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Edc Programmer Jobs in California (NOW HIRING)

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 ...

Cooper Companies

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 ...

CYNET SYSTEMS

Clinical Data Manager

Sunnyvale, CA · On-site

$70 - $75/hr

Excellent hands on experience on SAS or R programming language for data review listings/tracker ... Understand CRF design and interpretation of protocol/CRF requirements to efficient EDC design.

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How much do edc programmer jobs pay per hour?

As of Jun 11, 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 industry, 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 Scientists and Cybersecurity Directors also command high compensation due to their expertise and demand for advanced skills and certifications.

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 job makes $10,000 a month without a degree?

An EDC programmer, or Electronic Data Capture programmer, can potentially earn $10,000 or more per month by developing and maintaining software for electronic data collection systems, often in healthcare or clinical research. Success in this role depends on experience, technical skills, and industry demand, with some professionals working freelance or in specialized consulting roles to achieve high earnings without a formal degree.

What qualifications do I need to be a coder?

To become an EDC programmer, a strong foundation in programming languages such as C, C++, or Python is essential, along with knowledge of embedded systems and hardware interfaces. A relevant degree in computer science, electrical engineering, or a related field is often preferred, and experience with development tools and debugging is valuable. Certifications in programming or embedded systems can also enhance job prospects.

What is an EDC programmer?

An EDC programmer is a professional who develops, tests, and maintains electronic data capture (EDC) systems used in clinical trials and research. They typically work with specialized software to ensure accurate data collection, often requiring knowledge of programming languages, database management, and regulatory standards. This role involves collaboration with clinical teams to optimize data workflows and ensure compliance.

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.

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Edc Programmer jobs near you
Sr. Director/Head of Data Management

Sr. Director/Head of Data Management

ALX Oncology Inc.

South San Francisco, CA

$240K - $280K/yr

Other

Posted 22 days ago

Job description

POSITION SUMMARY:
The Head of Data Management (Senior Director) is a key leadership role in a lean biotech company responsible for establishing and leading the Clinical Data Management function. This role will provide both strategic direction and hands-on execution to ensure high-quality clinical trial data that supports critical development milestones and future regulatory submissions.
In a small biotech environment, this leader must be comfortable operating with limited internal infrastructure, leveraging CRO and vendor partnerships, building pragmatic processes, and personally driving priorities when needed.
This position will report to the Head of BioMetrics.
PRIMARY RESPONSIBILITIES AND DUTIES:
  • Functional Leadership & Buildout
    • Serve as the functional lead for all Clinical Data Management activities across the development portfolio.
    • Provide input into Biometrics strategy and implement department initiatives
    • Build fit-for-purpose processes, standards, templates, and governance appropriate for a lean organization.
    • Develop a roadmap for scaling the function as programs advance.
    • Assess future hiring needs and organizational design as portfolio complexity increases.
  • Hands-On Study Execution
    • Interface with the project team to ensure that data management services are delivered in a consistent, high-quality manner.
    • Provide day-to-day oversight of outsourced data management activities for ongoing clinical studies.
    • Review and approve key deliverables including eCRFs, edit checks, data review plans, coding conventions, reconciliation plans, and database lock plans.
    • Act as internal escalation point for data issues impacting timelines, quality, or study milestones.
    • Lead data review, issue triage, and milestone readiness activities as needed.
  • CRO & Vendor Oversight
    • Lead management of CROs and specialty vendors providing EDC, eCOA/ePRO, coding, central labs, and related services.
    • Establish clear expectations, timelines, governance cadence, and performance metrics.
    • Ensure vendors remain aligned to company priorities and operate with urgency.
    • Manage budgets and identify cost-efficient solutions without compromising quality.
  • Cross-Functional Partnership
    • Work closely with Clinical Operations, Biostatistics, Statistical Programming, Clinical Science, Medical, Safety, Regulatory, and Quality team members.
    • Support protocol development by advising on data collection strategy, endpoint feasibility, and operational practicality.
    • Ensure data readiness for interim analyses, safety reviews, DSMB meetings, and topline readouts.
  • Systems & Process Optimization
    • Oversee EDC and related data systems selection, configuration strategy, and vendor management.
    • Implement streamlined processes that minimize burden while maintaining compliance.
    • Introduce dashboards and metrics to improve visibility to study progress and data quality.
  • Inspection Readiness & Corporate Support
    • Maintain documentation and processes that support diligence reviews, audits, and future inspections.
EDUCATION, EXPERIENCE, KNOWLEDGE, SKILLS AND ABILITIES:
  • Education
    • Bachelor's degree in Life Sciences, Statistics, Computer Science, or related discipline required.
    • Advanced degree preferred.
  • Experience
    • 10+ years of clinical data management experience in biotech, pharma, or CRO settings. At least 6 years of overall experience require acting as a project lead data manager
    • Prior leadership experience with responsibility for outsourced studies and vendor oversight.
    • Experience in small biotech or resource-focused environments strongly preferred.
    • Experience supporting Phase I/II/III studies required; Phase IV and submission experience a plus.
    • Experience in Oncology and/or Immuno-oncology trials preferred
  • Technical Expertise
    • Strong knowledge of EDC systems such as Medidata Rave, Veeva EDC, or Oracle platforms.
    • Solid understanding of data cleaning, coding, external data reconciliation, and database lock.
    • Familiarity with CDISC standards and submission expectations.
    • Strong vendor governance and budget management skills.
  • Leadership Style
    • Hands-on and comfortable working with focused internal teams.
    • Practical, solutions-oriented, and able to prioritize effectively.
    • Strong communicator who can influence across functions and with external partners.
SALARY RANGE: $240,000 - $280,000 DOE
PHYSICAL DEMANDS:
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed are representative of the knowledge, skill, and/or ability required.
  • Ability to communicate in written and oral forms.
  • Must be able to interact and communicate in written and oral forms with a diverse group of individuals on both technical and business topics.
  • The ability to sit, stand, kneel, stoop, walk, use hands to finger, handle, or feel, point, and reach with hands and arms.
  • Must be able to travel 25% of the time without restriction, domestically and/or internationally.
  • Must be able to use the telephone and communicate clearly with a host of external individuals, domestically and globally.
  • Ability to work at a computer for extensive periods of time.
  • Ability to work in a fast-paced working environment managing multiple tasks.

WORK ENVIRONMENT AND ENVIRONMENTAL CONDITIONS:
We offer flexible working models, competitive benefits, and an environment where you will have the opportunity for personal and professional growth.
ALX Oncology is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital and veteran status. Reasonable accommodation will be provided for qualified individuals with disabilities and for qualified disabled veterans in job application procedures, as required by applicable law.
The above description is intended to describe the general nature of the job and may include other duties as assumed or assigned; it is not intended to be all inclusive or limit the duties of the position.
ABOUT ALX ONCOLOGY
ALX Oncology is a clinical-stage and patient-focused immuno-oncology company developing therapies that block the CD47 myeloid checkpoint pathway. Our lead candidate, Evorpacept (ALX148), is a next generation CD47 blocking therapeutic that combines a high-affinity CD47 binding domain with an inactivated proprietary Fc domain. Our second pipeline candidate, ALX2004, is a novel EGFR-targeted antibody-drug conjugate with a differentiated mechanism of action and potential to be both first and best in class.
For more information about us, please visit www.alxoncology.com.

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