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Clinical Research Assistant Jobs in San Ramon, CA

Flourish Research

Research Assistant

Walnut Creek, CA · On-site

$250/hr

About Us Flourish Research is where clinical trials thrive.Flourish Research is one of the industry ... About the Job We are actively hiring a Research Assistant to supportour Walnut Creek, California ...

Flourish Research

Research Assistant

Walnut Creek, CA · On-site

$21 - $22/hr

About Us: Flourish Research is where clinical trials thrive. Flourish Research is one of the ... We are actively hiring a Research Assistant to support our Walnut Creek, California site. Shift:

Flourish Research

Research Assistant

Walnut Creek, CA · On-site

$21 - $22/hr

About Us: Flourish Research is where clinical trials thrive. Flourish Research is one of the ... We are actively hiring a Research Assistant to support our Walnut Creek, California site. Shift:

Flourish Research

Research Assistant

Walnut Creek, CA · On-site

$21 - $22/hr

About Us: Flourish Research is where clinical trials thrive. Flourish Research is one of the ... We are actively hiring a Research Assistant to support our Walnut Creek, California site. Shift:

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

Clinical Research Assistant information

See San Ramon, CA salary details

$9

$25

$51

How much do clinical research assistant jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for clinical research assistant in San Ramon, CA is $25.38, according to ZipRecruiter salary data. Most workers in this role earn between $19.33 and $28.99 per hour, depending on experience, location, and employer.

What is a clinical research assistant?

Clinical Research Assistants are professionals who support clinical research studies by performing a range of administrative and research-related tasks. They help collect and manage data, assist with patient recruitment, prepare study materials, and ensure compliance with research protocols and regulations. Their work is crucial in advancing medical knowledge and ensuring that clinical trials run smoothly and ethically. Clinical Research Assistants often work under the supervision of principal investigators or clinical research coordinators in hospitals, universities, or pharmaceutical companies.

What does a clinical research assistant do?

A clinical research assistant—or clinical research associate (CRA)—helps lead researchers during clinical trials for new drugs and medical devices. As a clinical research assistant, your responsibilities include preparing the laboratory, processing volunteers, taking biological samples or vital signs, and organizing data. You may also be required to set up and clean work areas. Your job is to assist the researchers in any way possible, helping them conduct sound, ethical, and scientifically accurate research.

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

To thrive as a Clinical Research Assistant, you need a bachelor’s degree in a life science or health-related field, attention to detail, and strong organizational skills. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and good clinical practice (GCP) certification are typically required. Excellent communication, teamwork, and problem-solving abilities help you excel in coordinating with research teams and participants. These skills ensure accurate data collection, regulatory compliance, and the smooth execution of clinical studies.

What are some common challenges clinical research assistants face when coordinating multiple studies simultaneously?

Clinical Research Assistants often manage several studies at once, which can lead to challenges in balancing competing deadlines, maintaining accurate documentation, and ensuring compliance with complex protocols. Effective time management and organizational skills are crucial to handle overlapping tasks such as scheduling patient visits, collecting data, and preparing regulatory submissions. Collaborating closely with principal investigators, coordinators, and other team members helps distribute the workload and maintain research quality. Developing strong communication habits and utilizing digital tracking tools can further streamline workflow and reduce errors.

What is the difference between Clinical Research Assistant vs Clinical Research Coordinator?

AspectClinical Research AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are a plusRequires a bachelor's degree; certifications such as CCRP or CCRC are common
Work EnvironmentAssists in data collection, patient scheduling, and administrative tasks in clinical trial settingsManages study protocols, patient recruitment, and regulatory compliance in clinical trial sites
Employer & IndustryHospitals, research institutions, pharmaceutical companiesHospitals, research centers, pharmaceutical companies

Both roles support clinical research but differ in responsibilities. Clinical Research Assistants focus on data collection and administrative tasks, while Clinical Research Coordinators oversee study management and patient interactions. Understanding these differences helps in choosing the right career path or job search focus.

Can you be a clinical research assistant with no experience?

Clinical research assistant positions often require some knowledge of medical terminology and data management, but many entry-level roles are available for candidates without prior experience. Employers may provide on-the-job training and look for strong organizational skills, attention to detail, and the ability to follow protocols. Certifications such as Good Clinical Practice (GCP) can enhance prospects for those new to the field.
More about Clinical Research Assistant jobs

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Cities near San Ramon, CA with the most Clinical Research Assistant job openings:

Clinical Research Assistant jobs near you
Infographic showing various Clinical Research Assistant job openings in San Ramon, CA as of August 2026, with employment types broken down into 2% As Needed, 72% Full Time, 19% Part Time, and 7% Contract. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $52,792 per year, or $25.4 per hour.

Research Assistant (Mandarin Bilingual) - Bay Area

Irvine Clinical Research

San Jose, CA • On-site

$25 - $27/hr

Full-time

Medical, Dental, Vision, Life, PTO

Posted 5 days ago

Job description

Oakland Clinical is part of the Irvine Clinical Research site network, the largest of its kind on the West Coast. With 5 research centers in California, we are leaders in the search for new treatments in neurology, psychiatry, and obesity medicine. Our largest area of research is in Alzheimer's Disease prevention and treatment drug trials, and our doctors were the largest contributors in the world to the most recently FDA-approved medication in Alzheimer's Disease.
As our primary site in the San Francisco Bay Area, Oakland Clinical is hiring a Bilingual Mandarin Research Assistant to support clinical trial operations and expand access to our Mandarin-speaking community. The Research Assistant serves as a crucial link between our clinical team and study participants, facilitating prescreening, study visit execution, participant reception, and bilingual translation.
Location Note: This position is initially based full-time at our Oakland clinic next to Alta Bates Summit. As our Bay Area presence grows, there may be an option for future transition to a planned South Bay location in San Jose.
Job Duties
  • Bilingual Participant Prescreening & Engagement: Conduct initial prescreening interviews in Mandarin and English to evaluate participant eligibility against study protocols, explaining trial participation in clear, accessible terms.
  • Participant Reception & Hospitality: Serve as the primary bilingual point of contact for incoming patients and study partners, providing a warm, reassuring environment and addressing cultural nuances to put families at ease.
  • Study Visit Execution & Clinical Support: Assist Clinical Research Coordinators and Investigators with participant visits, including gathering vital signs, conducting ECGs, assisting with cognitive testing logistics, and supporting lab processing as trained.
  • Bilingual Translation & Informed Consent Support: Assist with study communications, document translation, and consent discussions to ensure Mandarin-speaking participants and family partners fully understand trial procedures and requirements.
  • Data Management & Operations: Maintain meticulous source documentation, execute prompt data entry into electronic data capture (EDC) systems, and manage participant scheduling.
  • Community Outreach: Support site initiatives and community engagement within the local Mandarin-speaking population to build awareness for ongoing memory and neurology trials.

Job Requirements
  • Language Fluency: Native or full professional fluency in spoken and written Mandarin and English. Ability to communicate medical and study concepts clearly in both languages.
  • Education: Bachelor's degree in psychology, neuroscience, biology, public health, or a related scientific/healthcare discipline.
  • Preferred Clinical Experience: Prior experience in a clinical setting, medical office, or research laboratory preferred. Experience working with older adults or individuals with memory concerns is a plus.
  • Interpersonal & Cultural Competence: Strong empathy, professional demeanor, and exceptional communication skills suited for patient-facing interactions and family advocacy.
  • Detail Oriented: High organizational skills with strict attention to protocol adherence, regulatory standards, and accurate data collection.

$25 - $27 an hour
Location & Work Environment: On-site position based at our clinic next to Alta Bates Summit in Oakland (11th floor, transit accessible, multi-story parking garage, views of the bay). Potential future option for relocation to our planned San Jose location.
Schedule: Full-time, in-person schedule with no planned overnight or weekend hours.
Benefits: The company pays 100% of individual medical (Gold HMO), dental, and vision insurance premiums for eligible full-time employees. Basic life, AD&D, and long-term disability coverage are provided. Vacation (PTO) is accrued at a rate equivalent to 3 weeks per year, with separate paid sick leave.

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