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Associate Clinical Manager Jobs in California (NOW HIRING)

Individual Contributor (IC) Supervisor/Manager Title: Director, Clinical Affairs Job Location & Environment: Irvine, CA, Corporate Office Summary: The Clinical Research Associate will report to the ...

Clinical Manager

Sacramento, CA · On-site

$41.72 - $43.80/hr

... Associate (within 500 hours of licensure & BBS registered) * $41.72 hourly Licensed (LMFT, LCSW, LPCC, etc.) * $43.80 hourly About the Position: The Clinical Manager is responsible for the day to day ...

Depending on scope and phase of project, may support multiple projects. • Provides project management expertise throughout the development and implementation of clinical studies. Interacts with ...

Showing results 41-60

Associate Clinical Manager information

How does an associate clinical manager typically collaborate with cross-functional teams within a healthcare setting?

Associate Clinical Managers often serve as a bridge between clinical staff, administrative teams, and other departments such as quality assurance and human resources. They facilitate effective communication to ensure patient care objectives are met, coordinate schedules or resources, and help implement new protocols or processes. Regular meetings, interdisciplinary rounds, and collaborative problem-solving are common, making strong interpersonal and organizational skills essential for success in this role.

What is the difference between Associate Clinical Manager vs Clinical Supervisor?

AspectAssociate Clinical ManagerClinical Supervisor
Required CredentialsBachelor's degree in healthcare or related field; some roles may require certificationBachelor's or master's degree in healthcare; relevant licensure or certification often preferred
Work EnvironmentHealthcare facilities, clinics, hospitals, supporting clinical teamsHealthcare settings, overseeing clinical staff and patient care
Employer & Industry UsageHospitals, clinics, healthcare organizations; common in healthcare managementHospitals, outpatient clinics, healthcare organizations; focuses on staff supervision

The Associate Clinical Manager and Clinical Supervisor roles both involve supporting clinical teams in healthcare settings. The Associate Clinical Manager often has broader administrative responsibilities and may be on a pathway to management, while the Clinical Supervisor primarily oversees daily clinical operations and staff. Both roles require relevant healthcare credentials and are integral to patient care quality and team coordination.

What are the key skills and qualifications needed to thrive as an associate clinical manager, and why are they important?

To thrive as an Associate Clinical Manager, you need a background in healthcare management, clinical expertise, and a relevant degree such as nursing or healthcare administration. Familiarity with clinical information systems, quality assurance protocols, and regulatory compliance tools is typically required. Leadership, problem-solving, and strong interpersonal communication distinguish top performers in this role. These skills ensure effective team management, regulatory adherence, and high standards of patient care in clinical settings.
What are the most commonly searched types of Clinical Manager jobs in California? The most popular types of Clinical Manager jobs in California are:
What are popular job titles related to Associate Clinical Manager jobs in California? For Associate Clinical Manager jobs in California, the most frequently searched job titles are:
What cities in California are hiring for Associate Clinical Manager jobs? Cities in California with the most Associate Clinical Manager job openings:
Infographic showing various Associate Clinical Manager job openings in California as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, 2% Temporary, and 1% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution.

Full-time

Re-posted 17 days ago


Job description

Job Title: Associate, Clinical Research  

Role Level: Individual Contributor (IC) 

Supervisor/Manager Title: Director, Clinical Affairs 

Job Location & Environment: Irvine, CA, Corporate Office

Job Description Summary: The Clinical Research Associate will report to the Director, Clinical Affairs, and will play a key role in proactively supporting the conduct of pre-market and or post-market clinical studies and ensure compliance with all regulatory requirements. The ideal candidate will have a thorough knowledge of Good Clinical Practices (GCP) and applicable regulations. 

Job Responsibilities: 

  • Support site management and interact with site coordinators, investigators, and field monitors in collecting data and resolving queries to meet the protocol requirements in a timely manner.
  • Ensure quality data management activities – i.e., data review, query generation and resolution. Generate status reports to clinical staff and management.
  • Maintain Trial Master Files and trackers for clinical trials.
  • Manage trial-related regulatory documents and provide follow-up action listings to ensure that all clinical documentation required by regulations and JenaValve procedures is current.
  • Conduct periodic audits of internal files to ensure compliance per site Institutional Review Board (IRB) and/or Ethics Committee (EC) policy (i.e. IRB continuing review approval period and expiration dates). 
  • Provide clinical operational support during preparation for and conduct of all clinical audits and inspections.
  • Contribute to the development and implementation of departmental policies, standards, and process improvement initiatives. 
  • Partner with management to manage external vendors, including ongoing supplier qualification.
  • Assist field clinical monitors in preparation for site training and monitoring visits
  • Support monitoring of sites on an as-needed basis.

Required Education and Experience: 

  • At least 1 year of experience in clinical trial research is required (preferred in medical devices).
  • Advanced degree in a biological science / pharmacy/ nursing desired.

Skills and Abilities Required for This Job: 

  • Proficient in clinical trial management and electronic data capture systems to document and record information.
  • Excellent communication skills (written and verbal English) so as to be able to build effective relationships with trial center staff and colleagues.
  • Some knowledge of GCPs governing the conduct of clinical trials, Medical Device Directive 93/42/EEC, ISO14155 and ICH guidelines. 
  • Very organized and able to pay close attention to detail.
  • Team player with a willingness to help where needed and work with diverse people.

Physical Requirements

  • Ability to travel up to 20% time.