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Clinical Data Associate Jobs in Silver Spring, MD

EDJ Associates,

Health IT Manager I

Washington, DC · Hybrid

$107K - $131K/yr

Employment is contingent upon EDJ Associates, Inc. receiving a contract award. This position is ... • Support data policy and process implementation for cancer research and clinical care ...

EDJ Associates,

Health IT Manager I

Washington, DC · On-site

$107K - $131K/yr

Employment is contingent upon EDJ Associates, Inc. receiving a contract award. This position is ... • Support data policy and process implementation for cancer research and clinical care ...

Emmes

Senior Clinical Research Associate

Rockville, MD · On-site +1

Overview Senior Clinical Research Associate US Remote Emmes Group: Building a better future for us ... As part of the site visits, independently conducts Informed Consent (ICF) review, source data ...

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All JobsClinical Data Associate JobsClinical Data Associate Jobs in Silver Spring, MD

Clinical Data Associate information

See Silver Spring, MD salary details

$14

$40

$89

How much do clinical data associate jobs pay per hour?

As of Jun 22, 2026, the average hourly pay for clinical data associate in Silver Spring, MD is $40.14, according to ZipRecruiter salary data. Most workers in this role earn between $30.24 and $40.14 per hour, depending on experience, location, and employer.

What are some common challenges faced by Clinical Data Associates when ensuring data quality during clinical trials?

Clinical Data Associates often encounter challenges such as identifying and resolving discrepancies in large datasets, maintaining strict compliance with regulatory standards, and coordinating timely data entry from multiple sites. They must work closely with clinical research teams and data managers to clarify ambiguous data and implement data cleaning procedures. Staying organized and detail-oriented is essential to ensure data accuracy and the successful progression of clinical trials.

What are the key skills and qualifications needed to thrive as a Clinical Data Associate, and why are they important?

To thrive as a Clinical Data Associate, you need a solid understanding of clinical research, data management principles, and attention to detail, often supported by a degree in life sciences or a related field. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of regulatory guidelines like GCP or CDISC is typically required. Strong organizational skills, analytical thinking, and clear communication set outstanding candidates apart in this role. These skills ensure the accuracy, integrity, and compliance of clinical trial data, which are crucial for successful research outcomes and regulatory approval.

What does a Clinical Data Associate do?

A Clinical Data Associate is responsible for collecting, validating, and managing clinical trial data to ensure its accuracy, completeness, and compliance with regulatory standards. They work closely with clinical research teams to monitor data quality, resolve discrepancies, and prepare data for analysis. Their work is essential in supporting drug development and regulatory submissions by ensuring reliable and high-quality clinical data.

What Does a Clinical Data Associate Do?

A clinical data associate is responsible for tracking data and results in a research study. As a clinical data associate, your job duties are to collect data, perform data management, and input data into any software used by your team. You work on a research team, so you must be able to work collaboratively and have excellent organizational skills. While you spend most of your time in an office, you may be required to work in the field to record data. The only universal qualifications needed for this career are a background in health care or medical science research and experience with data management software like Oracle Clinical, Microsoft Excel, and SPSS.

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

AspectClinical Data AssociateClinical Research Coordinator
Primary RoleManage and ensure accuracy of clinical trial dataOversee trial operations, patient recruitment, and site management
CredentialsBachelor's in life sciences or related field; familiarity with data managementBachelor's in health sciences or related field; clinical trial experience
Work EnvironmentData management teams, clinical trial databasesClinical sites, hospitals, research facilities
Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites

While both roles support clinical trials, a Clinical Data Associate primarily focuses on managing and validating trial data, ensuring accuracy and compliance. In contrast, a Clinical Research Coordinator handles the overall trial operations, including patient recruitment and site coordination. Both roles require relevant certifications and work within the clinical research industry, but their daily responsibilities differ significantly.

More about Clinical Data Associate jobs
What are the most commonly searched types of Clinical Data jobs in Silver Spring, MD? The most popular types of Clinical Data jobs in Silver Spring, MD are:
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What job categories do people searching Clinical Data Associate jobs in Silver Spring, MD look for? The top searched job categories for Clinical Data Associate jobs in Silver Spring, MD are:
What cities near Silver Spring, MD are hiring for Clinical Data Associate jobs? Cities near Silver Spring, MD with the most Clinical Data Associate job openings:
Clinical Data Associate jobs near you
Infographic showing various Clinical Data Associate job openings in Silver Spring, MD as of June 2026, with employment types broken down into 77% Full Time, 15% Part Time, and 8% Contract. Highlights an 92% In-person, and 8% Hybrid job distribution, with an average salary of $83,501 per year, or $40.1 per hour.
Health IT Manager I

Health IT Manager I

EDJ Associates,

Washington, DC • Hybrid

$107K - $131K/yr

Full-time

Posted 28 days ago

Job description

Description

CONTINGENT HIRE NOTICE: This position is a contingent hire. Employment is contingent upon EDJ Associates, Inc. receiving a contract award. This position is performed primarily on-site at NIH headquarters in Bethesda, Maryland. Applicants must be able to obtain and maintain a security clearance from the federal government.
The Health IT Manager I oversees task groups and provides technical authority within the CTRO and Clinical Trials Reporting Program (CTRP). This role directs analysts and programmers, leads system problem-solving with new technology, provides on-site technical direction, and coordinates across CBIIT programs to ensure effective delivery of biomedical informatics services.

Key Responsibilities
•        Monitor the performance of each task or group of tasks and inform the Program Manager of all problems and accomplishments.
•        Serve as the technical authority for specific task areas and participate in the resolution of systems problems with new technology.
•        Direct systems analysts, programmers, and other technical personnel on assigned work.
•        Coordinate across CBIIT programs and with NCI Divisions, Offices, and Centers.
•        Provide on-site and remote technical direction as necessary.
•        Support the identification and implementation of project management tools to meet program needs.
•        Assist with the development, maintenance, and document control of project plans, roadmaps, and contract deliverable documents.
•        Support data policy and process implementation for cancer research and clinical care initiatives.
•        Provide consulting and technical support to government project and task managers.
•        Support end-user help desk and other technical services as directed by the COR.

Skills, Knowledge and Expertise
•        Minimum of three (3) years of experience in health IT management or a related discipline.
•        Demonstrated ability to direct technical teams and manage complex IT projects.
•        Strong problem-solving and decision-making skills.
•        Knowledge of biomedical informatics, clinical trial systems, and NCI processes preferred.
•        Experience evaluating AI/NLP tools for clinical data workflows preferred
•        Experience with federal government contract management and reporting.
•        Ability to obtain and maintain a Level 1 (Non-Sensitive) NACI background investigation.
•        Project Management Professional Certification (PMP) a plus.

Tools and Technologies:

•        Microsoft Office Suite (Word, Excel, PowerPoint)
•        Project management and issue tracking tools
•        ServiceNow or similar ticketing systems