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Clinical Data Associate Jobs in Frederick, MD (NOW HIRING)

fedRFP

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Clinical Research Associate

Fort Detrick, MD · On-site

$77K - $87K/yr

THE ROLE Monitor DoD-sponsored clinical trials on site and remotely, protecting data quality and participant safety. Expect travel to clinical sites inside and outside the continental United States.

New

Emmes

Study Start-Up Associate II

Rockville, MD · On-site +1

$34.25 - $46.75/hr

Emmes Group is transforming the future of clinical research, bringing the promise of new medical ... such as for Data Protection, Import License etc. as required. * Helps prepare and coordinate ...

IQVIA

CRA 1, IQVIA Biotech

Rockville, MD · On-site

$71K - $145K/yr

Job Overview The Clinical Research Associate I (CRA I) plays a key role in supporting the ... This role is essential in protecting patient safety, ensuring highquality clinical data, and ...

IQVIA

CRA 1, IQVIA Biotech

Rockville, MD

$71K - $145K/yr

Job Overview The Clinical Research Associate I (CRA I) plays a key role in supporting the ... This role is essential in protecting patient safety, ensuring highquality clinical data, and ...

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Clinical Data Associate information

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How much do clinical data associate jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for clinical data associate in Frederick, MD is $38.73, according to ZipRecruiter salary data. Most workers in this role earn between $29.13 and $38.70 per hour, depending on experience, location, and employer.

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 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 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 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.

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Clinical Data Associate jobs near you

Clinical Research Associate

fedRFP

Fort Detrick, MD • On-site

$77K - $87K/yr

Contractor

Medical, Dental, Vision, Life, Retirement, PTO

Posted 3 days ago

New

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Job description

ABOUT THE PROGRAM

The Office of Regulatory Activities (ORA) provides regulatory and clinical support across the full life cycle of FDA-regulated medical products sponsored by the Department of Defense. This position supports ORA on site at Fort Detrick, Maryland, working alongside government scientists, clinicians, and regulatory professionals under the DHA Research and Development / USAMRDC enterprise.

THE ROLE

Monitor DoD-sponsored clinical trials on site and remotely, protecting data quality and participant safety. Expect travel to clinical sites inside and outside the continental United States.

WHAT YOU WILL DO

•      Perform site qualification, initiation, interim, and close-out visits, on site and remotely.

•      Develop, implement, and maintain clinical monitoring plans.

•      Perform Source Data Verification and review source documents for completeness, accuracy, and consistency.

•      Generate and resolve data queries within SOP timelines to keep study milestones on schedule.

•      Review and maintain clinical site regulatory files and prepare site initiation training.

•      Prepare clinical monitoring reports documenting activities, findings, and follow-up.

•      Document deviations and non-compliance and support CAPA implementation.

WHAT YOU NEED

•      3-6 years of clinical monitoring experience.

•      Working knowledge of 21 CFR 312, 21 CFR 812, ICH E6, and GCP.

•      Demonstrated Source Data Verification experience.

•      Willingness to travel to CONUS and OCONUS clinical sites.

•      Strong written reporting skills.

NICE TO HAVE

•      CCRA or comparable certification.

•      Experience monitoring device or biologic trials.