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Edc Programmer Jobs in California (NOW HIRING)

Lead Clinical Data Manager

San Ramon, CA · Hybrid

$164K - $219K/yr

Proficiency with common electronic data capture (EDC) and clinical data management platforms, and ... Statistical Programming, Investigational sites, and/or Clinical Research Organization with ...

Proficiency with electronic data capture (EDC) systems for entering and managing study data ... About Actalent Actalent is a global leader in engineering and sciences services and talent ...

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Edc Programmer information

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How much do edc programmer jobs pay per hour?

As of Jul 14, 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 are the key skills and qualifications needed to thrive in the Edc Programmer position, 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.

Which IT job is the highest paid?

In the IT field, roles such as Chief Information Officer (CIO), IT Director, and Cloud Architect tend to be among the highest paid, often earning six-figure salaries or more. Specialized roles like Data Scientist, Solutions Architect, and cybersecurity executives also command high compensation, especially with advanced skills and certifications in cloud platforms, security, or data analysis.

What tech jobs pay $400,000 a year?

For an EDC programmer or similar specialized tech roles, earning $400,000 annually typically requires extensive experience, advanced skills in embedded systems, and often leadership responsibilities. High-paying tech jobs at this level are usually found in senior engineering, executive, or consulting positions within technology companies or industries like aerospace, defense, or finance. Compensation may include base salary, bonuses, and stock options, especially in high-growth or large organizations.

What are some 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 is an EDC programmer?

An EDC programmer is a professional who develops and maintains electronic data capture (EDC) systems used in clinical trials and research to collect, manage, and analyze data. They typically have skills in programming languages such as SQL, SAS, or R, and work closely with data managers and clinical teams to ensure data accuracy and compliance. EDC programmers often require knowledge of regulatory standards like GCP and may hold certifications in clinical data management.

What jobs in the US pay $300,000 a year?

For an EDC programmer or similar specialized roles, annual salaries of $300,000 or more are typically found in senior or executive positions such as software engineering managers, cybersecurity directors, or senior developers with extensive experience and advanced skills. High-paying roles often require advanced certifications, leadership responsibilities, or working in high-demand industries like finance, technology, or defense. Compensation varies based on location, company size, and individual expertise.

What is an EDC Programmer job?

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 most commonly searched types of Edc Programmer jobs in California? The most popular types of Edc Programmer jobs in California are:
What cities in California are hiring for Edc Programmer jobs? Cities in California with the most Edc Programmer job openings:
Infographic showing various Edc Programmer job openings in California as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $81,158 per year, or $39 per hour.
Clinical Data Manager - Data Integrity & Investigation

Clinical Data Manager - Data Integrity & Investigation

RDI

Van Nuys, CA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 11 days ago


RDI Corporation rating

5.4

Company rating: 5.4 out of 10

Based on 20 frontline employees who took The Breakroom Quiz

48th of 72 rated call and contact centers


Job description

When a new assay disagrees with the predicate, somebody has to figure out why. Is it the test? The specimen? The site? A single keystroke at data entry? Most "data people" report the discordance and move on. We're looking for the one who treats it as a case to crack.
You'll own subject- and sample-level data across 20-30 concurrent method-comparison and specimen-collection studies - and your real job is to make sure the dataset tells the truth. Not the convenient version. Not the version that makes a result look cleaner than it is. What actually happened. You check every cell because the truth lives in the cells, and you chase every anomaly to root cause because "looks off" is where the work starts.
Own the data. Find the true story it's hiding.
What this role actually is
  • Investigation - you trace discordant results, outliers, and drift to their source and determine whether you're looking at real signal or a data artifact.
  • Source-level verification - every critical field traced to origin; you're the one who finds the single transcription error in 10,000 rows.
  • Reconciliation - lab results, sample inventory, demographics, and visit dates agree across systems, or you find out why.
  • Telling it straight - you can stand in front of the science and regulatory team and explain what the data means, honestly - and hold the line when someone wants a prettier story than the data supports.
  • Database lock - you're accountable for the dataset that goes to FDA, and you'll defend every value in it under audit.
  • ALCOA+ / 21 CFR Part 11 - integrity isn't a checkbox here, it's the whole job.

How you'll work
  • Dig directly into raw data wherever it lives - EDC, exports, source documents - to get to the bottom of what it's saying.
  • Build and refine eCRFs and edit checks that catch bad data at entry (Castor today; we're building our own EDC - you'll help shape the system that makes the truth easy to see).
  • Set the standard for "clean" with our Philippines-based data team.
  • Sit between clinical, lab, regulatory, and engineering - your dataset is the thing all of them trust.

About RDI
At RDI Trials, we're building a different kind of CRO.
We are an IVD-focused contract research organization. Since 2008 we've run 300+ diagnostic trials for the largest test makers in the world.
This is not a traditional, process-heavy environment.
We are a small team that moves fast and expects people to take real ownership. There's no passing things along or waiting for direction. If something needs to get done, you step in and figure it out.
The pace is high. The expectations are high. But for the right person, it's a place where you can learn quickly and have real impact.
Requirements
  • 3+ years clinical data management in a regulated environment (IVD/diagnostics a strong plus).
  • An investigative instinct - you chase anomalies to root cause and aren't satisfied until you know why, not just what.
  • Hands-on EDC experience (Castor, Cloudbyz, REDCap, Medidata, or similar) and comfort working directly with raw data - we care that you get to the bottom of it, not which tool you reach for.
  • Command of the integrity discipline: SDV, query management, reconciliation, database lock, ALCOA+, Part 11.
  • Enough biostatistical literacy to tell real signal from artifact (concordance, outliers, method comparison) - without torturing the data to fit a conclusion.
  • The spine to tell the true story even when it's not the one people want to hear.
  • Bonus: FDA submission exposure (510(k), CLIA waiver); GCP/ICH familiarity.

What we're not looking for
  • Someone who reports the number without asking whether it's real.
  • A "storyteller" who starts with the conclusion and back-fills the data to match.
  • Extract, export, move on.

Benefits
  • Health Care Plan (Medical, Dental & Vision)
  • Retirement Plan (401k, IRA)
  • Life Insurance (Basic, Voluntary & AD&D)
  • Paid Time Off (Vacation, Sick & Public Holidays)

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