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Clinical Programmer Jobs (NOW HIRING)

SystImmune, Inc

EDC Programmer

Redmond, WA · On-site

$100K - $150K/yr

Alongside ongoing clinical trials. SystImmune has a robust preclinical pipeline of potential cancer ... The EDC Programmer (EDCP) is a critical technical role responsible for building, configuring, and ...

Systimmune

EDC Programmer

Redmond, WA · On-site

$100K - $150K/yr

Alongside ongoing clinical trials. SystImmune has a robust preclinical pipeline of potential cancer ... The EDC Programmer (EDCP) is a critical technical role responsible for building, configuring, and ...

Atorus Research

Sr Medidata RAVE Programmer

S. or Canada Contract/Corp to Corp JOB OVERVIEW The Electronic Data Capture (EDC) Programmer is responsible for providing support in creating, deploying and maintaining clinical databases and ...

Celerion

EDC Developer / Programmer

Celerion is committed to swift, exceptional clinical research through translational medicine. Every ... Programmer . You will be responsible for administration of EDC Database including evaluation ...

Celerion

EDC Developer / Programmer

OR · Remote

Celerion is committed to swift, exceptional clinical research through translational medicine. Every ... Programmer . You will be responsible for administration of EDC Database including evaluation ...

Omni Inclusive

SAS Clinical Developer

Rahway, NJ · On-site

... clinical domain 2. Strong knowledge of SDTM 3. Create advanced SAS macros, templates, and utilities for efficient data processing 4. Act as the primary programming point of contact for ...

Yochana

Clinical SAS Developer:

Passaic, NJ · On-site

Job Title Must have 6-8 yrs of exp in clinical domain Strong knowledge of SDTM Create advanced SAS macros, templates, and utilities for efficient data processing Act as the primary programming point ...

New

Cynet Systems

Clinical SAS Developer

North Wales, PA · On-site

$43 - $48/hr

Extensive programming experience in a clinical trial environment (CRO/Pharma). * Expertise in SAS/BASE, SAS/STAT, and SAS/MACRO. * In-depth knowledge of CDISC standards and regulatory submission ...

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Clinical Programmer information

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How much do clinical programmer jobs pay per hour?

As of Jun 26, 2026, the average hourly pay for clinical programmer in the United States is $64.77, according to ZipRecruiter salary data. Most workers in this role earn between $53.61 and $73.32 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical Programmer, and why are they important?

To thrive as a Clinical Programmer, you need strong proficiency in programming languages like SAS or R, a solid understanding of clinical trial processes, and typically a degree in life sciences, computer science, or a related field. Expertise with clinical data management systems (CDMS), electronic data capture (EDC) tools, and CDISC standards such as SDTM and ADaM is often required. Attention to detail, problem-solving ability, and effective communication are vital soft skills for ensuring data accuracy and collaborating with cross-functional teams. Mastery of these skills ensures the integrity and reliability of clinical trial data, supporting regulatory compliance and successful study outcomes.

What are clinical programmers and what do they do?

Clinical programmers are professionals who design, develop, and maintain computer programs used to manage and analyze clinical trial data in the pharmaceutical and biotech industries. They work closely with data managers, statisticians, and clinical teams to ensure data accuracy and regulatory compliance. Their responsibilities often include writing programs for data cleaning, statistical analysis, and generating reports using tools like SAS or R. Clinical programmers play a key role in ensuring that clinical trial data is processed efficiently and meets industry standards.

How does a Clinical Programmer typically collaborate with biostatisticians and data managers during a clinical trial?

Clinical Programmers work closely with biostatisticians and data managers throughout the clinical trial process. They are responsible for programming data listings, tables, and figures based on statistical analysis plans provided by biostatisticians. Collaboration involves ensuring data integrity, resolving data discrepancies, and implementing database validation checks, often through regular meetings and shared documentation. This teamwork is essential for maintaining data quality and meeting regulatory requirements, making strong communication and coordination skills important in the role.

What is the difference between Clinical Programmer vs Data Manager?

AspectClinical ProgrammerData Manager
Required CredentialsBachelor's degree in life sciences, computer science, or related field; programming skills in SAS, R, or SQLBachelor's degree in health sciences, statistics, or related field; experience with data management software
Work EnvironmentCollaborates with statisticians, data managers, and clinical teams to develop and validate data reportsOversees data collection, validation, and database management for clinical trials
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, clinical research organizations

While both Clinical Programmers and Data Managers work within clinical research, Clinical Programmers primarily focus on developing data reports and programming analysis datasets, whereas Data Managers handle data collection, validation, and database management. Both roles require strong analytical skills and familiarity with clinical data standards, often working closely together to ensure data quality and integrity in clinical trials.

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Clinical Programmer jobs near you
Infographic showing various Clinical Programmer job openings in the United States as of June 2026, with employment types broken down into 33% Full Time, and 67% Contract. Highlights an 100% In-person job distribution, with an average salary of $134,731 per year, or $64.8 per hour.
EDC Programmer

EDC Programmer

SystImmune, Inc

Redmond, WA • On-site

$100K - $150K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 20 days ago

Job description

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials. SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discover and IND-enabling stages, representing cutting-edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
The EDC Programmer (EDCP) is a critical technical role responsible for building, configuring, and maintaining clinical trial databases in Medidata Rave. Sitting in the Clinical Data Management (CDM) department, the EDCP works closely with Clinical Data Managers, Biostatistics, and other cross-functional study teams, leading electronic data capture (EDC) design, programming, and implementation across all phases of clinical development (Phase I-III). As a key contributor at a fast-growing biotech, the EDC Programmer has significant ownership over database quality, standards compliance, and the continuous improvement of EDC-related processes and tooling.
This position is hybrid if based in Houston, TX or Princeton, NJ, and onsite if based in Redmond, WA.
Key Responsibilities
  • Design and build Medidata Rave studies from the ground up across Phase I, II, and III clinical trials, including eCRF design, edit check programming, and study configuration.
  • Develop custom functions in Rave to address complex data validation logic, derived fields, and conditional branching beyond standard edit check capabilities.
  • Configure and maintain Rave study components including forms, fields, matrices, data dictionaries, derivations, and custom edit checks using Rave Designer and Architect.
  • Collaborate with CDM, Biostatistics, and Clinical Science teams to translate protocol requirements and CRF specifications into technically sound EDC database designs.
  • Develop and review Database Design Documents (DBDs), CRF Completion Guidelines, Edit Check Specifications, and User Acceptance Testing (UAT) plans.
  • Lead UAT activities, including authoring test scripts, executing tests, documenting defects, and driving resolution with vendors and internal stakeholders.
  • Manage study amendments and database changes throughout the trial lifecycle, maintaining thorough documentation of all modifications in accordance with SOPs and regulatory requirements.
  • Oversee and coordinate EDC-related activities with CROs and external vendors, providing technical guidance and ensuring deliverable quality and timeline adherence.
  • Ensure compliance with CDISC/CDASH standards in EDC database design, supporting downstream SDTM mapping and data review efforts.
  • Build and configure Medidata Rave RTSM modules, including randomization schemes, stratification factors, depot/kit management, and resupply algorithms.
  • Manage integrations with third-party RTSM/IRT systems (e.g., 4G Clinical, Suvoda, YPrime, Veeva Vault RTSM), including specification development, interface testing, and ongoing operational support.
  • Support data migration, external data loads (lab, ePRO, ECG, etc.), and integration with other clinical systems as needed.
  • Contribute to the development and continuous improvement of EDC standards, templates, and best practices to support a scalable, growing clinical portfolio.
  • Participate in study team meetings, providing EDC-related updates, risk assessments, and timelines.

Requirements
  • Bachelor's degree in Life Sciences, Computer Science, Information Systems, or a related field.
  • Minimum 4+ years of hands-on experience as an EDC Programmer or Database Designer in a clinical trial environment.
  • Expert-level proficiency with Medidata Rave, including Rave Designer, Rave Architect, and Rave Studio; Rave certification preferred.
  • Demonstrated experience building clinical trial databases across Phase I, II, and III studies, including first-in-human (FIH) through late-phase pivotal trials.
  • Strong custom function development experience in Medidata Rave, including complex validation logic, multi-field derivations, and dynamic form behavior.
  • Solid understanding of CDISC/CDASH standards and their application to eCRF design and data collection.
  • Experience with the full EDC lifecycle: requirements gathering, database build, UAT, go-live, amendments, database lock, and archival.
  • Familiarity with MedDRA and WHO Drug Dictionary coding and integration with Rave.
  • Knowledge of clinical trial processes, ICH E6 GCP guidelines, and regulatory requirements (FDA, EMA).
  • Experience working with CROs and managing external vendor relationships in an EDC context.
  • Strong attention to detail and a track record of producing high-quality database builds with minimal rework.
  • Excellent written and verbal communication skills with the ability to translate technical concepts for non-technical stakeholders.
  • Ability to manage multiple studies simultaneously in a fast-paced, agile environment.
Preferred Qualifications
  • Hands-on experience building Rave RTSM studies, including randomization design, stratification, kit management, and resupply logic; and/or direct integration experience with third-party IRT/RTSM platforms (e.g., Almac, Suvoda, Bracket, Veeva Vault RTSM).
  • Familiarity with additional EDC platforms (e.g., Veeva Vault EDC, Oracle Clinical One) is a plus.
  • Experience in oncology trials (solid tumors or hematologic malignancies) strongly preferred.
  • Exposure to eSource, eConsent, or wearable/device integration.
  • SAS, R, or SQL programming experience to support data review activities.
  • Mandarin language proficiency (spoken and/or written) is a plus, given collaborative relationships with partners in China.

Compensation and Benefits:
The expected base salary range for this position is $100,000 - $150,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate's level qualifications, experience, and skills.
While most offers typically fall within the low to mid-point of the range, we may extend an offer toward the higher end for exceptional candidates whose background and expertise exceeds the requirements of the role.
SystImmune is a leading and well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company's success. SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.
We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.

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