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Full Time Edc Programmer Jobs (NOW HIRING)

Our interdisciplinary team spans human genetics, clinical science, data science and engineering ... Manage EDC build, CRF development, and data reconciliation throughout study lifecycle * Oversee ...

Systems Analyst 3

Austin, TX · On-site

$144.24/hr

Applications/Software Development Full Time NTE Rate:$144.24 I. DESCRIPTION OF SERVICES Texas ... Additional job details and special considerations Contractor will support Data Engineering and Data ...

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Full Time Edc Programmer information

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How much do full time edc programmer jobs pay per hour?

As of May 30, 2026, the average hourly pay for full time edc programmer in the United States is $39.54, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $51.44 per hour, depending on experience, location, and employer.

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

To thrive as a Full Time EDC Programmer, you need strong programming skills (often in languages like SQL, Python, or SAS), a solid understanding of clinical data management, and typically a degree in computer science or a related field. Familiarity with Electronic Data Capture (EDC) systems such as Medidata Rave or Oracle InForm, and certifications in clinical data management or EDC platforms, are highly beneficial. Attention to detail, problem-solving abilities, and effective communication skills help ensure accurate data handling and collaboration with cross-functional teams. These skills are vital for ensuring high-quality clinical trial data, regulatory compliance, and the smooth operation of clinical research processes.

What are some common challenges faced by Full Time EDC Programmers during clinical trial projects?

Full Time EDC Programmers often encounter challenges such as integrating complex protocol requirements into electronic data capture (EDC) systems, ensuring data quality and regulatory compliance, and managing tight timelines. Collaboration is key, as programmers frequently work with data managers, clinical teams, and statisticians to address evolving data collection needs and troubleshoot technical issues. Staying up-to-date with evolving EDC software and regulatory standards is essential to effectively support clinical trial operations and ensure smooth data flow.

What is a Full Time EDC Programmer?

A Full Time EDC (Electronic Data Capture) Programmer is a professional who develops, configures, and maintains EDC systems used in clinical trials and research. Their main role is to design electronic case report forms (eCRFs), manage study databases, and ensure accurate data collection and validation. EDC Programmers collaborate closely with clinical teams, data managers, and statisticians to facilitate efficient and compliant data management. Working full time, they focus on supporting multiple studies, troubleshooting issues, and implementing new features or updates to the EDC system.

What is the difference between Full Time Edc Programmer vs Full Time Automation Engineer?

AspectFull Time Edc ProgrammerFull Time Automation Engineer
CredentialsProgramming certifications, technical degreesEngineering degrees, certifications in automation tools
Work EnvironmentElectronics manufacturing, R&D labsIndustrial plants, manufacturing facilities
Industry UsageElectronics, medical devices, aerospaceManufacturing, process industries

Full Time Edc Programmers focus on developing and maintaining embedded control systems for electronic devices, often working in electronics manufacturing environments. Automation Engineers design and implement automated processes in industrial settings. While both roles require technical programming skills and industry knowledge, Edc Programmers specialize in embedded systems, whereas Automation Engineers focus on process automation. The choice depends on your interest in embedded electronics versus industrial automation.

More about Full Time Edc Programmer jobs
What cities are hiring for Full Time Edc Programmer jobs? Cities with the most Full Time Edc Programmer job openings:
What are the most commonly searched types of Edc Programmer jobs? The most popular types of Edc Programmer jobs are:
What states have the most Full Time Edc Programmer jobs? States with the most job openings for Full Time Edc Programmer jobs include:
Clinical Data Analyst, Spotfire

Clinical Data Analyst, Spotfire

SystImmune, Inc

Redmond, WA • On-site

$90K - $130K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 7 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 Spotfire Clinical Data Analyst will specialize in the installation, maintenance, and development of clinical data visualizations utilizing Spotfire. This role emphasizes creating and enhancing Spotfire-based patient profiles, real-time data review dashboards, clinical metrics dashboards, and other customized visualization reports such as live TLFs. Additionally, the Analyst will collaborate closely with Clinical Data Management, Biostatistics, Clinical Science, and Clinical Operations to optimize data visualization strategies.
This position requires a full-time onsite presence at our Redmond, WA office.
Responsibilities:
  • Lead the installation, configuration, and ongoing maintenance of Spotfire for clinical data analysis and visualization.
  • Design, develop, and maintain Spotfire dashboards for patient profiles, real-time clinical data review, surveillance, metrics tracking, and other customized visualizations.
  • Develop sophisticated, interactive visualizations to support internal data review processes, surveillance, reconciliation, and reporting needs.
  • Collaborate with Clinical Data Managers, Biostatistics, Clinical Operations, and Clinical Science teams to identify requirements and translate them into effective Spotfire visualizations.
  • Manage and continually improve the Spotfire analytics environment, ensuring data integrity, accuracy, and performance.
  • Establish and maintain a Global Spotfire Library, aligning visualization standards across multiple studies and programs.
  • Train and mentor Clinical Data Managers and other stakeholders in effectively utilizing Spotfire dashboards and reports.
  • Coordinate timelines and deliverables with Clinical Data Management and other cross-functional teams to ensure visualizations meet expectations.
  • Contribute to the evaluation and implementation of new technologies and methodologies to enhance Spotfire capabilities.
  • Document visualization specifications, maintain clear documentation for Spotfire-related processes, and contribute to departmental SOPs.
  • Uphold industry standards including protocol compliance, ICH GCP, FDA regulations, and CDISC standards (SDTM, ADaM).

Qualifications:
  • Bachelor's degree in Biostatistics, Computer Science, Life Science, or a related field.
  • Minimum of 5 years of hands-on experience in Spotfire visualization development and administration in a clinical trial setting, preferably in oncology and hematology.
  • Expert-level proficiency in Spotfire including installation, configuration, dashboard development, data integration, scripting (IronPython, TERR, etc.) and performance optimization.
  • Strong experience developing patient profiles, real-time data review dashboards, clinical metrics dashboards, and complex reports.
  • Experience with SAS/R, SQL programming, and data manipulation.
  • Familiarity with clinical trial data standards (CDISC SDTM, ADaM), experience with TLF generation preferred.
  • Experience integrating Spotfire with clinical databases and EDC systems (e.g., Medidata RAVE, Oracle Inform, Veeva).
  • Strong organizational skills, critical thinking, and the ability to manage multiple projects simultaneously.
  • Excellent verbal and written communication skills.
  • Familiarity with regulatory guidelines including GCP, ICH, and FDA requirements.
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).

Compensation and Benefits:
The expected base salary range for this position is $90,000 - $130,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate's qualifications, experience, and skills.
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.