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Edc Programmer Jobs in California (NOW HIRING)

Lyles Construction Group

I&C Engineer III

Sacramento, CA · On-site

$120K - $132K/yr

Prepare and review Electrical Distribution and Controls (EDC) submittal packages, including marked-up specifications, deviation lists, engineering drawings, and bills of material. * Select process ...

Lyles Construction Group

I&C Engineer II

Sacramento, CA · On-site

$99K - $109K/yr

Prepare and review Electrical Distribution and Controls (EDC) submittal packages, including marked-up specifications, deviation lists, engineering drawings, and bills of material. * Develop Field ...

Actalent

Clinical Research Coordinator

Palo Alto, CA

$37 - $45/hr

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 ...

Actalent

Clinical Research Coordinator

Palo Alto, CA

$37 - $45/hr

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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All JobsEdc Programmer JobsEdc Programmer Jobs in California

Edc Programmer information

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$11

$39

$67

How much do edc programmer jobs pay per hour?

As of Aug 6, 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 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 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.

Do edc programmers get paid well?

EDC programmers typically earn competitive salaries that reflect their specialized skills in embedded systems, programming languages, and hardware integration. Compensation varies based on experience, location, and industry, with many earning above average wages for technical roles. Certifications and proficiency with tools like C, C++, or assembly can also influence pay levels.

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 most commonly searched types of Edc Programmer jobs in California? The most popular types of Edc Programmer jobs in California are:
What are popular job titles related to Edc Programmer jobs in California? For Edc Programmer jobs in California, the most frequently searched job titles are:
What job categories do people searching Edc Programmer jobs in California look for? The top searched job categories for 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:
Edc Programmer jobs near you
Infographic showing various Edc Programmer job openings in California as of August 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.

Sr. Director, Clinical Data Management

ALX Oncology Inc.

South San Francisco, CA • On-site

$240K/yr

Full-time

Retirement

Posted 5 days ago

Job description

Reporting to the VP, Biometrics, the Sr. Director, Clinical Data Management provides strategic and operational leadership for the Clinical Data Management function across ALX Oncology's development portfolio. As the senior data management leader in a lean biotechnology environment, this individual is responsible for establishing a scalable, fit-for-purpose function that delivers high-quality clinical trial data to support development milestones, regulatory submissions, and future portfolio growth. This role requires a leader who can think strategically while remaining hands-on, building effective partnerships and driving operational excellence in a dynamic, resource-focused organization.
Preference will be given to candidates who can regularly work onsite Mondays and Tuesdays as part of the company's hybrid work model.
Key Responsibilities include:
  • Lead the Clinical Data Management function by developing and executing strategies, processes, and operational plans that support ALX Oncology's clinical development portfolio and align with the objectives of the Biometrics organization.
  • Oversee Clinical Data Management activities across the development portfolio, including review and approval of key deliverables such as database design, eCRFs, edit checks, data review plans, and database lock activities.
  • Lead data review, issue management, and milestone readiness to support interim analyses, database locks, and key development milestones.
  • Serve as the primary escalation point for data management issues affecting study quality, timelines, or regulatory readiness.
  • Oversee EDC and related clinical data systems, including implementation, configuration, and vendor management.
  • Lead the selection, oversight, and performance management of CROs and specialty vendors, establishing governance, performance metrics, and communication processes to ensure high-quality execution and accountability.
  • Manage vendor budgets and identify cost-effective solutions without compromising quality or compliance.
  • Drive continuous improvement initiatives that enhance data quality, operational efficiency, and study execution.
  • Partner with Clinical Operations, Biostatistics, Statistical Programming, Clinical Science, Medical, Safety, Regulatory, and Quality to support successful study execution.
  • Provide data management expertise during protocol development, advising on data collection strategy, endpoint feasibility, and study design.
  • Ensure clinical data are inspection-ready and support regulatory submissions, audits, safety reviews, and due diligence activities.

  • Contribute to a culture that reflects ALX's values by acting with integrity, accountability, transparency, and respect. Build strong, collaborative relationships through active engagement with colleagues, including regular onsite participation consistent with the company's hybrid work model.

Preferred Qualifications include:
  • Bachelor's degree in Life Sciences, Statistics, Computer Science, or a related scientific discipline, or an equivalent combination of education and directly relevant work experience. Advanced degree (MS, MPH, PhD) is a plus.
  • Approximately 12+ years of progressive Clinical Data Management experience within biotechnology, pharmaceutical, or CRO environments, including Phase I-III clinical studies, with demonstrated success leading outsourced Clinical Data Management activities, partnering across functions, and delivering high-quality clinical trial data. Experience supporting regulatory submissions is preferred. Oncology and/or immuno-oncology experience is strongly preferred.
  • Strong knowledge of Clinical Data Management principles, GCP, applicable regulatory requirements, CDISC standards, and industry best practices, with demonstrated expertise in database design, data cleaning, medical coding, external data reconciliation, data review, database lock, and other core Clinical Data Management processes. Experience with leading EDC platforms such as Medidata Rave, Veeva EDC, Oracle Clinical, or equivalent systems.
  • Demonstrated ability to effectively manage CROs, vendors, budgets, and outsourced Clinical Data Management activities.
  • Strategic, collaborative leader with excellent communication, organizational, and relationship-building skills, capable of influencing cross-functional teams and external partners.
  • Demonstrated ability to prioritize competing demands, solve complex problems, build scalable processes, and adapt to evolving business priorities while contributing beyond functional boundaries in a fast-paced, resource-constrained environment.

Compensation
The salary range for this position at our South San Francisco, CA corporate office is $240,000 - $280,000. Additional factors such as academic credentials and relevant experience will influence the actual salary offered. In addition to a competitive market-based salary, ALX Oncology offers the opportunity to participate in stock programs, a performance-based bonus, and a comprehensive benefits package including 401K. Additional information can be found here: https://alxoncology.com/careers/
About ALX Oncology
ALX Oncology (Nasdaq: ALXO) is a clinical-stage biotechnology company advancing a pipeline of novel therapies designed to treat cancer and extend patients' lives. ALX Oncology's lead therapeutic candidate, evorpacept, has demonstrated potential to serve as a cornerstone therapy upon which the future of immuno-oncology can be built. Evorpacept is currently being evaluated across multiple ongoing clinical trials in a wide range of cancer indications. ALX Oncology's second pipeline candidate, ALX2004, is a novel EGFR-targeted antibody-drug conjugate with a differentiated mechanism of action. A Phase 1, dose-escalation trial of ALX2004 is ongoing in patients with EGFR-expressing solid tumors. More information is available at www.alxoncology.com and on LinkedIn @ALX Oncology.
Information for Recruitment Agencies
Please note that ALX Oncology does not accept unsolicited resumes or candidate information from recruitment agencies, including blinded or anonymized resumes, and will not be responsible for any fees associated with unsolicited submissions. Do not contact hiring managers or other ALX Oncology employees directly. Recruiting activities are managed through our Human Resources team.

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