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Clinical Service Associate Jobs in California (NOW HIRING)

Patient Services Associate

Long Beach, CA · On-site

$18 - $22.50/hr

Patient Service Associate MEDNAX has grown from a single medical practice to a trusted health ... Ensure the clinical staff submits all outpatient billing sheets daily. * Maintains patient ...

Showing results 41-60

Clinical Service Associate information

What is the difference between Clinical Service Associate vs Clinical Research Coordinator?

AspectClinical Service AssociateClinical Research Coordinator
Required CredentialsHigh school diploma or equivalent; some roles may require certificationBachelor's degree in health sciences or related field; certification often preferred
Work EnvironmentHospitals, clinics, outpatient facilitiesResearch sites, hospitals, academic institutions
Employer & IndustryHealthcare providers, hospitals, clinicsResearch organizations, pharmaceutical companies, academic research centers
Common Search & ComparisonOften compared for roles supporting clinical operationsFocuses on managing clinical trials and research activities

The Clinical Service Associate primarily supports clinical operations within healthcare settings, focusing on patient care and administrative tasks. In contrast, the Clinical Research Coordinator manages clinical trials, ensuring compliance and data integrity. Both roles require strong organizational skills but differ in their focus on patient care versus research management.

What are the most commonly searched types of Clinical Service jobs in California?

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

Infographic showing various Clinical Service Associate job openings in California as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

Senior Staff Clinical Quality Associate (Onsite)

Stryker

Fremont, CA • On-site

$143K - $238K/yr

Full-time

Posted 14 days ago


Job description

Work Flexibility: Hybrid or Onsite
Stryker is hiring a Senior Staff Clinical Quality Associate for our Neurovascular division. This is an onsite role based in Fremont, CA or Salt Lake City, UT.
As the Senior Staff Clinical Quality Associate, you will focus on clinical quality, compliance governance, and regulatory readiness across global clinical research activities. You will provide oversight of quality systems, compliance programs, audits, inspections, and clinical processes to ensure clinical services, documentation, and operations align with applicable regulations and quality standards. You will work across functions to identify risks, strengthen controls, and support the continuous improvement of clinical quality programs.
This role provides quality and compliance oversight for clinical research activities, ensuring processes, documentation, systems, and vendor operations remain compliant, inspection-ready, and aligned with global regulatory and quality requirements.
What you will do
  • Manage clinical quality and compliance programs, establishing milestones, resource plans, and delivery timelines to support on-time execution
  • Identify, assess, and communicate compliance risks and control strategies to stakeholders across clinical, quality, and business functions
  • Lead internal and external audit and inspection activities, including preparation, execution, follow-up actions, and documentation management
  • Participate in regulatory inspections, including inspections of clinical studies conducted by regulatory authorities
  • Conduct vendor audits and inspections, maintain audit schedules, and monitor supplier compliance with quality requirements
  • Analyze process deviations, determine corrective actions, and update procedures to maintain compliance with applicable regulations and standards
  • Develop, maintain, and revise standard operating procedures, work instructions, and quality documentation
  • Deliver compliance training, provide guidance on clinical quality requirements, and support continuous improvement initiatives across the clinical organization

What you need
Required
  • Bachelor's degree
  • Minimum 7 years of experience in clinical quality, clinical research, quality assurance, compliance, or a related regulated healthcare or life sciences field
  • Minimum 5 years of experience supporting quality systems, regulatory compliance programs, audits, or inspections
  • Experience supporting clinical studies conducted within a regulated environment

Preferred
  • Experience in medical device, pharmaceutical, biotechnology, or clinical research industries
  • Experience participating in regulatory inspections and audit readiness activities
  • Experience developing and maintaining standard operating procedures and quality system documentation
  • Certified Quality Auditor (CQA), Regulatory Affairs Certification (RAC), or comparable quality or compliance certification

  • US5: $115,600 - $192,600 USD Annual
  • US30: $143,100 - $238,400 USD Annual

Travel Percentage: 30%
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.
Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information.