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Director Clinical Coding Jobs in California (NOW HIRING)

UCLA Outpatient Clinics

Coding Supervisor

Los Angeles, CA · On-site

$67K - $134K/yr

Description Under the direction of the Physician Billing Office (PBO) Coding Director, the Coding ... Serve as a resource for coding staff, physicians, and clinical departments regarding coding ...

UCLA Health

Coding Supervisor

Los Angeles, CA · On-site

$67K - $134K/yr

... Coding Director, the Coding Department Supervisor oversees the daily operations of a team of ... Serve as a resource for coding staff, physicians, and clinical departments regarding coding ...

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All JobsClinical Coding JobsDirector Clinical Coding JobsDirector Clinical Coding Jobs in California

Director Clinical Coding information

What is the difference between Director Clinical Coding vs Clinical Coding Manager?

AspectDirector Clinical CodingClinical Coding Manager
CredentialsCertifications in coding and management, relevant degreesCertifications in coding, management experience
Work EnvironmentStrategic leadership, overseeing coding departmentsOperational management, supervising coding teams
Industry UsageHealthcare organizations, hospitals, health systemsHospitals, clinics, healthcare providers
Search IntentUnderstanding leadership roles in codingManaging coding teams and processes

The main difference between a Director Clinical Coding and a Clinical Coding Manager lies in their scope of responsibilities. The Director typically focuses on strategic oversight and departmental leadership, while the Manager handles day-to-day operations and team supervision. Both roles require relevant certifications and experience in clinical coding, but the Director's role is more senior and strategic.

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The most popular types of Clinical Coding jobs in California are:

What are popular job titles related to Director Clinical Coding jobs in California?

For Director Clinical Coding jobs in California, the most frequently searched job titles are:

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The top searched job categories for Director Clinical Coding jobs in California are:

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Director Clinical Coding jobs near you
Infographic showing various Director Clinical Coding job openings in California as of September 2026, with employment types broken down into 3% As Needed, 74% Full Time, 16% Part Time, and 7% Contract. Highlights an 86% Physical, 1% Hybrid, and 13% Remote job distribution.

Sr. Director, Clinical Data Management

South San Francisco, CA • On-site

ALX Oncology Inc.
Biotechnology Research and Development • 11 - 50 employees
Learn more about ALX Oncology Inc.external

Full-time

Retirement

Re-posted 12 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.

Not sure if you are qualified for this position? We know that skills and experience can show up in different ways and we welcome resumes from a broad range of applicants. You are encouraged to apply even if you do not meet each of the preferred qualifications.
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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