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

T Rowe Price

Biotech Associate

Baltimore, MD · Hybrid

Diverse responsibilities on the biotechnology investment team, including analyzing preclinical and clinical data across all therapeutic areas, accessing market potential, and developing financial ...

T Rowe Price

Bio Tech Associate

Baltimore, MD · Hybrid

Diverse responsibilities on the biotechnology investment team, including analyzing preclinical and clinical data across all therapeutic areas, accessing market potential, and developing financial ...

Deloitte

Senior Manager Data Lead

Baltimore, MD · Hybrid

Healthcare Provider L65 - Associate Vice President, AI and Data Solutions - Data Lead Join our AI ... Clinical data exchange and coding standards, including HL7, FHIR, and ICD * Data operations (ie ...

Cape Fox SS

Research Nurse

Baltimore, MD · On-site

$45 - $50/hr

Knowledge of clinical research data collection and clinical data report preparation. Working ... Associate's degree in Nursing with current state nursing license Minimum of 2 years of nursing ...

Cape Fox Shared Services

Research Nurse

Baltimore, MD · On-site

$45 - $50/hr

Performs clinical data interpretation and evaluates and interprets protocol and clinical trial ... Associate's degree in Nursing with current state nursing license. * Minimum of 2 years of nursing ...

Cape Fox Corporation

Research Nurse

Baltimore, MD · On-site

$45 - $50/hr

Performs clinical data interpretation and evaluates and interprets protocol and clinical trial ... Associate's degree in Nursing with current state nursing license. * Minimum of 2 years of nursing ...

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Clinical Data Associate information

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$13

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$86

How much do clinical data associate jobs pay per hour?

As of Aug 28, 2026, the average hourly pay for clinical data associate in Baltimore, MD is $38.70, 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.

More about Clinical Data Associate jobs

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Clinical Data Associate jobs near you
Infographic showing various Clinical Data Associate job openings in Baltimore, MD as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, and 3% Contract. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution, with an average salary of $80,505 per year, or $38.7 per hour.

Clinical Medical Review Nurse

Baltimore, MD • On-site

Lumen Solutions Group Inc.
See more jobs at Lumen Solutions Group Inc.external

Other

Posted 17 days ago

Job description

Clinical Medical Review Nurse

We are seeking Licensed Practical Nurses (LPN) or Registered Nurses (RN) to join the Quality team as Clinical Medical Review Nurses. This is a hybrid contract position requiring both remote work and regular onsite presence at the Canton, MD office. Nurses will support the review and abstraction of medical records to ensure accuracy and compliance with quality standards.

Key responsibilities include:

  • Review and abstract data from medical records
  • Extract relevant clinical data using Electronic Medical Record (EMR) systems
  • Participate in periodic onsite provider visits (minimum once per month) to retrieve medical records
  • Attend mandatory in-person training in January and again in June or July
  • Use basic Excel to enter, track, and manage clinical data
  • Work collaboratively with internal QA and clinical teams

Qualifications:

  • Active RN, LPN, or Compact Nursing License (must be current and in good standing)
  • Minimum 5 years of clinical experience
  • Experience with medical record review and data abstraction
  • Proficiency with Electronic Medical Record (EMR) systems
  • Basic knowledge of Microsoft Excel
  • Must reside in the state of Maryland (MD)
  • Willingness to be onsite 2–3 days/week in Canton, MD and travel to provider offices as needed

Preferred qualifications:

  • HEDIS experience (preferred but not required)
  • Nursing degree (Associate or Bachelor's – a plus)

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