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Edc Programmer Jobs in California (NOW HIRING)

MiniMed

Sr Clinical IT Developer

Los Angeles, CA · On-site

About the Role MiniMed is looking for a Clinical Database Developer who is responsible and ... Veeva EDC or Oracle EDC or other smaller systems) and clinical trial management systems.

Numentica LLC

Senior Data Engineer

San Diego, CA · On-site

$114K - $155K/yr

Experience with Veeva, LIMS, ELN/Benchling, CTMS, EDC, MasterControl, or HRIS integrations. * Experience with AI/ML workloads on a lake-house. * Microsoft Fabric Data Engineering certification.

Numentica LLC

Senior Data Engineer

San Diego, CA

$40 - $65/hr

Experience with Veeva, LIMS, ELN/Benchling, CTMS, EDC, MasterControl, or HRIS integrations. * Experience with AI/ML workloads on a lake-house. * Microsoft Fabric Data Engineering certification.

Collabera

Clinical Project Manager

Santa Clara, CA · On-site

... RAVE EDC, DS Navigator, SAS Programming, Reporting and Analytics, Siebel CTMS, Documentum Qualifications equirements BA or BS degree in technical or scientific discipline required. 8+ years of ...

Collabera

Clinical Data Manager

Irvine, CA · On-site

Perform data management activities on both Electronic Data Capture (EDC) and paper studies. Major ... Work closely with clinical project team and database programmers to provide edit check requirements ...

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How much do edc programmer jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for edc programmer in California is $39.02, according to ZipRecruiter salary data. Most workers in this role earn between $25.38 and $50.77 per hour, depending on experience, location, and employer.

What is an EDC programmer?

An EDC (Electronic Data Capture) Programmer is responsible for designing, developing, and maintaining clinical trial databases used to collect and manage study data. They work with electronic data capture systems, ensuring that case report forms (CRFs) are correctly configured and meet study requirements. EDC Programmers collaborate with clinical data managers, biostatisticians, and regulatory teams to ensure compliance with industry standards and protocols. Their role is crucial in improving data accuracy, integrity, and efficiency in clinical research.

What are the typical daily responsibilities of an EDC programmer in a clinical trials environment?

As an EDC Programmer, your daily responsibilities often include designing and configuring electronic case report forms (eCRFs), managing database setup, performing system validations, and troubleshooting data discrepancies. You’ll collaborate closely with clinical data managers, biostatisticians, and study coordinators to ensure the system effectively supports trial protocols and regulatory requirements. Additionally, you may be responsible for providing user support and training, handling database updates, and participating in ongoing process improvements. This role is central to maintaining high data quality and supporting the operational success of clinical trials.

What are the key skills and qualifications needed to thrive as an EDC programmer, and why are they important?

To thrive as an EDC Programmer, you need strong programming skills, particularly in database management systems and clinical data standards, often supported by a degree in computer science or a related field. Experience with electronic data capture (EDC) platforms such as Medidata Rave, REDCap, or Oracle InForm, as well as knowledge of CDISC standards, is highly valued. Attention to detail, effective communication, and problem-solving abilities are key soft skills for success in this role. These competencies are essential for ensuring accurate clinical trial data capture and smooth collaboration with study teams in regulated environments.

What are the most commonly searched types of Edc Programmer jobs in California?

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For Edc Programmer jobs in California, the most frequently searched job titles are:

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Edc Programmer jobs near you
Infographic showing various Edc Programmer job openings in California as of August 2026, with employment types broken down into 91% Full Time, and 9% Contract. Highlights an 74% In-person, and 26% Remote job distribution, with an average salary of $81,158 per year, or $39 per hour.

Sr. Statistical Programmer

Kodiak Sciences Inc.

Palo Alto, CA • On-site

Full-time

Re-posted 3 days ago

Job description

Kodiak Sciences Inc. is a rapidly growing, clinical-stage biopharmaceutical company dedicated to transforming ophthalmology through innovative therapeutics. Our proprietary Antibody Biopolymer Conjugate Drug (ABCD) platform integrates protein engineering, polymer chemistry, small molecule drug discovery, and advanced drug delivery technologies to address prevalent and debilitating retinal diseases with the goal of improving patient outcomes worldwide. In this fast-growing and fast-paced organization, your expertise is needed to provide support for clinical and statistical programming activities related to multiple clinical studies.

Key Responsibilities

  • Assist in the review of key study-related documents produced by other functions, e.g. Statistical Analysis Plan, Case Report Forms, Data Management Plan, Database Specifications, EDC Data Structures, DMC plans and other clinical documents
  • Write, test and validate SAS programs to produce analysis datasets, TLFs, to be included in reports for submission to regulatory agencies, publications and other communications as needed
  • May serve as a technical lead and project manager for multiple studies managing all aspects of study deliverables related to statistical and clinical programming as needed
  • Work with internal stakeholders to gather requirements and write specifications
  • Interact and communicate with Statisticians, Data Managers, Clinical Operations, Medical Monitors, Medical Writing and Medical Monitors to address programming related study deliverables
  • Write macros for reusability
  • Review and verify vendor deliverables for quality and accuracy
  • Contribute to the development review of Statistical Programming policies, standard operating procedures and other controlled documents
  • Interface with outsourcing partners and vendors

Education & Experience

  • B.S. preferably in Mathematics, statistics, computer sciences or other related field
  • 5+ years of clinical trials experience in pharmaceutical or biopharmaceutical setting or equivalent

Additional Skills

  • Thorough knowledge of the drug development and regulatory submission cycle
  • Excellent project management skills
  • Excellent communication skills
  • Able to work in a fast pace and agile environment
  • In-depth and current knowledge of regulatory requirements and guidance
  • Excellent SAS and CDISC skills
  • Proficiency in MS Word, Excel, PowerPoint, and Project

Apply