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Director Medical Informatics Jobs in California (NOW HIRING)

Sutter Health

Director, Clinical Science

Livermore, CA · On-site

$209K - $334K/yr

This position will function as director in charge of all required clinical science, new test ... Understanding of medical informatics and information systems as they affect laboratory clinical ...

Sutter Health

Director, Clinical Science

Livermore, CA · Hybrid

$209K - $334K/yr

This position will function as director in charge of all required clinical science, new test ... Understanding of medical informatics and information systems as they affect laboratory clinical ...

Eisenhower

Informaticist-Clinical

Rancho Mirage, CA

$39.04 - $59.31/hr

Clinical Informatics Job Objective: Supports the Medical Staff and Acute Care Services to enable ... Clinical Informatics Director Supervises: N/A Ages of Patients: N/A Blood Borne Pathogens: Minimal ...

PIH Health

Senior Health Informatics Analyst

Whittier, CA · On-site

$90K - $114K/yr

... medical (physician) group, home healthcare services and hospice care, as well as heart, cancer ... Four (4) years of direct experience using technical and analytical skills on the extraction ...

PIH Health

Senior Health Informatics Analyst

Whittier, CA · On-site

$76K - $126K/yr

... medical (physician) group, home healthcare services and hospice care, as well as heart, cancer ... Four (4) years of direct experience using technical and analytical skills on the extraction ...

Madera County, CA

Health Informatics Analyst II

Madera, CA · On-site

$76K - $93K/yr

Exercises no direct supervision over staff. Examples of Duties The job functions listed below are ... Gathers, compiles, and analyzes medical billing and statistical data and reviews encounters for ...

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Director Medical Informatics information

What are the key skills and qualifications needed to thrive as a director medical informatics?

To excel as a Director of Medical Informatics, you need a robust background in healthcare, clinical workflows, and health information management, often supported by an advanced degree in health informatics or related fields. Familiarity with electronic health record (EHR) systems, data analytics tools, and relevant certifications like CPHIMS is typically required. Strong leadership, project management, and communication skills help bridge the gap between clinical staff, IT teams, and executive leadership. These competencies are crucial for driving effective technology adoption, ensuring regulatory compliance, and optimizing patient care through data-driven decision-making.

What are the main challenges a director medical informatics faces when integrating new health IT systems across departments?

A Director of Medical Informatics often encounters challenges such as aligning the diverse needs of clinical, administrative, and IT teams when implementing new health IT systems. Ensuring data interoperability, maintaining regulatory compliance (such as HIPAA), and driving user adoption among staff are common hurdles. Effective communication and cross-departmental collaboration are crucial, as this role often serves as a bridge between technical teams and healthcare providers. Staying updated on emerging technologies and managing change management processes are also key aspects of the job.

What is a director medical informatics?

A Director of Medical Informatics is a senior leader responsible for overseeing the integration of information technology and data management into healthcare systems. They work to improve patient care, clinical workflows, and data accuracy by implementing and optimizing electronic health records (EHRs) and other health IT solutions. This role often serves as a bridge between clinical staff and IT professionals, ensuring that technology meets the needs of both. Directors of Medical Informatics also help develop policies, train staff, and ensure compliance with healthcare regulations. Their efforts support better decision-making and enhanced healthcare outcomes.

What are the most commonly searched types of Medical Informatics jobs in California?

The most popular types of Medical Informatics jobs in California are:

What are popular job titles related to Director Medical Informatics jobs in California?

For Director Medical Informatics jobs in California, the most frequently searched job titles are:

What job categories do people searching Director Medical Informatics jobs in California look for?

The top searched job categories for Director Medical Informatics jobs in California are:

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Cities in California with the most Director Medical Informatics job openings:

Director Medical Informatics jobs near you
Infographic showing various Director Medical Informatics job openings in California as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, 2% Temporary, and 5% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution.

Associate Director, Clinical Data Systems and Informatics

ClearNote Health

San Diego, CA • On-site

$155K - $190K/yr

Full-time

Re-posted 14 days ago

Job description

Job Title: Associate Director, Clinical Data Systems and Informatics
Location: San Mateo, CA; San Diego, CA
ClearNote Health is an early cancer detection company focused on the development and commercialization of non-invasive epigenomic tests to detect cancer through a standard blood draw, earlier than existing methods and when the disease is still treatable. Leveraging its novel liquid biopsy technology, ClearNote Health is initially focused on high-mortality cancers with the greatest need for early detection, starting with pancreatic and ovarian cancers.
Position Summary:
The Associate Director, Clinical Data Systems and Informatics will contribute to the development of our diagnostic tests through management of clinical data flow into our data warehouse and reporting on that data. This role will be instrumental to the success of our research efforts and our clinical trials with the management and organization clinical data. The data from the systems overseen will be integrated into our discovery and clinical research efforts, enabling precise, rigorous scientific decisions leading to the development of screening tests that meet our team's high standards.
Key Responsibilities:
  • Coordinate with clinical operations personnel to ensure data from Electronic Data Capture (EDC) systems is delivered into our Data Warehouse (DWH)
  • Author and maintain data management plan (DMP) for clinical studies, ensuring alignment with study requirements and ICH E6 (R2) GCP standards
  • Oversee the design, build, and validation of electronic case report forms (eCRFs), including edit check programming and UAT execution.
  • Manage data flow from site to EDC, ensuring timely resolution of queries and database integrity.
  • Develop and maintain data validation plans, including programmatic and manual edit checks to support ALCOA+ data quality principles
  • Lead the creation of data review listings and metrics reports to support ongoing data cleaning and study oversight
  • Coordinate with CRO or external CDM vendors on data management deliverables, timelines, and quality standards
  • Support database lock activities including final data reconciliation, discrepancy resolution, and lock documentation
  • Maintain TMF-relevant CDM documentation in accordance with regulatory inspection readiness standards
  • Coordinate with clinical operations personnel to ensure data from non-EDC sources (e.g. ad hoc spreadsheets) is delivered into our DWH
  • Transform clinical data in the DWH into forms suitable for use by the entire research and development team
  • Own the accuracy and integrity of all clinical data in the DWH
  • Serve as an SME on DWH clinical data for the research and development team
  • Coordinate with our Regulatory/QA team to ensure clinical data flow and the DWH are compliant with procedural and regulatory requirements
  • Define methods and metrics for assessing data quality; monitor and maintain data quality
  • Integrate clinical data with other corporate data
  • Provide project status updates to cross-functional team members.
  • Provide technical guidance and training in the use of clinical data in the DWH
Qualifications:
  • 7+ years of clinical data management experience
  • Hands-on, technically adept
  • Experience working in hybrid CDM role spanning both hands-on study execution and oversight
  • Software engineering expertise
  • Expert understanding of database and DWH concepts
  • Experience with EDC platforms including eCRF design, edit check authorizing, and study administration
  • Ability to author CDM-critical documents including DMPs, CRF completion guidelines, data validation plan, and SOPs
  • Working knowledge of clinical data standards (CDASH/CDISC preferred)
  • Familiarity with query management workflows and data lock/freeze procedures
  • Deep expertise in SQL
  • DBT experience required
  • Python experience preferred
  • Strong writing skills and experience documenting your work
  • In-depth clinical database build knowledge. Medrio experience preferred.
  • Working knowledge of Good Clinical Practices, clinical research, clinical trial process and related regulatory requirements
  • Familiar with cancer related medical classifications and ontologies such as ICD-10
  • Strong communication skills
The anticipated salary range for this position is $155,000 - $190,000. The actual salary will be dependent on various factors that may include experience level, knowledge, skills and abilities.
Come join us in addressing large healthcare needs through precision epigenomic medicine!
ClearNote Health is an exciting life science company that is reinventing non-invasive molecular diagnostic testing using next generation epigenomic technologies. We are passionate and dedicated to discovering and developing medicines that will make a significant difference in cancer and other epigenomic-driven diseases. Our technologies provide novel insight and quantitation of human health and disease, with our focus on precision medicine applications improving both clinical and health system outcomes. Our company was founded based on pioneering work in the Stanford laboratory of Stephen Quake, with advisors from Stanford and UCSF.
We look for extraordinary lifelong learners with a passion and growth mindset for these areas, and for combining biological ingenuity with AI and data analysis. Led by a team with decades of experience bringing products from concept to market, we are an equal opportunity employer and value diversity at our company.
We provide generous benefits to all employees including stock options. We are building a world-class company, based in San Diego and San Mateo.
Our commitment to Diversity, Equity, Inclusion, and Belonging:
We celebrate diversity in perspectives and backgrounds, and this is reflected in our innovation, our mission, and values. Our differences make us unique, help us innovate, and allow us to persevere. We strive to achieve representation and inclusion and redefine the possible in patients living longer lives.

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