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Clinical Data Associate Jobs in Laurel, 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 ...

UnitedHealth Group

Associate Quality Analyst

Washington, DC · On-site +1

$60K - $107K/yr

If not, open to remote outside of these areas Position Summary As an Associate Quality Analyst on ... Your work will directly impact how clinical data is processed, integrated, and leveraged across the ...

Deloitte

Senior Manager Data Lead

Baltimore, MD · On-site

Work You'll Do As an Associate Vice President, AI and Data Solutions on the AI & Data team, you ... Clinical data exchange and coding standards, including HL7, FHIR, and ICD * Data operations (ie ...

Deloitte

Senior Manager Data Lead

Mclean, VA · On-site

Work You'll Do As an Associate Vice President, AI and Data Solutions on the AI & Data team, you ... Clinical data exchange and coding standards, including HL7, FHIR, and ICD * Data operations (ie ...

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 ...

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Clinical Data Associate information

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How much do clinical data associate jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for clinical data associate in Laurel, MD is $38.62, according to ZipRecruiter salary data. Most workers in this role earn between $29.09 and $38.61 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
Infographic showing various Clinical Data Associate job openings in Laurel, MD as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, and 2% Contract. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution, with an average salary of $80,329 per year, or $38.6 per hour.

Clinical Applications Programmer II

Pharmaron Beijing Co. Ltd.

Baltimore, MD • On-site

$60 - $70/hr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 5 days ago

Job description

Position: Clinical Applications Programmer II

Salary Range: $60,000-70,000

Location: Baltimore, MD

About Pharmaron

Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 locations in the US, UK, China, and Singapore, we support drug discovery through to manufacturing with fully integrated high-quality services.

We're proud of the impact we make and just last year, we supported 887 discovery projects, 1,100+ CMC programs, and 1,397 clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,300 global customers. To learn more, visit www.pharmaron.com.

What You'll Do

We are seeking a Clinical Systems Programmer II to support the configuration, programming, validation, and ongoing management of electronic systems used to collect, process, and analyze clinical study data. This role will work closely with Clinical Data Management, Clinical Operations, Laboratory, IT, Regulatory, project teams, and study sponsors to ensure clinical systems are designed, tested, documented, and maintained in accordance with study requirements and industry standards.

The ideal candidate combines clinical research knowledge, EDC/eSource programming experience, clinical database design, and familiarity with CDISC standards and 21 CFR Part 11 requirements. This is a hands‑on role for someone who enjoys solving complex system and data challenges while ensuring high-quality, compliant clinical data collection.

Key Responsibilities
  • Configure eSource, EDC, Laboratory Information Systems, and other clinical systems based on study protocols, laboratory manuals, pharmacy manuals, and related study documentation.
  • Create and maintain CDISC/CDASH‑compliant eCRFs, study workflows, dynamic forms, and conditional logic.
  • Program screening, inpatient, and follow‑up workflows in accordance with study protocols and source templates.
  • Develop and maintain edit checks and data validation rules using logic operators to authenticate data entered into electronic forms.
  • Utilize basic JavaScript or similar programming languages to create and modify methods, edit checks, and study‑specific functionality.
  • Develop User Acceptance Testing (UAT) documentation and support Clinical Information Specialists in completing UAT activities.
  • Troubleshoot system issues, investigate defects, and implement appropriate solutions.
  • Participate in meetings with Project Managers, clinical and laboratory leaders, and study sponsors to ensure systems capture, process, and report required study data.
  • Collaborate with Clinical Systems leadership, IT, and Regulatory teams on system upgrades, implementation timelines, and validation activities.
  • Assist with the development of templates, SOPs, training materials, and standardized practices to improve efficiency and minimize study‑specific build time.
  • Meet established programming, testing, and study implementation deadlines.
  • Maintain comprehensive documentation to support audit readiness and regulatory compliance.
  • Provide system training and ongoing technical support to subject matter experts and end users.
  • Serve as the primary systems point of contact for assigned clinical studies.
  • Work independently while collaborating effectively with the Data Management team and cross‑functional stakeholders.
  • Support compliance with Good Clinical Practice (GCP), CDISC standards, 21 CFR Part 11, and applicable clinical research requirements.
What We're Looking For Required Qualifications
  • High school diploma plus 4 years of relevant experience in at least two of the following areas; OR
  • Associate degree/equivalency (60+ college credit hours) plus 2 years of relevant experience in at least two of the following areas; OR
  • Bachelor's degree/equivalency (120+ college credit hours) plus 1 year of relevant experience in at least two of the following areas:
    • Clinical research, life sciences, public health, or related field
    • eSource or EDC study design and configuration
    • Application support
    • System validation and User Acceptance Testing
    • CDISC terminology and standards
    • JavaScript or other programming languages
Knowledge & Skills
  • Understanding of Good Clinical Practice (GCP) and clinical research processes.
  • Working knowledge of CDISC standards, including CDASH and SDTM concepts.
  • Experience designing data collection solutions that support standardized clinical trial data capture and reporting.
  • Basic proficiency with JavaScript or a similar programming language.
  • Strong analytical and critical‑thinking skills with the ability to troubleshoot complex system and data issues.
  • Strong quality‑control and testing skills.
  • Ability to analyze system requirements and evaluate how system changes may impact clinical study operations and data.
  • Excellent communication and active‑listening skills.
  • Ability to manage multiple priorities and meet programming and testing deadlines.
  • Ability to work independently and collaboratively across functional teams.
  • Strong attention to detail and commitment to data quality and regulatory compliance.
Preferred Qualifications
  • Master's degree in Computer Science, Health Informatics, Clinical Research, Data Science, or a related field.
  • Industry certifications in clinical research, data management, EDC systems, programming, or related disciplines.
  • Experience with Active Directory administration.
  • Network troubleshooting experience.Application support experience.
  • Laboratory, pharmacy, or clinical application experience.
  • Web design, programming, and/or web administration experience.
  • Experience with MySQL, PostgreSQL, Microsoft SQL, Oracle, and/or Microsoft Access.
  • Laboratory, pharmacy, or clinical management experience.
Why Pharmaron?

Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 25,000 employees and operations in the US, UK, China, and Singapore. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.

Collaborative Culture:

You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.

Benefits:
  • Comprehensive Medical, Dental & Vision Insurance with significant employer contributions
  • 401(k) Retirement Plan with generous employer matching
  • Generous Paid Time Off (PTO), Paid Sick Leave & Company Holidays to support work‑life balance
  • Employer‑funded Health Savings Account (HSA) contributions (for eligible plans), plus Healthcare & Dependent Care Flexible Spending Accounts
  • 100% Employer‑paid Employee Life Insurance, AD&D, Short‑and‑Long‑Term Disability Insurance
  • Employee Assistance Program (EAP), mental health resources, and wellness programs
  • Family‑friendly benefits, including fertility support and maternity resources
  • Professional development and career growth opportunities within a leading global CRO/CDMO

As an Equal Employment Opportunity and Aff…

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