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Director Of Clinical Informatics Jobs in Santa Rosa, CA

BioTalent

Director Clinical Affairs

Santa Rosa, CA · On-site

$164K - $216K/yr

Director of Clinical Affairs We're seeking a Director of Clinical Affairs to own end-to-end execution of regulatory-driven clinical studies for a growing medical device company. This is a hands-on ...

BioTalent

Director Clinical Affairs

Sonoma, CA · On-site

$168K - $221K/yr

Director of Clinical Affairs We're seeking a Director of Clinical Affairs to own end-to-end execution of regulatory-driven clinical studies for a growing medical device company. This is a hands-on ...

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Director Of Clinical Informatics information

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How much do director of clinical informatics jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for director of clinical informatics in Santa Rosa, CA is $75.81, according to ZipRecruiter salary data. Most workers in this role earn between $57.31 and $94.86 per hour, depending on experience, location, and employer.

What is a director of clinical informatics?

A Director of Clinical Informatics is a healthcare professional responsible for overseeing the integration and management of clinical information systems within a healthcare organization. They ensure that electronic health records (EHRs) and other health IT systems are used effectively to improve patient care, streamline workflows, and maintain regulatory compliance. This role often involves collaborating with clinical staff, IT teams, and administrators to optimize data usage and support evidence-based clinical decisions.

How does a director of clinical informatics typically collaborate with clinical and IT teams to implement new health information systems?

A Director of Clinical Informatics serves as a critical bridge between clinical staff and IT professionals, ensuring that new health information systems align with both technological capabilities and clinical workflows. They lead multidisciplinary project teams, facilitate communication to translate clinical needs into technical requirements, and oversee training initiatives to promote user adoption. This role often involves mediating between differing priorities, troubleshooting integration challenges, and continuously gathering feedback to optimize system performance post-implementation.

What are the key skills and qualifications needed to thrive as a director of clinical informatics, and why are they important?

To thrive as a Director of Clinical Informatics, you need a robust background in healthcare, informatics, and leadership, often supported by advanced degrees (such as MSN or MPH) and certifications like CPHIMS or RN-BC in Informatics. Familiarity with electronic health record (EHR) systems, clinical decision support tools, data analytics platforms, and project management software is crucial. Exceptional communication, strategic thinking, and change management skills help drive cross-functional collaboration and facilitate technology adoption. These competencies are critical for aligning clinical workflows with technological advancements to improve patient outcomes and organizational efficiency.

What is the difference between Director Of Clinical Informatics vs Clinical Informatics Specialist?

AspectDirector Of Clinical InformaticsClinical Informatics Specialist
ResponsibilitiesOversees clinical informatics strategies, manages teams, and aligns technology with healthcare goals.Implements clinical informatics systems, provides user support, and assists in data analysis.
Required CredentialsTypically requires a master's degree in health informatics or related field, and relevant certifications.Often requires a bachelor's or master's degree in health informatics or related area, with certifications preferred.
Work EnvironmentHealthcare organizations, hospitals, or health systems, often in leadership roles.Clinical settings, hospitals, or clinics, focusing on system implementation and support.

The main difference is that the Director Of Clinical Informatics holds a leadership role overseeing strategies and teams, while the Clinical Informatics Specialist focuses on system implementation and support at a more operational level.

What job categories do people searching Director Of Clinical Informatics jobs in Santa Rosa, CA look for?

The top searched job categories for Director Of Clinical Informatics jobs in Santa Rosa, CA are:

What cities near Santa Rosa, CA are hiring for Director Of Clinical Informatics jobs?

Cities near Santa Rosa, CA with the most Director Of Clinical Informatics job openings:

Director Of Clinical Informatics jobs near you

Director Clinical Affairs

BioTalent

Santa Rosa, CA • On-site

$164K - $216K/yr

Other

Posted 17 days ago

Job description

Director of Clinical Affairs

We're seeking a Director of Clinical Affairs to own end-to-end execution of regulatory-driven clinical studies for a growing medical device company. This is a hands-on, operationally intense role for someone who has taken devices or SaMD from earliest-stage concept all the way through trial completion and into post-market surveillance — not just a single phase of the lifecycle.

What You'll Do

  • Own the full device/SaMD clinical lifecycle — from early-stage study design through trial execution, final study report, and post-market surveillance
  • Develop study design from scratch in close collaboration with internal management, regulatory advisors, reimbursement specialists, and KOL advisory committees
  • Lead clinical study execution — feasibility, site selection, activation, enrollment, monitoring, and close-out
  • Write and manage IRB/Ethics submissions, informed consent forms, and study essential documents
  • Select, qualify, and oversee third-party clinical sites and investigators as primary point of contact
  • Manage clinical data operations — eCRF design, data review, query resolution, vendor coordination
  • Develop study timelines, budgets, and risk mitigation plans, reporting clearly to leadership
  • Ensure compliance with FDA regulations (21 CFR Parts 11, 50, 56, 812, 820), ICH-GCP, ISO 14155, and SaMD guidance
  • Manage CRO and clinical vendor relationships, including contract negotiation and performance oversight
  • Collaborate cross-functionally with regulatory, product, engineering, and legal teams
  • Support RA/QA peers on FDA interactions, pre-subs, and 510(k) submissions
  • Build and scale the clinical operations function — SOPs, templates, and tracking systems
  • Maintain post-market surveillance activities, including adverse event monitoring and reporting


What You Bring

  • Minimum B.S. Degree with 10+ years hands-on clinical operations experience (5+ in leadership) running trials for FDA-regulated medical devices, SaMD/digital health, or combination products
  • Demonstrated experience owning a device or SaMD through the complete lifecycle — from initial concept and study design through trial completion and post-market surveillance
  • Track record of building study designs from scratch alongside key internal and external stakeholders
  • Experience with biosensing devices, consumer health tech, or wellness platforms pursuing clinical validation
  • Familiarity with RWE study designs and decentralized/hybrid trial models
  • Startup or scale-up experience building processes from scratch
  • Experience supporting breakthrough device designations or pre-sub meetings
  • Experience launching studies across multiple regions/countries, with direct exposure to varying regulatory bodies and government requirements
  • Track record of trials leading to FDA clearances/approvals or labeling expansions
  • Experience managing third-party clinical sites end-to-end (selection through close-out)
  • Proven ability authoring IRB/Ethics submissions, ICFs, and clinical protocols
  • 7+ years cross-functional program management across clinical, engineering, and regulatory
  • Strong clinical data management knowledge (eCRF, data cleaning, query management, database lock)
  • Fluency in FDA device regulations (IDE, De Novo, 510(k)), ICH-GCP, ISO 14155, and SaMD guidance
  • Experience with study budgeting, vendor management, and CRO oversight
  • KOL relationship-building experience

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