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Edc Programmer Jobs in California (NOW HIRING)

Exelixis

Senior AI Data Scientist I

Alameda, CA

Leveraging statistical programming (R, Python, SQL) and machine-learning techniques, this role ... Execute data cleaning, transformation, and standardization tasks across clinical datasets from EDC ...

Exelixis

Senior AI Data Scientist I

Alameda, CA · On-site

Leveraging statistical programming (R, Python, SQL) and machine-learning techniques, this role ... Execute data cleaning, transformation, and standardization tasks across clinical datasets from EDC ...

Exelixis

Senior AI Data Scientist I

Alameda, CA · On-site

Leveraging statistical programming (R, Python, SQL) and machine-learning techniques, this role ... Execute data cleaning, transformation, and standardization tasks across clinical datasets from EDC ...

Alphatec Spine

Clinical Scientist II

Carlsbad, CA

$125K - $140K/yr

Prepare clear, complete and accurate technical engineering documentation. * Contribute to the ... Familiarity with electronic data capture systems (EDC, EMR), data analysis, and data visualization.

Alphatec Spine

Clinical Scientist II

Carlsbad, CA · On-site

$125K - $140K/yr

Prepare clear, complete and accurate technical engineering documentation. * Contribute to the ... Familiarity with electronic data capture systems (EDC, EMR), data analysis, and data visualization.

Alphatec Spine

Clinical Scientist II

Carlsbad, CA · On-site

$125K - $140K/yr

Prepare clear, complete and accurate technical engineering documentation. * Contribute to the ... Familiarity with electronic data capture systems (EDC, EMR), data analysis, and data visualization.

Xencor

Director, Clinical Data Management

San Diego, CA · On-site

More than 20 XmAb drug candidates engineered with our technology are in clinical development, and ... Provides training of the CRF completion guidelines, EDC system at Investigators' meeting and to ...

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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 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 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.

Lead Clinical Data Manager

CooperCompanies

San Ramon, CA • On-site

Full-time

Re-posted 18 days ago

Job description


At CooperVision, a division of CooperCompanies, we're driven by a unifying purpose to help people to experience life's beautiful moments. We are connected through our shared values - dedicated, innovative, friendly, partners, and do the right thing. As a leading global manufacturer of contact lenses, we are committed to helping improve the way people see each day. Through our diverse lens portfolio, we tackle the toughest vision challenges - including astigmatism, presbyopia, and childhood myopia. We offer the most complete collection of spherical, toric, and multifocal products available, enabling us to fit 99% of all contact wearers. Learn more at www.coopervision.com.
  • This role is not eligible for employer-sponsored work authorization now or in the future. Applicants must be authorized to work in the United States on a permanent and ongoing basis without the need for future sponsorship (i.e., H1B, STEM OPT extensions, TN, etc.)
  • This position requires full-time onsite work (5 days per week) in San Ramon, CA and is not eligible for relocation assistance.

Job Summary:
Leads all aspects of clinical data management activities from study initiation through database lock and study closeout. Develops, optimizes and controls data management system, including external clinical research centers in compliance with medical device regulations. Oversees and ensure that all CooperVision sponsored clinical trial data are accurate, complete, and compliant.
  • This role is not eligible for employer-sponsored work authorization now or in the future. Applicants must be authorized to work in the United States on a permanent and ongoing basis without the need for future sponsorship (i.e., H1B, STEM OPT extensions, TN, etc.)
  • This position requires full-time onsite work (5 days per week) in our San Ramon, CA. office and is not eligible for relocation assistance.

Responsibilities
  • Generate, contribute, and/or review key study documentation such as data management plans, case report forms (CRFs), database specifications, test plans for user acceptance testing (UAT), and data transfer specification and agreements
  • Lead electronic case report form (eCRF) developments and facilitate cross-functional reviews of eCRF content
  • Support the design, development, and validation of clinical trial databases and eCRFs, including edit checks within the Electronic Data Capture (EDC) system
  • Perform training on the EDC system, dataflow, and quality control (QC) processes to personnel as appropriate
  • Perform and/or oversee data cleaning, issue queries, query resolution, and delivery of high-quality datasets to support trial milestones and regulatory submissions; assist Clinical Operations, Biostatistics, Statistical Programming, Investigational sites, and/or Clinical Research Organization with resolving queries
  • Perform third party non-Case Report Form data management activities
  • Ensure delivery of datasets, annotated CRFs, and related materials in the appropriate formats
  • Participate in the preparation, review, and validation of submission-ready datasets for regulatory filings (e.g., FDA, EU MDR, PMDA, NMPA).
  • Lead efforts in developing and maintaining standard database validation checks for common modules as well as for indication or research objective specific modules
  • Ensure that documentation and data records, including archiving, meet regulatory and inspection standards
  • Ensure compliance with industry standards and regulations (ISO, FDA, EU MDR) and assist in audit and inspection readiness
  • Champion and assist the effective utilization of AI tools to enable automation, continuous process improvements, technology modernization, and efficiency initiatives.
  • Serve as the main liaison for vendors or partners handling data deliverables, clarifying expectations and maintaining streamlined communication between internal and external teams
  • Develop and/or modify standard operating procedures (SOPs) for clinical data management to comply with industry standards and regulations
  • Establish and manage data quality standards, ensuring adherence to internal procedures and external guidelines
  • Perform importing and reconciling external datasets, maintaining consistency across all study databases
  • Track and communicate progress metrics, risks, and outcomes to senior management
  • Coordinate closely with functional leads in Clinical Research, Clinical Operations, Biostatistics, Safety, and/or Regulatory Affairs to ensure seamless data flow and reporting

Travel Requirements:
Minimal travel (5%) required, occasionally to research centers to establish or improve data management procedures.
Qualifications
Knowledge, Skills and Abilities:
  • Bachelor's degree in life science, computer science or closely related discipline plus minimum of 8 years of experience in Clinical Data Management, or
  • Master of Science in life science, computer science or closely related discipline plus minimum of 5 years of experience in Clinical Data Management
  • Highly dependable, good time management and multitasking skillsets
  • Proficiency with common electronic data capture (EDC) and clinical data management platforms, and clinical data systems (e.g., REDCap, Medrio, Medidata RAVE, Veeva).
  • Expertise in database design, validation, and oversight of external data integration.
  • Expert in the use of SQL to query datasets.
  • Passion for exploring and adopting emerging technologies, including AI-enabled tools, to support innovation, operational excellence, and business transformation
  • Strong problem-solving ability to navigate complex unforeseen situations
  • Strong leadership skillsets to guide and mentor within and cross-functional team members
  • Strong on written and verbal communications
  • Experience with integrating data from external vendors or systems.
  • Familiarity with statistical or visualization tools such as SAS or R is preferred.
  • Ability to read and understand highly technical material.

Work Environment:
  • On-site 5 days a week in-office required
  • Normal office environment and ophthalmic clinical exam room
  • Sedentary to light physical effort necessary to perform the job.
  • Extensive contact with employees and external researchers
  • Extensive computer and keyboarding

For U.S. locations that require disclosure of compensation, the starting base pay for this role is between $164,819.00 and $219,758.00. per year and may include cost of living adjustments. The actual base pay includes many factors and is subject to change and modification in the future. This position may also be eligible for other types of compensation and benefits.
We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender, gender identity or expression, or veteran status. We are proud to be an equal opportunity workplace.
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