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Clinical Study Assistant Jobs in California (NOW HIRING)

Abbott

Director, Clinical Research (Lingo)

Alameda, CA · On-site

Manage a clinical study team that may include Clinical Research Associates, Senior Clinical Research Associates, and Clinical Study Assistants. Provide guidance, team building, and professional ...

Masimo Corporation

Clinical Research Lab RN II

Irvine, CA · On-site

$55 - $72/hr

The individual in this position is responsible for assigned clinical trial projects undertaken in ... An advanced individual may assist with/conduct more complicated studies, as well as contribute to ...

New

Masimo

Clinical Research Lab RN II

Irvine, CA · On-site

$40 - $52/hr

The individual in this position is responsible for assigned clinical trial projects undertaken in ... An advanced individual may assist with/conduct more complicated studies, as well as contribute to ...

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Clinical Study Assistant information

See California salary details

$11

$19

$28

How much do clinical study assistant jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for clinical study assistant in California is $19.97, according to ZipRecruiter salary data. Most workers in this role earn between $16.35 and $23.03 per hour, depending on experience, location, and employer.

What is a clinical study assistant?

Clinical Study Assistants are professionals who support the conduct of clinical trials by handling administrative tasks, maintaining study documentation, and ensuring regulatory compliance. They work closely with clinical research teams to coordinate schedules, communicate with study sites, and help manage trial materials. Their role is crucial in ensuring that clinical studies run smoothly, efficiently, and according to protocols and regulatory guidelines.

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

To thrive as a Clinical Study Assistant, you need strong organizational skills, attention to detail, and a background in life sciences or related fields, often supported by a bachelor's degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and regulatory documentation processes is typically required. Effective communication, teamwork, and problem-solving skills help you navigate complex study protocols and collaborate with diverse stakeholders. These abilities are crucial for ensuring the accuracy, compliance, and smooth operation of clinical research studies.

What are the main challenges a clinical study assistant might face when supporting clinical trial operations?

A Clinical Study Assistant often encounters challenges such as managing multiple tasks under tight deadlines, ensuring accurate documentation, and coordinating communication between research teams, sponsors, and regulatory bodies. Additionally, adapting to evolving study protocols and maintaining compliance with strict regulatory requirements can be demanding. Strong organizational skills, attention to detail, and proactive communication are essential for navigating these challenges successfully.

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

AspectClinical Study AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related fieldUsually requires a bachelor's degree, often with additional certifications in clinical research
Work EnvironmentSupports clinical trials in hospitals, research centers, or pharmaceutical companiesManages entire clinical studies, coordinating between sites, staff, and sponsors
Employer & IndustryHospitals, research institutions, pharmaceutical companiesAcademic medical centers, hospitals, research organizations
Search & Comparison IntentOften compared for entry-level roles supporting clinical trialsCompared for roles with broader responsibilities in clinical study management

The Clinical Study Assistant primarily supports clinical trial activities by assisting with data collection and documentation, while the Clinical Research Coordinator manages the overall conduct of the study, including patient recruitment and compliance. Both roles require similar educational backgrounds but differ in scope and responsibilities within the clinical research process.

What are the most commonly searched types of Clinical Study jobs in California?

The most popular types of Clinical Study jobs in California are:

What cities in California are hiring for Clinical Study Assistant jobs?

Cities in California with the most Clinical Study Assistant job openings:

Clinical Study Assistant jobs near you
Infographic showing various Clinical Study Assistant job openings in California as of August 2026, with employment types broken down into 2% As Needed, 71% Full Time, 18% Part Time, and 9% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $41,528 per year, or $20 per hour.

Director, Clinical Research (Lingo)

Abbott

Alameda, CA • On-site

Full-time

Medical, Retirement

Re-posted 17 days ago

Key responsibilities

  • Design, plan, develop, monitor, and execute all clinical research activities within the Lingo Division.

  • Manage a clinical study team, providing guidance, team building, and professional development.

  • Evaluate and interpret clinical research data to ensure accurate analysis and interpretation.

Abbott rating

7.8

Company rating: 7.8 out of 10

Based on 138 frontline employees who took The Breakroom Quiz

170th of 545 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:
ABOUT LINGO:
Abbott's rich history in developing cutting-edge health technologies is evolving with its new venture into biowearables. The biowearables segment is poised to represent the future of the organization, with the potential to generate over $1 billion in revenue within the next five years, supported by Abbott's robust R&D and financial resources.
At Lingo, we are committed to transforming health management with our cutting-edge biowearables that monitor glucose levels and other critical metabolic biomarkers. Our products integrate world-class heath technology with the best of biological and behavioral to provide personalized insights that improve metabolic well-being. This is your opportunity to be at the forefront of health innovation and make a significant impact on people's lives.
WORKING AT ABBOTT:
At Abbott, you can do work that matters, grow, and learn, care for yourself and 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.
  • An excellent retirement savings plan with 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 around the world 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 a best place to work for diversity, working mothers, female executives, and scientists.

THE OPPORTUNITY:
We are seeking an experienced Director of Clinical Research to lead the strategic planning, execution, and oversight of Lingo's clinical research programs. You will be responsible for applying clinical best practices, regulations, and quality standards for successful planning and execution of a clinical research program that includes internal studies, investigator-initiated studies, real world evidence and studies done with external partners to evaluate safety and efficacy.
This position will be required to manage multiple projects simultaneously and meet targeted timelines while strategizing for issue resolution and study execution. You will need to partner and develop working relationships with new clinical sites, vendors, CROs and KOLs.
WHAT YOU'LL WORK ON:
  • Direct the design, planning, development, monitoring and execution of all clinical research activities within the Lingo Division.
  • Manage a clinical study team that may include Clinical Research Associates, Senior Clinical Research Associates, and Clinical Study Assistants. Provide guidance, team building, and professional development for direct reports.
  • Evaluate and interpret clinical research data to ensure timely, accurate analysis and interpretation.
  • Contribute to the development of strategic goals and the preparation of clinically and scientifically sound publications, manuscripts, abstracts, and presentations.
  • Demonstrate strong leadership and coaching skills to build effective relationships within the team and across the Division.
  • Manage the development of clinical trial protocols, final reports, clinical brochures, and the negotiation and execution of clinical site agreements.
  • Prepare Clinical Project Charters outlining timelines, budgets, and personnel requirements, ensuring projects operate within approved scope and budget.
  • Align functional goals with the Division's long-term business needs and strategic objectives.
  • Maintain, promote, and model social, ethical, and organizational norms and ensure adherence to compliance standards and ethical principles.
  • Collaborate with internal (e.g., Product, Marketing, Medical Affairs, Regulatory, Quality, and Legal) and external (e.g., Principal Investigators, Key Opinion Leaders) partners to execute strategic initiatives.

REQUIRED QUALIFICATIONS:
  • Bachelor's degree in a related scientific or medical field required
  • Master's degree, PhD, MD, or DO strongly preferred
  • Minimum of 10 years of related clinical research experience
  • Demonstrated experience designing and conducting randomized controlled trials
  • Strong understanding of the scientific method and its application to well controlled clinical evaluations
  • Proven leadership experience managing and developing clinical research teams

Skills & Competencies:
• Deep knowledge and expertise in clinical research design research and execution
• Content expertise in the metabolic health space
• Strong project management, budgeting, and organizational skills
• Excellent written, verbal, and presentation skills
• Ability to communicate effectively with cross-functional stakeholders and external regulatory agencies
• Strong collaborative skills and experience working in matrixed organizations
• Strategic thinker with the ability to manage multiple priorities in a fast-paced environment
APPLY NOW:
Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal
The base pay for this position is
$172,000.00 - $344,000.00
In specific locations, the pay range may vary from the range posted.
JOB FAMILY:
Clinical Affairs / Statistics
DIVISION:
LNGO Lingo
LOCATION:
United States > Alameda : 2601 Harbor Bay Parkway
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
Not specified
MEDICAL SURVEILLANCE:
Not Applicable
SIGNIFICANT WORK ACTIVITIES:
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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