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

VENESCO LLC

Clinical Research Associate

Frederick, MD · On-site

$100K - $110K/yr

Clinical Research Associate Venesco LLC is seeking a Clinical Research Associate (CRA) to provide ... Perform source data verification (SDV). * Review informed consent documentation and study records.

Axle

Associate Director of AI and Data

Rockville, MD · On-site

$60K - $60K/yr

They are seeking a visionary Associate Director of Artificial Intelligence, Modeling, and Data to ... clinical trial design. • Optimize MLOps and DevSecOps processes to ensure the rapid, secure ...

Axle

Associate Director of AI and Data

Rockville, MD · On-site

They are seeking an Associate Director of Artificial Intelligence, Modeling, and Data to lead the ... clinical research. Responsibilities : • Architect and execute a comprehensive AI/ML strategy that ...

Emmes

Clinical Research Associate I

Rockville, MD · On-site

Through our two business units- Emmes, a full-service CRO , and Veridix AI, our technology, data ... The Clinical Research Associate (CRA) I is responsible for monitoring clinical study sites either ...

Emmes

Clinical Research Associate II

Rockville, MD · Hybrid

Through our two business units- Emmes, a full-service CRO , and Veridix AI, our technology, data ... The Clinical Research Associate (CRA) II is responsible for monitoring clinical study sites either ...

REGENXBIO

In-House CRA / Clinical Trial Associate

Rockville, MD · On-site

$34.25 - $46.75/hr

As the In-house CRA you will support and coordinate the logistical aspects of clinical trial management, site management, data review and cleaning according to FDA regulations, Good Clinical Practice ...

REGENXBIO

In-House CRA / Clinical Trial Associate

Rockville, MD · On-site

$34.25 - $46.75/hr

As the In-house CRA you will support and coordinate the logistical aspects of clinical trial management, site management, data review and cleaning according to FDA regulations, Good Clinical Practice ...

Emmes

Study Start-Up Associate II

Rockville, MD · Remote

$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

$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 · 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 ...

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Showing results 21-40

All JobsClinical Data Associate JobsClinical Data Associate Jobs in Frederick, MD

Clinical Data Associate information

See Frederick, MD salary details

$13

$38

$86

How much do clinical data associate jobs pay per hour?

As of Aug 12, 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 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
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Clinical Data Associate jobs near you

Clinical Research Associate

VENESCO LLC

Frederick, MD • On-site

$100K - $110K/yr

Full-time

Posted 17 days ago

Job description

Description:

Clinical Research Associate


Venesco LLC is seeking a Clinical Research Associate (CRA) to provide clinical monitoring and oversight support to ensure studies are conducted in compliance with protocols, Good Clinical Practice (GCP), FDA regulations, ICH guidelines, and sponsor requirements.


Requirements:

Duties and Responsibilities

  • Conduct site qualification, initiation, monitoring, and closeout visits.
  • Perform source data verification (SDV).
  • Review informed consent documentation and study records.
  • Evaluate protocol compliance and identify deviations.
  • Review regulatory binders and essential documents.
  • Generate clinical monitoring reports and follow-up letters.
  • Support site training and communication activities.
  • Track and assist with CAPA implementation.
  • Support audit and inspection readiness.
  • Maintain study documentation and monitoring files.

Minimum Qualifications

  • Bachelor's degree in Life Sciences, Nursing, Public Health, or related discipline.
  • Minimum 3 years of clinical monitoring experience.
  • Knowledge of FDA regulations, ICH-GCP, and clinical research practices.
  • Strong written and verbal communication skills.
  • Ability to travel CONUS and OCONUS.


Venesco, LLC, is an equal opportunity and affirmative action employer. Venesco is committed to administering all employment and personnel actions on the basis of merit and free of discrimination based on race, ethnicity, religious affiliation, gender, gender identity or expression, sexual orientation, national origin, protected veteran status, or status as an individual with a disability. Consistent with this commitment, we are dedicated to the employment and advancement of qualified minorities, women, individuals with disabilities, protected veterans, persons of all ethnic backgrounds and religions according to their abilities.

For more information on Venesco, LLC., visit https://venesco.com.