1

Clinical Data Programmer Jobs in Philadelphia, PA

Success in this role requires strong programming and data visualization skills, along with the ability to translate complex clinical data into clear, actionable insights for both internal and ...

New

Success in this role requires strong programming and data visualization skills, along with the ability to translate complex clinical data into clear, actionable insights for both internal and ...

New

Bridge Strategy & Tech: Act as a hands-on liaison between senior stakeholders and engineering teams ... Clinical Data Standards: CDASH, SDTM, ADaM, OMOP, FHIR, HL7 * Patient Data Systems: EDC, ePRO, Labs ...

Provides strategic input to Clinical Operations, Biostatistics, Programming, and Quality on data flow, database design improvements, standards adoption, and process optimizations. * Represents DM in ...

Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Position: Oracle Programmer Location: Horsham PA Duration: 10+ Months The Safety Data Programmer is responsible for ...

Be Seen First

Facilitating and leading cross-functional data review meetings involving Clinical Operations, Biostatistics, Medical Monitoring, Programming, and other stakeholders. * Leading database amendments ...

next page

Showing results 1-20

Clinical Data Programmer information

See Philadelphia, PA salary details

$70.1K

$120K

$213.9K

How much do clinical data programmer jobs pay per year?

As of Aug 20, 2026, the average yearly pay for clinical data programmer in Philadelphia, PA is $120,043.00, according to ZipRecruiter salary data. Most workers in this role earn between $80,700.00 and $181,600.00 per year, depending on experience, location, and employer.

What is a clinical data programmer?

Clinical Data Programmers are professionals who manage, process, and analyze clinical trial data using specialized programming languages and software. They are responsible for creating and validating programs that ensure data collected during clinical studies is accurate, consistent, and ready for statistical analysis. Their work is essential to the integrity of clinical research, enabling regulatory submissions and supporting medical decision-making. Clinical Data Programmers often work closely with clinical data managers, statisticians, and other clinical research professionals.

How does a clinical data programmer typically collaborate with clinical research teams during a study?

Clinical Data Programmers work closely with clinical research associates, data managers, biostatisticians, and project managers to ensure the integrity and accuracy of clinical trial data. They often participate in study setup meetings, provide input on case report form (CRF) design, and develop programs for data validation and cleaning. Regular communication is essential to resolve any discrepancies or issues that arise during data collection and to implement mid-study changes. This collaborative environment ensures that the data is reliable and meets regulatory requirements.

What are the key skills and qualifications needed to thrive as a clinical data programmer, and why are they important?

To thrive as a Clinical Data Programmer, you need a strong background in programming (especially SAS or SQL), understanding of clinical trial data, and a degree in life sciences, statistics, or a related field. Familiarity with electronic data capture systems, CDISC standards (SDTM/ADaM), and regulatory requirements is typically expected, and relevant certifications can be advantageous. Attention to detail, analytical thinking, and effective communication are essential soft skills for ensuring data integrity and collaborating with cross-functional teams. These skills and qualifications are vital for producing accurate, regulatory-compliant datasets that support clinical research and successful drug development.

What is the difference between Clinical Data Programmer vs Clinical Data Analyst?

AspectClinical Data ProgrammerClinical Data Analyst
Required CredentialsBachelor's in Life Sciences, Biostatistics, or related field; knowledge of programming languages like SAS or RBachelor's in Statistics, Data Science, or related; strong analytical skills
Work EnvironmentClinical trial data management teams, often in CROs or pharmaceutical companiesData analysis teams, often in healthcare or research organizations
Employer & Industry UsageUsed in clinical research to prepare datasets for analysisUsed to interpret data, generate reports, and support decision-making

While both roles involve working with clinical data, Clinical Data Programmers focus on coding and preparing datasets, whereas Clinical Data Analysts interpret data and generate insights. Understanding these differences helps in choosing the right career path or job search focus.

What are popular job titles related to Clinical Data Programmer jobs in Philadelphia, PA?

For Clinical Data Programmer jobs in Philadelphia, PA, the most frequently searched job titles are:

What job categories do people searching Clinical Data Programmer jobs in Philadelphia, PA look for?

The top searched job categories for Clinical Data Programmer jobs in Philadelphia, PA are:

Infographic showing various Clinical Data Programmer job openings in Philadelphia, PA as of August 2026, with employment types broken down into 2% Internship, 82% Full Time, 7% Part Time, and 9% Contract. Highlights an 82% In-person, 2% Hybrid, and 16% Remote job distribution, with an average salary of $120,043 per year, or $57.7 per hour.

Full-time

Retirement, PTO

Posted 2 days ago

New


Job description

The American College of Radiology is a professional association serving over 40,000 members nationwide.  Consistent with the ACR’s mission to advance the practice of radiology and improve the health outcomes of the populations we serve, the ACR’s Center for Research and Innovation (CRI) has been a world leader in radiology clinical research for over 50 years.  Over this period, the CRI has conducted clinical research trials and other research projects that have transformed the practice of radiology, informed the development of clinical practice standards, led to new device approvals, and changed healthcare policy.

The CRI is the core radiology resource for NCI multicenter clinical trials involving diagnostic or therapeutic radiology.  And through active research committees in neuroradiology, cardiology, oncology, and pediatrics, the CRI has developed and delivered a diverse range of research studies in partnerships with academia and commercial sponsors.  Research studies range from prospective clinical trials to retrospective reader studies, novel imaging methods and imaging software, validation of biomarkers, radiomic feature analysis, and AI algorithm development and validation.

As a Clinical Data Manager, you will play a critical role in the design, implementation, and management of clinical trial databases and data collection systems. Working closely with investigators, project teams, and data programmers, you will help ensure the integrity, quality, and usability of study data from initiation through study completion.

As a member of the ACR team, you will:

  • Review study protocols and lead clinical data management activities during study startup.
  • Design data collection strategies aligned with protocol objectives and study endpoints.
  • Collaborate with investigators and research teams to develop metadata and data capture specifications.
  • Partner with Clinical Data Programming staff to configure and validate electronic data capture (EDC) systems.
  • Develop edit checks, web logic, and validation specifications to promote data quality and consistency.
  • Create study calendars and data collection schedules.
  • Conduct Operational Qualification (OQ) and Performance Qualification (PQ) testing of databases and study systems.
  • Develop case report form (CRF) completion guidelines and user documentation.
  • Produce standard, study-specific, and ad hoc reports to support study oversight and decision-making.
  • Define and document database modifications required to support protocol amendments and study changes.
  • Perform quality control reviews to ensure data accuracy, completeness, and regulatory compliance.
  • Serve as a trusted resource for site research staff, providing guidance on protocol requirements and data collection procedures.

Qualified candidates will possess the following:

  • 3+ years of related experience preferred.
  • Professional nursing degree/other healthcare certification/bachelor’s degree preferred.
  • Experience in a multi-modality clinical trials group or research team a plus.
  • Knowledge of CDASH/CDISC Standards a plus.
  • Experience with electronic data capture (EDC) platforms required.
  • Certified Medidata Rave® Study Builder a plus.
  • Strong attention to detail and commitment to data quality and process excellence required.
  • Excellent organizational, communication, and collaboration skills required.
  • Ability to manage multiple priorities in a fast-paced, team-oriented environment required.

If you would like to put your experience to great use in a professional team-oriented environment, please apply online. To learn more about ACR’s rewarding employee experience, culture, and benefits, visit: https://www.acr.org/About-ACR/Work-With-Us

ACR is committed to a total rewards compensation philosophy that includes base salary in addition to our full suite of comprehensive benefits.  ACR’s goal is to pay competitively and equitably.  It is typical for individuals to be hired in the entry to middle of the range for their role, and compensation decisions depend on each case’s circumstances.  A reasonable estimate of the annual compensation range for this position is 73-80k.  

ACR offers a rewarding employee experience: innovative culture, professional growth potential, competitive compensation, and an exceptional benefits package, including a defined contribution pension plan, 403(b); generous paid time off package; insurance plans with the leading providers; flexible spending; tuition reimbursement; training opportunities; and wellness reimbursement.