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Clinical Research Associate Jobs in San Ramon, CA

RD Partners

Research Associate I

Foster City, CA · On-site

$39.85/hr

R&D Partners is seeking to hire a Research Associate I in Foster City, CA . Your main ... Scientific, Clinical Research and Engineering. Our team offers well over 200 years of combined ...

Abbott

Clinical Research Associate I

Alameda, CA · On-site

$73K - $116K/yr

What You'll Work On * Perform internal clinical studies, recruit study participants, conduct ... Research and Discovery DIVISION: ADC Diabetes Care LOCATION: United States > Alameda : Plaza 6 ...

Abbott

Clinical Research Associate I

Alameda, CA

$73K - $116K/yr

What You'll Work On * Perform internal clinical studies, recruit study participants, conduct ... Research and Discovery DIVISION: ADC Diabetes Care LOCATION: United States > Alameda : Plaza 6 ...

Abbott

Clinical Research Associate I

Alameda, CA · On-site

$73K - $116K/yr

As the Clinical Research Associate I you will assist in the clinical execution and management of all aspects of assigned clinical studies. This includes but not limited to planning and implementation ...

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All JobsClinical Research Associate JobsClinical Research Associate Jobs in San Ramon, CA

Clinical Research Associate information

See San Ramon, CA salary details

$13

$45

$77

How much do clinical research associate jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for clinical research associate in San Ramon, CA is $45.96, according to ZipRecruiter salary data. Most workers in this role earn between $32.26 and $58.85 per hour, depending on experience, location, and employer.

Is it hard to get a clinical research associate job?

Securing a clinical research associate (CRA) position can be competitive, often requiring a relevant degree such as a life sciences or healthcare-related field, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and familiarity with clinical trial management systems can improve job prospects, but entry may be challenging for those without relevant qualifications or experience.

What is a clinical research associate?

Clinical Research Associates (CRAs) are professionals responsible for monitoring and overseeing clinical trials to ensure they are conducted in accordance with regulatory guidelines, protocols, and ethical standards. They play a key role in ensuring the safety of trial participants and the integrity of collected data. CRAs often visit clinical trial sites to verify data accuracy, maintain study documentation, and provide training to site staff. Their work ensures that new drugs, treatments, or medical devices are tested rigorously before they reach the market.

What are the key skills and qualifications needed to thrive as a clinical research associate?

To thrive as a Clinical Research Associate, you need a solid background in life sciences, attention to detail, and experience with clinical trial protocols, often supported by a relevant bachelor's degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and sometimes certifications like ACRP or SOCRA is typically required. Strong organizational, communication, and problem-solving skills help build effective relationships with research sites and ensure compliance. These skills are vital for maintaining the integrity of clinical trials, ensuring regulatory adherence, and advancing medical research efficiently.

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

AspectClinical Research AssociateClinical Trial Coordinator
CredentialsBachelor's degree, often with clinical research certificationsBachelor's degree, often with clinical research or healthcare certifications
Work EnvironmentMonitors clinical sites, reviews data, ensures complianceCoordinates trial activities, manages schedules, and communicates with sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, CROs

Both roles are essential in clinical trials, with CRAs focusing on site monitoring and compliance, while Clinical Trial Coordinators handle day-to-day trial management. They often collaborate but have distinct responsibilities within the clinical research process.

Is being a clinical research associate worth it?

A clinical research associate (CRA) monitors clinical trials to ensure compliance with protocols and regulations, often requiring strong organizational and communication skills. The role offers opportunities for career growth, competitive salaries, and the chance to contribute to medical advancements, but it can involve irregular hours and travel. Overall, it can be a rewarding career for those interested in healthcare and research.

What are some common challenges clinical research associates face when monitoring clinical trial sites?

Clinical Research Associates (CRAs) often encounter challenges such as ensuring protocol compliance across multiple sites, managing tight project timelines, and maintaining accurate documentation. Additionally, CRAs must effectively communicate with site staff to resolve issues and ensure data integrity, all while adhering to regulatory guidelines. Balancing frequent travel, adapting to different site environments, and handling unexpected issues such as patient recruitment delays are also typical aspects of the role.
More about Clinical Research Associate jobs
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What job categories do people searching Clinical Research Associate jobs in San Ramon, CA look for? The top searched job categories for Clinical Research Associate jobs in San Ramon, CA are:
What cities near San Ramon, CA are hiring for Clinical Research Associate jobs? Cities near San Ramon, CA with the most Clinical Research Associate job openings:
Clinical Research Associate jobs near you
Infographic showing various Clinical Research Associate job openings in San Ramon, CA as of August 2026, with employment types broken down into 2% As Needed, 71% Full Time, 21% Part Time, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $95,595 per year, or $46 per hour.

Senior Clinical Research Associate

Epicrispr Biotechnologies

South San Francisco, CA • On-site

$115K - $121K/yr

Other

Re-posted 2 days ago

Job description

Position: Senior Clinical Research Associate

Location: South San Francisco, CA

Opportunity:
Epicrispr Bio is seeking a detail-oriented and proactive Senior Clinical Research Associate (CRA) to support the execution and oversight of clinical trials. This role will play a key part in ensuring studies are conducted in compliance with regulatory requirements, GCP guidelines, and company protocols, while maintaining the highest standards of quality and data integrity.

The ideal candidate will bring a strong foundation in clinical operations, experience working cross-functionally with CROs and clinical teams, and the ability to independently manage site activities while contributing to process improvements in a fast-paced, growing environment. This is an opportunity to have meaningful impact on clinical development programs while helping to build and scale operational excellence within the organization.

Roles and Responsibilities:

  • Assist the Clinical Operations team with on-site sample operations, including sample receipt, registration, and shipments in a GCP environment.
  • Support clinical trial manager with site management, including: site startup activities, co-monitoring visits alongside CRO, reviewing monitoring visit reports, coordinating vendor trainings, reviewing study newsletters, and other duties as needed, in alignment with study priorities and CTM guidance.
  • Assist clinical trial manager with data verification and ICF reviews as needed, alongside CRO, to support data quality and protocol compliance.
  • Partner with CTM and clinical team to help identify areas to improve our processes, with priorities defined by the CTM, and support implementation of agreed-upon improvements.
  • Identify and communicate site-level issues, protocol deviations, and operational risks to the CTM to support timely resolution.
  • Maintain study trackers, logs, and documentation across regulatory, site, data, and sample operations to support study oversight and execution.

Qualifications:

  • Bachelor's degree in life sciences or related field preferred
  • 2 - 5+ years of CRA or clinical research experience (biotech, pharma, or CRO environment)
  • Strong understanding of GCP, ICH guidelines, and clinical trial processes
  • Experience working with CROs and managing clinical sites
  • Excellent organizational, communication, and problem-solving skills
  • Ability to manage multiple priorities in a fast-paced environment

Compensation: The salary range for this position is $115,000 to $121,000 USD annually. This salary range is an estimate, and the actual salary may vary based on various factors, including, without limitation, individual education, experience, tenure, skills, and abilities, as well as internal equity and alignment with market data, including potential adjustments for geographic location. 

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