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Systimmune

EDC Programmer

Redmond, WA · On-site

$100K - $150K/yr

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 ...

SystImmune, Inc

EDC Programmer

Redmond, WA · On-site

$100K - $150K/yr

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 ...

Immunome, Inc.

Senior EDC Programmer

Bothell, WA · On-site

$115K - $150K/yr

Position Overview The Senior EDC (Electronic Data Capture) Programmer (Sr. EDCP) is responsible for leading the design, development, and maintenance of clinical trial databases in an EDC system. This ...

EDC

Superintendent

Midlothian, VA · On-site

About EDC EDC is one of the most respected construction companies in the country, with a geographic reach that covers the entire Eastern United States. EDC's diverse expertise in project types ...

Allied Universal

Trainer - Windsor EDC

Windsor, CT · On-site

EDC Trainer, Imprinter, and Instructor. This role will be responsible for working across these functions, ensuring the highest standards of canine explosive detection training. This individual will ...

Allied Universal

Trainer - Windsor EDC

Windsor, CT

EDC Trainer, Imprinter, and Instructor. This role will be responsible for working across these functions, ensuring the highest standards of canine explosive detection training. This individual will ...

AbbVie

Senior EDC Lead

North Chicago, IL

Veeva EDC technical study build experience is a plus. In-depth knowledge of clinical trial process. In-depth knowledge of CDASH (Required) and SDTM. Demonstrated performance as a key contributor to ...

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How much do edc jobs pay per hour?

As of Jun 12, 2026, the average hourly pay for edc in the United States is $25.14, according to ZipRecruiter salary data. Most workers in this role earn between $20.43 and $28.85 per hour, depending on experience, location, and employer.

What are some common challenges faced by EDC (Electronic Data Capture) professionals in clinical research, and how can they be managed?

Professionals working with Electronic Data Capture (EDC) systems in clinical research often encounter challenges such as ensuring data accuracy, maintaining regulatory compliance, and managing system updates. These challenges can be managed by staying up-to-date with industry regulations, participating in ongoing training, and collaborating closely with clinical teams to streamline data entry processes. Regular communication with IT and data management teams is also crucial to address technical issues promptly and ensure smooth workflows.

What are the key skills and qualifications needed to thrive as an EDC (Electronic Data Capture) Specialist, and why are they important?

To thrive as an EDC Specialist, you need a solid understanding of clinical data management, data integrity principles, and experience with electronic data capture in clinical trials, often supported by a degree in life sciences or related fields. Familiarity with EDC systems like Medidata Rave or Oracle InForm, and certifications such as CDISC or GCP, are typically required. Attention to detail, problem-solving, and strong communication skills help you effectively collaborate with clinical teams and ensure high-quality data collection. These skills are crucial for accurate, compliant data management, which underpins the success of clinical research projects.

What are EDCs?

EDC stands for 'Everyday Carry.' In the context of jobs, an EDC typically refers to the essential tools, gadgets, or items that someone carries daily to be prepared for work or emergencies. This can include multitools, flashlights, pocket knives, pens, and other items tailored to the individual's profession or needs. People in security, law enforcement, medical fields, or even office environments often have different EDC items. The concept emphasizes practicality, preparedness, and efficiency in daily tasks.
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Edc jobs near you
Infographic showing various Edc job openings in the United States as of June 2026, with employment types broken down into 86% Full Time, 10% Part Time, and 4% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $52,281 per year, or $25.1 per hour.
EDC Programmer

EDC Programmer

Systimmune

Redmond, WA • On-site

$100K - $150K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 5 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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