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Medical Device Cra Jobs in California (NOW HIRING)

Diality

Clinical Research Associate

Irvine, CA · Remote

$120K - $135K/yr

... the CRA position works closely with clinical sites, internal departments (e.g., medical affairs ... Previous experience in a medical device company or knowledge of device-specific regulatory pathways.

Diality Inc

Clinical Research Associate

Irvine, CA · On-site

... the CRA position works closely with clinical sites, internal departments (e.g., medical affairs ... Previous experience in a medical device company or knowledge of device-specific regulatory pathways.

Abbott

Clinical Research Associate II

Alameda, CA · On-site

$81K - $141K/yr

The Opportunity The CRA II will assist in the clinical execution and management of all aspects of ... Conduct single or multi-center medical device clinical studies. * Perform study site visits (SQV ...

Abbott

Clinical Research Associate I

Alameda, CA · On-site

... CRA/CRC/CTA experience; or combination of some education and minimum 2 yrs experience will be considered. * Experience in conducting medical device studies and/or in-vitro diagnostics studies ...

Abbott

Clinical Research Associate

Alameda, CA · On-site

$73K - $116K/yr

... a CRA/CRC/CTA experience, or combination of appropriate education and experience. * Experience working on medical device studies and/or in-vitro diagnostics studies preferred. Pharmaceutical ...

Abbott

Clinical Research Associate II

Alameda, CA

$81K - $141K/yr

The Opportunity The CRA II will assist in the clinical execution and management of all aspects of ... Conduct single or multi-center medical device clinical studies. * Perform study site visits (SQV ...

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Showing results 1-20

All JobsMedical Device Cra JobsMedical Device Cra Jobs in California

Medical Device Cra information

See California salary details

$10.9K

$78.4K

$135.7K

How much do medical device cra jobs pay per year?

As of Sep 2, 2026, the average yearly pay for medical device cra in California is $78,396.00, according to ZipRecruiter salary data. Most workers in this role earn between $32,600.00 and $134,700.00 per year, depending on experience, location, and employer.

What is a medical device CRA?

Medical Device Clinical Research Associates (CRAs) are professionals who oversee and monitor clinical trials involving medical devices to ensure compliance with regulatory requirements and study protocols. They work closely with clinical sites, investigators, and sponsors to verify data accuracy, patient safety, and the proper conduct of the trial. CRAs play a critical role in ensuring that the medical device under investigation is tested ethically and effectively before it reaches the market.

What skills and qualifications are needed to be a medical device CRA?

To thrive as a Medical Device CRA, you need a solid background in life sciences or healthcare, knowledge of clinical trial processes, and typically a bachelor's degree in a related field. Familiarity with electronic data capture (EDC) systems, regulatory guidelines (such as GCP and ISO 14155), and sometimes certifications like ACRP or SOCRA are highly valued. Strong attention to detail, effective communication, and organizational skills help CRAs manage site relationships and ensure compliance. These skills are crucial for maintaining study integrity, meeting regulatory requirements, and safeguarding patient safety throughout clinical trials.

What challenges do medical device CRAs face during clinical trials?

Medical Device CRAs often encounter challenges such as ensuring protocol compliance across multiple clinical sites, managing complex documentation requirements, and adapting to frequent regulatory updates. They must also facilitate effective communication between sponsors, investigators, and site staff to maintain trial integrity. Balancing frequent travel with timely data monitoring and issue resolution is another typical aspect of the role, requiring strong organizational and interpersonal skills.

What is the difference between Medical Device Cra vs Clinical Research Associate?

AspectMedical Device CraClinical Research Associate
CertificationsRegulatory knowledge, industry-specific certificationsGCP, ICH certifications, clinical trial training
Work EnvironmentMedical device companies, regulatory agenciesPharmaceutical companies, clinical trial sites
Industry UsageMedical device development and testingDrug and pharmaceutical trials
Common Search/ComparisonRegulatory compliance, device testingTrial monitoring, patient safety

Both roles involve overseeing clinical trials, but Medical Device Cras focus on medical device testing and regulatory compliance, while Clinical Research Associates primarily monitor drug trials and ensure adherence to protocols. Understanding these differences helps professionals choose the right career path or job search focus within clinical research.

What are popular job titles related to Medical Device Cra jobs in California?

For Medical Device Cra jobs in California, the most frequently searched job titles are:

What job categories do people searching Medical Device Cra jobs in California look for?

The top searched job categories for Medical Device Cra jobs in California are:

What cities in California are hiring for Medical Device Cra jobs?

Cities in California with the most Medical Device Cra job openings:

Medical Device Cra jobs near you
Infographic showing various Medical Device Cra job openings in California as of August 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 100% In-person job distribution, with an average salary of $78,396 per year, or $37.7 per hour.

Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)

Medpace, Inc.

San Francisco, CA • Remote

$60K - $140K/yr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 9 days ago

Medpace rating

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

14th of 74 rated research

Job description

Job Summary
Clinical Research Coordinators wanted at Medpace! Become a CRA and join our growing team!
This is an exciting home-based opportunity for clinical research professionals with at least two years of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace. Through our PACE® Training Program, you will receive the training needed to become a fully resourced CRA. You will also have the opportunity to earn a generous travel bonus, in addition to a competitive salary.
We Offer the Following:
  • Competitive travel bonus
  • Equity/Stock option program
  • Training completion and retention bonus
  • Annual merit increases
  • 401K matching
  • Opportunity to work from home
  • Flexible work hours across days within a week
  • Retain airline reward miles and hotel reward points
  • Home office furniture allowance, laptop, mobile phone with hotspot for internet access anywhere
  • In-house travel agents, reimbursement for airline club membership, and TSA pre-check
  • Opportunity for leadership positions - Lead CRA, CRA Manager, Training and Development Manager, and many more
  • CRA training program - PACE®
  • Ongoing therapeutic training by our in-house physicians who are medical and regulatory experts
  • In-house administrative support for all levels of CRA
  • Opportunity to work with international team of CRAs

Responsibilities
  • Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol
  • Communication with the medical site staff including coordinators, clinical research physicians, and their site staff
  • Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff
  • Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements
  • On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward
  • Verification the investigator is enrolling only eligible subjects
  • Regulatory document review
  • Medical device and/or investigational product/drug accountability and inventory
  • Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol
  • Assess the clinical research site's patient recruitment and retention success and offering suggestions for improvement
  • Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance

Qualifications
  • Minimum of a Bachelor's degree in a health or science related field
  • Experience as a Clinical Research Coordinator (minimum 2 years)
  • Ability to travel 60-70% to locations nationwide is required; some visits may be conducted remotely
  • A valid driver's license and the ability to drive to monitoring sites
  • Proficient knowledge of Microsoft Office
  • Strong communication and presentation skills
  • Detail-oriented and efficient in time management

Compensation
A target salary range of $60,000 - $140,000 with potential for bonus and equity awards. Your compensation will be based on your skills and experience. Medpace offers the following benefits for full-time positions: medical, dental, vision, 401(k), vacation policy, sick days, paid holidays, work from home flexibility, short-term disability, long-term disability, health savings and flexible savings accounts, life and AD&D insurance, pet insurance, and reimbursement for travel expenses (including food and gas allowance, rental cars, and hotel accommodations). For more details, please discuss with your recruiter.
#LI-Remote
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.
Why Medpace?
When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Purpose-Driven Work
    • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture
    • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
    • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development
    • Office based environment with on-site mentors
    • Defined career paths with clear advancement opportunities
    • Industry renowned onboarding and training programs designed to accelerate professional development
    • Ongoing training and continuous learning opportunities throughout your career
    • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits
    • Competitive compensation programs that recognize and reward performance
    • Comprehensive health, wellness, retirement, and PTO benefits
    • Office based culture with occasional WFH that provides flexibility for eligible positions after training
    • Company-sponsored social events

Please note benefits may vary based on country.
What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

What Medpace employees say

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About Medpace

Sourced by ZipRecruiter

Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Cincinnati, OH, US

Year founded

1992

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