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Full Time Edc Programmer Jobs in Seattle, WA (NOW HIRING)

Clinical Data Associate

Redmond, WA · On-site

$75K - $95K/yr

This role is full-time onsite in Redmond, WA. Please note that SystImmune plans to relocate to a ... programming errors under CDM guidance. * Perform UAT (User Acceptance Testing) of EDC systems and ...

Clinical Data Associate

Redmond, WA · On-site

$75K - $95K/yr

This role is full-time onsite in Redmond, WA. Please note that SystImmune plans to relocate to a ... programming errors under CDM guidance. * Perform UAT (User Acceptance Testing) of EDC systems and ...

Clinical Data Manager

Redmond, WA · On-site

$100K - $170K/yr

This position requires you to be onsite full-time in Redmond, WA.Responsibilities: * Leads all DM ... Experience working within a Clinical EDC system (e.g., Medidata Rave, Veeva EDC). * SAS programming ...

Clinical Data Manager

Redmond, WA · On-site

$100K - $170K/yr

This position requires you to be onsite full-time in Redmond, WA. Responsibilities:  * Leads all ... Experience working within a Clinical EDC system (e.g., Medidata Rave, Veeva EDC). * SAS programming ...

This position is full-time onsite and can work out of our Redmond, WA or Princeton, NJ locations ... Expertise with EDC systems, external data integrations, data reconciliation, and database ...

This position requires a full-time onsite presence at our Redmond, WA office. Responsibilities ... Experience with SAS/R, SQL programming, and data manipulation. * Familiarity with clinical trial ...

Full Time Edc Programmer information

See Seattle, WA salary details

$13

$44

$78

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

As of Jul 16, 2026, the average hourly pay for full time edc programmer in Seattle, WA is $44.99, according to ZipRecruiter salary data. Most workers in this role earn between $29.28 and $58.56 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 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 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 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.

What are the most commonly searched types of Edc Programmer jobs in Seattle, WA? The most popular types of Edc Programmer jobs in Seattle, WA are:
What cities near Seattle, WA are hiring for Full Time Edc Programmer jobs? Cities near Seattle, WA with the most Full Time Edc Programmer job openings:
Clinical Data Associate

Clinical Data Associate

Systimmune

Redmond, WA • On-site

$75K - $95K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 10 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 Clinical Data Associate (CDA) supports the Clinical Data Manager in executing data management activities across clinical trials, with a primary focus on Phase 3 and other large-scale studies. The CDA will gain hands-on experience across the full DM lifecycle while working under the guidance of senior data management staff.
 

This role is full-time onsite in Redmond, WA. Please note that SystImmune plans to relocate to a new facility in Bothell, WA in the fall.


Responsibilities: 
  • Support the CDM in day-to-day data management activities across study start-up, maintenance, and close-out, including tracking open queries and data cleaning timelines.
  • Assist in the development and review of DM documents such as Data Management Plans, CRF Completion Guidelines, and data review plans using established templates and standards.
  • Perform data review activities including query generation, query resolution follow-up, and non-system edit check output review under CDM oversight.
  • Assist with SAE reconciliation and non-CRF data reconciliation activities, escalating issues to the CDM as appropriate.
  • Support medical coding activities using MedDRA and WHO Drug dictionaries, coordinating with the CDM and CRO for medical review.
  • Run and review SAS and/or R programs and data listings as directed; assist in troubleshooting basic programming errors under CDM guidance.
  • Perform UAT (User Acceptance Testing) of EDC systems and edit checks per provided specifications and test scripts.
  • Assist in tracking and coordinating CRO/vendor deliverables, flagging risks or delays to the CDM.
  • Contribute to data quality monitoring by reviewing metrics reports and flagging trends or anomalies to the CDM.
  • Support database lock activities by assisting with lock checklists, outstanding query resolution, and coordination tasks.
  • Participate in the development and review of DM SOPs and process improvement initiatives.
  • All other duties as assigned.

Qualifications:
  • BA or BS in life sciences, health informatics, or a related field.
  • 1–3 years of relevant clinical data management or clinical research experience; equivalent internship or co-op experience in a clinical or pharma setting will be considered.
  • Exposure to a Clinical EDC system (e.g., Medidata Rave, Veeva EDC) preferred.
  • SAS, Python, and R programming knowledge is a plus.
  • Familiarity with CDISC standards (CDASH, SDTM) and GCP guidelines preferred; willingness to develop deep knowledge required.
  • Detail-oriented with strong organizational and time management skills.
  • Effective written and verbal communication skills; ability to work cross-functionally.
  • Eagerness to learn in a fast-paced, clinical-stage biopharmaceutical environment.
  • Oncology experience or interest a plus.
 
Compensation and Benefits:
The expected base salary range for this position is $75,000 - $95,000 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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