ZipRecruiter

Log In

1

Clinical Data Programmer Jobs (NOW HIRING)

Pharmaron

Clinical Data Manager

Somerset, NJ · On-site

$60K - $75K/yr

Ensure that data/database programming and development follow and apply CDISC or applicable standards throughout the duration of a clinical trial. * Act as the Lead Data Manager for clinical trials ...

Systimmune

Clinical Data Associate

Redmond, WA · On-site

$75K - $95K/yr

The Clinical Data Associate (CDA) supports the Clinical Data Manager in executing data management ... SAS, Python, and R programming knowledge is a plus. * Familiarity with CDISC standards (CDASH, SDTM ...

Pharmaron

Clinical Data Manager

Somerset, NJ

$60K - $75K/yr

Ensure that data/database programming and development follow and apply CDISC or applicable standards throughout the duration of a clinical trial. * Act as the Lead Data Manager for clinical trials ...

SystImmune, Inc

Clinical Data Associate

Redmond, WA · On-site

$75K - $95K/yr

The Clinical Data Associate (CDA) supports the Clinical Data Manager in executing data management ... SAS, Python, and R programming knowledge is a plus. * Familiarity with CDISC standards (CDASH, SDTM ...

Lilly

OR

This requires an in-depth understanding of data technology, data flow, data standards, database programming, normalization and testing. The Clinical Study Build Programmer will collaborate with Data ...

N-Power Medicine

Clinical Data Scientist

Redwood City, CA · On-site

$132K - $226K/yr

The ideal candidate will collaborate cross-functionally with Clinical Operations, AI Engineers, and ... Data teams to validate outputs, automate workflows, and improve data infrastructure, while ...

next page

Showing results 1-20

People also search for

All JobsClinical Data Programmer Jobs

Clinical Data Programmer information

See salary details

$69.5K

$119K

$212K

How much do clinical data programmer jobs pay per year?

As of May 31, 2026, the average yearly pay for clinical data programmer in the United States is $118,962.00, according to ZipRecruiter salary data. Most workers in this role earn between $80,000.00 and $180,000.00 per year, depending on experience, location, and employer.

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.

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 Clinical Data Programmers?

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.

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.

More about Clinical Data Programmer jobs
What cities are hiring for Clinical Data Programmer jobs? Cities with the most Clinical Data Programmer job openings:
Who are the top companies hiring for Clinical Data Programmer jobs? The top employers for Clinical Data Programmer jobs are:
What states have the most Clinical Data Programmer jobs? States with the most job openings for Clinical Data Programmer jobs include:
What job categories do people searching Clinical Data Programmer jobs look for? The top searched job categories for Clinical Data Programmer jobs are:
What are popular job titles related to Clinical Data Programmer jobs? For Clinical Data Programmer jobs, the most frequently searched job titles are:
Clinical Data Programmer jobs near you
Clinical Data Manager

Clinical Data Manager

Pharmaron

Somerset, NJ • On-site

$60K - $75K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 4 days ago

Job description

Position: Clinical Data Manager
FLSA Status: Exempt
Location: Onsite (Somerset, New Jersey)
Salary: $60,000 - $75,000
Pharmaron is a global CRO (Contract Research Organization) helping pharma and biotech companies bring new therapies to life. With over 21,000 employees worldwide across 23 locations in the US, UK and China, 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 over 780 discovery projects, 1,000+ CMC programmes, and 1,000+ 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 3,000 global customers. To learn more, visit .
Job Overview:
The Clinical Data Manager ensures the integrity, accuracy, and compliance of clinical trial data, adhering to regulatory requirements, SOPs, and data standards. Responsibilities include overseeing data quality, managing external data transfers, and ensuring database development follows CDISC or relevant standards. They lead study management activities, allocate resources, create timelines, and oversee data management tasks. Additionally, they participate in audits, communicate with stakeholders, assess risks, mentor junior staff, and lead project teams to ensure high-quality data management services aligned with client expectations.
Responsibilities:
  • Responsible for ensuring the integrity, reliability, and accuracy of clinical trial data.
  • Ensure that clinical data quality and consistency conform to applicable regulatory requirements, SOP(s), processes, and data standards.
  • Ensure that external data conforms to standards outlined in the data transfer specification.
  • Ensure all data management activities are compliant with GCP, relevant regulatory requirements, and SOP(s) of Pharmaron Clinical and/or Sponsor.
  • Ensure that data/database programming and development follow and apply CDISC or applicable standards throughout the duration of a clinical trial.
  • Act as the Lead Data Manager for clinical trials, arrange for resources and assess their workload. • Identify the work scope of the study and create a study timeline based on the clinical protocol.
  • Participate in internal/external functional meetings.
  • Oversight of all data management tasks related to a clinical trial as mandated by the scope of work.
  • Monitor the project and ensure trial deliverables meet expected timelines and quality standards.
  • Participate in internal/external audits and regulatory inspections.
  • Provide risk management assessments for data management deliverables.
  • Lead clinical data management project teams in the delivery of services to clients to ensure the provided service is consistent with client needs, expectations, and contractual obligations.

What We're Looking For:
  • Bachelor's Degree or above in clinical/pharmacy, science and technology, or related discipline preferred.
  • At least 3 years' experience within a data management role, understanding of processes including study management, vendor management, CRF design, database set-up, edit check specification, DMPs, and data cleaning activities up to and including database lock.
  • Demonstrated knowledge of GCP and other regulatory requirements for clinical trials.
  • Demonstrated knowledge of the functions and activities of clinical trials.

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 21,000 employees and operations in the U.S., the U.K. and China. 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: As part of our commitment to your well-being, we offer a comprehensive benefits package:
  • Insurance including Medical, Dental & Vision with significant employer contributions
  • Employer-funded Health Reimbursement Account
  • Healthcare & Dependent Care Flexible Spending Accounts
  • 100% Employer-paid Employee Life and AD&D Insurance, Short- and Long-Term Disability Insurance
  • 401k plan with generous employer match
  • Access to an Employee Assistance Program

How to Apply:
Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!
As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.
#LI-JF1

Apply