ZipRecruiter

Log In

1

Study Monitor Jobs in California (NOW HIRING)

Cordis

Clinical Study Manager

Irvine, CA · On-site +1

$114K - $165K/yr

Monitor enrollment, data quality, and protocol compliance; implement mitigation strategies as needed. * Conduct cross-functional team meetings and maintain effective communication among study ...

Cordis

Clinical Study Manager

Irvine, CA · On-site +1

$114K - $165K/yr

Monitor enrollment, data quality, and protocol compliance; implement mitigation strategies as needed. * Conduct cross-functional team meetings and maintain effective communication among study ...

Stryker

Principal Clinical Study Manager

Fremont, CA · Remote

$153K - $255K/yr

Monitor study performance through metrics and reporting, implementing corrective actions and maintaining clear communication with sites and stakeholders. * Support regulatory submissions (e.g., IDEs ...

Apple

Clinical Study Operations Associate

Cupertino, CA

$126K - $190K/yr

Monitor the quality and completeness of datasets returned from clinical studies in progress. Train external collaborators on study procedures and monitor their performance. Extended domestic travel ...

Apple

Clinical Study Operations Lead

Cupertino, CA

$147K - $220K/yr

Monitor the quality and completeness of datasets returned from clinical studies in progress. Train external collaborators on study procedures and monitor their performance. Extended domestic travel ...

next page

Showing results 1-20

All JobsStudy Monitor JobsStudy Monitor Jobs in California

Study Monitor information

What are the key skills and qualifications needed to thrive in the Study Monitor position, and why are they important?

To thrive as a Study Monitor, you need a strong understanding of clinical trial protocols, regulatory guidelines (such as GCP), and data integrity principles, typically supported by a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like ACRP or SOCRA are commonly expected. Excellent attention to detail, strong organizational skills, and effective communication are crucial soft skills. These competencies ensure high-quality study oversight, compliance with regulations, and smooth collaboration among clinical research teams.

What are some common challenges Study Monitors face during clinical trials?

Study Monitors often encounter challenges such as ensuring consistent protocol adherence across multiple sites, managing discrepancies in data, and navigating tight timelines for site visits and reporting. They must adapt quickly to evolving regulatory requirements and effectively communicate any issues or deviations to investigators and sponsors. Being proactive in identifying potential risks and fostering strong relationships with site staff can help minimize these challenges. As a result, successful Study Monitors need to be resourceful, detail-oriented, and skilled at balancing regulatory compliance with practical problem-solving in dynamic trial environments.

What is a Study Monitor job?

A Study Monitor, also known as a Clinical Research Associate (CRA), is responsible for overseeing clinical trials to ensure they comply with regulatory guidelines, study protocols, and ethical standards. They monitor site activities, review data accuracy, and ensure participant safety. Study Monitors work closely with investigators, site staff, and sponsors to ensure the integrity of trial results and adherence to Good Clinical Practice (GCP) guidelines.

What are popular job titles related to Study Monitor jobs in California? For Study Monitor jobs in California, the most frequently searched job titles are:
What job categories do people searching Study Monitor jobs in California look for? The top searched job categories for Study Monitor jobs in California are:
What cities in California are hiring for Study Monitor jobs? Cities in California with the most Study Monitor job openings:
Study Monitor jobs near you
Infographic showing various Study Monitor job openings in California as of June 2026, with employment types broken down into 1% As Needed, 80% Full Time, 16% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 94% Physical, 3% Hybrid, and 3% Remote job distribution.

Assistant Clinical Research Coordinator

Om Research LLC

Camarillo, CA • On-site

$16 - $25/hr

Full-time

Posted 4 days ago

Job description

The Assistant Clinical Research Coordinator comprises an integral part of the research team. Working under the PI, he/she is responsible for conducting the study in accordance with federal regulations. Some responsibilities of the Clinical Research Coordinator include:

1. Preparing for study initiation

2. Obtaining physician signatures

3. Recruiting subjects

4. Screening and scheduling subjects

5. Getting voluntary subject consent

6. Teaching subjects about protocol expectations for them

7. Performing study/protocol procedures in a detailed, accurate manner

8. Maintaining study files

9. Tracking subjects, avoiding lost-to-follow-up

10. Documenting an adverse event

11. Processing and shipping lab work

12. Maintaining communication and correspondence (by telephone, email, fax, etc.) with subjects, sponsor, monitor and other site study personnel

13. Completing case report forms (CRF's) for PI review and approval

14. Helping study monitors with CRA corrections

15. Maintaining study-specific supplies

16. Preparing for study closure and archiving

Knowledge of Spanish and / or Phlebotomy Training will be an added advantage.