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Clinical Data Associate Jobs in San Ramon, CA (NOW HIRING)

Abbott

Clinical Research Associate II

Alameda, CA · On-site

$81K - $141K/yr

Clinical Research Associate II Working at Abbott At Abbott, you can do work that matters, grow, and ... Perform review of clinical data listings for completeness and accuracy, and escalate issues to the ...

Abbott

Clinical Research Associate I

Alameda, CA · On-site

Perform review of clinical data listings for completeness and accuracy; and escalate issues to the Clinical Operations Manager/Study Lead as needed. * Proactively and effectively communicate the ...

Deloitte

Senior Manager Data Lead

San Jose, CA · On-site

Work You'll Do As an Associate Vice President, AI and Data Solutions on the AI & Data team, you ... Clinical data exchange and coding standards, including HL7, FHIR, and ICD * Data operations (ie ...

Deloitte

Senior Manager Data Lead

San Francisco, CA · On-site

Work You'll Do As an Associate Vice President, AI and Data Solutions on the AI & Data team, you ... Clinical data exchange and coding standards, including HL7, FHIR, and ICD * Data operations (ie ...

Abbott

Clinical Research Associate I

Alameda, CA · On-site

The Opportunity The CRA will ensure quality, accuracy and integrity of clinical trial data throughout the full lifecycle of multiple clinical trials according to the Code of Federal Regulations, ICH ...

Abbott

Clinical Research Associate I

Alameda, CA

The Opportunity The CRA will ensure quality, accuracy and integrity of clinical trial data throughout the full lifecycle of multiple clinical trials according to the Code of Federal Regulations, ICH ...

Exelixis

Associate Biostatistics Director

Alameda, CA · On-site

$166K - $236K/yr

Works collaboratively with clinicians, data managers, biostatisticians, statistical programmers, and medical writers in the planning, conduct and analysis of clinical trials. Essential Duties And ...

Abbott

Clinical Research Associate

Alameda, CA · On-site

$73K - $116K/yr

Clinical Research Associate I Working at Abbott At Abbott, you can do work that matters, grow, and ... The Opportunity The CRA will ensure quality, accuracy, and integrity of clinical trial data ...

Exelixis

Associate Biostatistics Director

Alameda, CA · On-site

$166K - $236K/yr

Works collaboratively with clinicians, data managers, biostatisticians, statistical programmers, and medical writers in the planning, conduct and analysis of clinical trials. Essential Duties And ...

Exelixis

Associate Biostatistics Director

Alameda, CA · On-site

$166K - $236K/yr

Works collaboratively with clinicians, data managers, biostatisticians, statistical programmers, and medical writers in the planning, conduct and analysis of clinical trials. Essential Duties And ...

Abbott

Clinical Research Associate

Alameda, CA · On-site

$73K - $116K/yr

Clinical Research Associate I Working at Abbott At Abbott, you can do work that matters, grow, and ... The Opportunity The CRA will ensure quality, accuracy, and integrity of clinical trial data ...

Abbott

Clinical Research Associate II

Alameda, CA

$81K - $141K/yr

... data to drive better-informed decisions. We're revolutionizing the way people monitor their glucose levels with our new sensing technology. As the Clinical Research Associate II, you will assist in ...

Abbott

Clinical Research Associate II

Alameda, CA

$81K - $141K/yr

... data to drive better-informed decisions. We're revolutionizing the way people monitor their glucose levels with our new sensing technology. As the Clinical Research Associate II, you will assist in ...

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

Clinical Data Associate information

See San Ramon, CA salary details

$15

$43

$96

How much do clinical data associate jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for clinical data associate in San Ramon, CA is $43.53, according to ZipRecruiter salary data. Most workers in this role earn between $32.79 and $43.51 per hour, depending on experience, location, and employer.

What does a clinical data associate do?

A Clinical Data Associate is responsible for collecting, validating, and managing clinical trial data to ensure its accuracy, completeness, and compliance with regulatory standards. They work closely with clinical research teams to monitor data quality, resolve discrepancies, and prepare data for analysis. Their work is essential in supporting drug development and regulatory submissions by ensuring reliable and high-quality clinical data.

What does a clinical data associate do?

A clinical data associate is responsible for tracking data and results in a research study. As a clinical data associate, your job duties are to collect data, perform data management, and input data into any software used by your team. You work on a research team, so you must be able to work collaboratively and have excellent organizational skills. While you spend most of your time in an office, you may be required to work in the field to record data. The only universal qualifications needed for this career are a background in health care or medical science research and experience with data management software like Oracle Clinical, Microsoft Excel, and SPSS.

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

To thrive as a Clinical Data Associate, you need a solid understanding of clinical research, data management principles, and attention to detail, often supported by a degree in life sciences or a related field. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of regulatory guidelines like GCP or CDISC is typically required. Strong organizational skills, analytical thinking, and clear communication set outstanding candidates apart in this role. These skills ensure the accuracy, integrity, and compliance of clinical trial data, which are crucial for successful research outcomes and regulatory approval.

What are some common challenges faced by clinical data associates when ensuring data quality during clinical trials?

Clinical Data Associates often encounter challenges such as identifying and resolving discrepancies in large datasets, maintaining strict compliance with regulatory standards, and coordinating timely data entry from multiple sites. They must work closely with clinical research teams and data managers to clarify ambiguous data and implement data cleaning procedures. Staying organized and detail-oriented is essential to ensure data accuracy and the successful progression of clinical trials.

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

AspectClinical Data AssociateClinical Research Coordinator
Primary RoleManage and ensure accuracy of clinical trial dataOversee trial operations, patient recruitment, and site management
CredentialsBachelor's in life sciences or related field; familiarity with data managementBachelor's in health sciences or related field; clinical trial experience
Work EnvironmentData management teams, clinical trial databasesClinical sites, hospitals, research facilities
Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites

While both roles support clinical trials, a Clinical Data Associate primarily focuses on managing and validating trial data, ensuring accuracy and compliance. In contrast, a Clinical Research Coordinator handles the overall trial operations, including patient recruitment and site coordination. Both roles require relevant certifications and work within the clinical research industry, but their daily responsibilities differ significantly.

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The most popular types of Clinical Data jobs in San Ramon, CA are:

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For Clinical Data Associate jobs in San Ramon, CA, the most frequently searched job titles are:

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Clinical Data Associate jobs near you
Infographic showing various Clinical Data Associate job openings in San Ramon, CA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 50% In-person, and 50% Hybrid job distribution, with an average salary of $90,542 per year, or $43.5 per hour.

Clinical Research Associate II

Abbott

Alameda, CA • On-site

$81K - $141K/yr

Full-time

Medical, Retirement

Re-posted 24 days ago

Abbott rating

7.8

Company rating: 7.8 out of 10

Based on 138 frontline employees who took The Breakroom Quiz

171st of 546 rated manufacturers

Job description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries.
JOB DESCRIPTION:
Clinical Research Associate II
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have access to:
  • Career development with an international company where you can grow the career you dream of.
  • Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
  • An excellent retirement savings plan with a high employer contribution.
  • Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree.
  • A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.
  • A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity
The CRA II will assist in the clinical execution and management of all aspects of assigned clinical studies. This includes but not limited to planning and implementation of clinical studies from concept to clinical study report per timelines and quality standards.
This position will be based in our Alameda, CA office.
What You'll Work On
  • Conduct single or multi-center medical device clinical studies.
  • Perform study site visits (SQV, SIV, IMV, COV), generate monitoring trip reports, and track resolution of action items.
  • Participate in study start up activities.
  • Responsible for shipping study devices and supplies to clinical sites and performing study device accountability.
  • Manage clinical monitoring activities and overall site management ensuring compliance to the Study Protocol, Good Clinical Practices (GCPs), ICH guidelines, Federal Regulations, department procedures and applicable regulatory requirements.
  • Responsible for assisting senior staff in planning study conduct, designing case report forms (CRFs), conducting User Acceptance Testing (UAT), Contract Research Organization (CRO) selection and management, selection and training of investigator sites, planning and running study meetings, evaluation, selection and training of new study investigators and writing and assembling submissions.
  • Maintain and audit Trial Master File to ensure inspection readiness.
  • Perform review of clinical data listings for completeness and accuracy, and escalate issues to the Clinical Operations Manager as needed.
  • Participate in cross-functional clinical team(s) in the planning and execution of clinical trials.
  • Proactively and effectively communicate the status of clinical studies to management.
  • Ensures quality delivery of study deliverables within agreed budgets and timelines.
  • Participate in the interim and final reviews of study data in preparation of regulatory submissions.
  • Involved in the preparation of all applicable documents required for the conduct of the study (such as Trial Master File (TMF), Clinical Protocols and Reports).
  • May interact with RA/QA in responding to audits and FDA inquiries.

Required Qualifications
  • B.S. degree in life sciences or equivalent with minimum 5 years of clinical research experience.
  • Must have 2+ years of relevant experience in site monitoring.
  • Experience in conducting medical device and/or in-vitro diagnostics studies preferred. Pharmaceutical background may also be considered.
  • Must be able to travel 30-50%.

Preferred Qualifications
  • Demonstrated excellence in teamwork, shared mindset for success, stellar interpersonal and communication skills including building rapport with team members, peers, and management.
  • Solid understanding and demonstrated experience of the clinical trial process including study design and conduct; clinical data management systems; clinical trial management systems; data analysis; and data reporting and interpretation.
  • Must have a demonstrated ability to solve problems with innovative solutions along with strong project management and organizational skills to deliver projects on time and on budget.
  • Able to manage numerous projects/conflicting priorities, and to be flexible when priorities change.
  • Working knowledge of GCP, Clinical and Regulatory Affairs.
  • Proficient with Microsoft Suite.

The base pay for this position is
$81,500.00 - $141,300.00
In specific locations, the pay range may vary from the range posted.
JOB FAMILY:
Medical & Scientific Affairs
DIVISION:
ADC Diabetes Care
LOCATION:
United States > Alameda : Plaza 6 Building
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
Yes, 25 % of the Time
MEDICAL SURVEILLANCE:
No
SIGNIFICANT WORK ACTIVITIES:
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday)
Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf
EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

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