as the Subject Matter Expert (SME) for internal and external stakeholders, as well as execute on your own data management, quality control (QC), and data analysis activities. A strong candidate will be a versatile professional who is equally comfortable developing and executing high-level strategy, effectively delegating and empowering their staff, and rolling up their sleeves to troubleshoot a formula, run analyses, draft/negotiate data sharing agreements, or build a database.
Work Location:
This is a hybrid - remote role supporting a program based out of the Uniformed Services University in Bethesda, MD, with research performance sites located across the continental United States. Applicants must live within a reasonable commuting distance of Bethesda, MD for on-site presence as necessary. A comprehensive government background check will be administered.
About the Program:
The Musculoskeletal Injury Rehabilitation Research for Operational Readiness (MIRROR) Program was established to support the execution of clinically relevant research to advance the care of service members with non-combat related musculoskeletal injury (MSI). Headquartered at the Uniformed Services University of the Health Sciences (USU) in Bethesda, MD, MIRROR provides coordination and support of inter-service and inter-disciplinary partnerships across military treatment facilities (MTFs), military training centers (MTCs), and civilian academic centers to execute cutting-edge research in order to mitigate the burden of MSI on military readiness. The MIRROR portfolio currently consists of 65+ active projects.
Salary Range
$105,000 - $115,000. Salaries are determined based on several factors including external market data, internal equity, and the candidate's related knowledge, skills, and abilities for the position.
This is a hybrid - remote role supporting a program based out of the Uniformed Services University in Bethesda, MD, with research performance sites located across the continental United States. Applicants must live within a reasonable commuting distance of Bethesda, MD for on-site presence as necessary. A comprehensive government background check will be administered.
Qualifications:
  • Bachelor's degree in a scientific, informatics, or relevant field required. Master's degree, equivalent work experience, or relevant professional certification strongly preferred.
  • 3-5 years' professional experience in clinical research data management, clinical trials, or a data coordinating center environment required. Previous research conduct experience highly desired.
  • 1-2 years in team management, leadership, or direct supervisory experience required.
  • Must possess a strong working knowledge of clinical research data compliance, including requirements for FDA-regulated clinical trials, IRB requirements for human subjects protections, and general best research practices.
  • Must have demonstrated experience building complex, longitudinal, multi-arm electronic clinical research databases required. Experience using REDCap is strongly preferred.
  • Must have demonstrated experience with cleaning, analyzing, and presenting real-time data and metrics.
  • Must have a strong understanding of data visualization principles and the ability to build or troubleshoot business intelligence dashboards. Experience with PowerBI strongly preferred.
  • Experience executing or navigating data agreements (e.g. data use agreements, data sharing agreements, etc.) as they pertain to data privacy and security is highly desired.
  • Must be organized, attentive to details, and possess an exceptional diplomatic and professional communication skills. Must have the ability to successfully build relationships with key stakeholders and to effectively communicate requirements for data and analytics systems as well as translate technical data requirements to non-technical stakeholders.
  • Must thrive in a fast-paced environment with shifting priorities, multiple moving targets, and strict timelines.

Management Responsibilities:
  • Supervise the day-to-day activities of assigned data management & analytics team program staff. Provide direction, address questions, and provide skills/knowledge transfer. Oversee workload and productivity.
  • Oversee clinical data management and analytical team staff in the execution of data operations, quality assurance cycles, and technical deliverables across the study portfolio while ensuring professional growth and alignment with program timelines.
  • Provide regular summaries and updates to Program Supervisor.
  • Plan and facilitate individual and team meetings.
  • Lead performance review processes for assigned data team staff.
  • In collaboration with Geneva People Operations and Program Supervisor, conduct counseling and corrective action, as appropriate.

Job Responsibilities:
  • Ensure data capture, management, sharing, and analysis compliance of assigned research.
  • Maintain oversight of data management and analysis needs across a large portfolio of clinical research studies, effectively delegating tasks and tracking project timelines.
  • Lead and mentor a team of data professionals. Act as a hands-on backstop to execute technical tasks (e.g., database builds, QC cycles, dashboard creation) during team absences or high-volume periods to ensure strict adherence to deadlines.
  • Contribute to the development, refinement, standardization, and dissemination of clinical data management workflows, SOPs, and cross-functional processes within the broader research program.
  • Serve as the primary representative and subject matter expert (SME) for the Data & Analytics Team in high-level meetings with a diverse mix of stakeholders, including program leadership, institutional leadership, partners, and industry sponsors.
  • Partner with study investigators and external collaborators to provide expert guidance on data collection strategies, data entry protocols, monitoring/QC plans, and data sharing requirements.
  • Participate in early-stage study development meetings to align data strategies with protocol requirements prior to execution.
  • Review and advise on the development of Case Report Forms (CRFs) for compliance, data integrity, and database compatibility, providing formal endorsement prior to IRB submission.
  • Oversee the drafting, application, and compliance management of Data Sharing Agreements (DSAs) and Data Use Agreements (DUAs).
  • Direct and participate in rigorous QC cycles to identify analytical anomalies and protect against the exposure of PII/PHI within research databases.
  • Support the translation of raw research data into knowledge products, including data analysis for manuscripts, abstracts, and statistical tables.
  • Oversee the design and maintenance of real-time study visualization dashboards to provide stakeholders with clear enrollment and study outcome insights.
  • Promote safety and confidentiality of research participants at all times.

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