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Clinical Project Associate Jobs in California (NOW HIRING)

To lead the process of clinical project feasibility during standalone feasibility (awarded ... Collecting data from data assets as well as country associates, site level Investigators, and KOL ...

Clinical Trial Assistant

Sunnyvale, CA · On-site

$70K - $94K/yr

Collaborate with Clinical Research Associates (CRA), Clinical Study Managers (CSM) and Clinical ... Prior experience in medical device clinical trials, regulatory support, clinical project ...

Clinical Trial Assistant

Sunnyvale, CA · On-site

$70K - $94K/yr

Collaborate with Clinical Research Associates (CRA), Clinical Study Managers (CSM) and Clinical ... Prior experience in medical device clinical trials, regulatory support, clinical project ...

Clinical Trial Assistant

Sunnyvale, CA · On-site

$70K - $94K/yr

Collaborate with Clinical Research Associates (CRA), Clinical Study Managers (CSM) and Clinical ... Prior experience in medical device clinical trials, regulatory support, clinical project ...

Clinical Trial Assistant

Sunnyvale, CA · On-site

$70K - $94K/yr

Collaborate with Clinical Research Associates (CRA), Clinical Study Managers (CSM) and Clinical ... Prior experience in medical device clinical trials, regulatory support, clinical project ...

Showing results 41-60

Clinical Project Associate information

See California salary details

$12

$31

$54

How much do clinical project associate jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for clinical project associate in California is $31.13, according to ZipRecruiter salary data. Most workers in this role earn between $20.87 and $41.06 per hour, depending on experience, location, and employer.

What is a clinical project associate?

A Clinical Project Associate (CPA) is a professional who supports the planning, execution, and management of clinical trials in the pharmaceutical, biotechnology, or medical device industries. Their responsibilities often include coordinating study documentation, assisting with regulatory submissions, tracking project timelines, and facilitating communication among study teams. CPAs play a crucial role in ensuring that clinical trials are conducted efficiently, ethically, and in compliance with regulatory standards. They work closely with clinical project managers, research associates, and other team members to help bring new therapies and treatments to market.

What are the typical responsibilities of a clinical project associate?

As a Clinical Project Associate, you will play a vital role in ensuring the smooth execution of clinical trials by handling administrative and logistical tasks. Your responsibilities often include maintaining study documentation, coordinating meetings, tracking project timelines, and supporting communication between internal teams and external partners such as clinical sites and vendors. You may also assist with regulatory submissions and help monitor compliance with study protocols. This position offers excellent exposure to the clinical research process and can be a stepping stone to more advanced roles within clinical operations.

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

To thrive as a Clinical Project Associate, you need a background in life sciences or a related field, attention to detail, and strong organizational skills. Familiarity with clinical trial management systems (CTMS), regulatory documentation, and tools like Microsoft Office is typically required. Excellent communication, teamwork, and time management abilities help professionals excel in supporting project coordination. These skills are crucial for ensuring regulatory compliance, smooth project execution, and effective collaboration within clinical research teams.

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

AspectClinical Project AssociateClinical Research Coordinator
CredentialsBachelor's degree often required; certifications like CCRP beneficialBachelor's degree in health or related field; certifications like CCRP common
Work EnvironmentTypically works with project teams, sponsors, and CROs in clinical trial settingsWorks directly with patients, investigators, and site staff at clinical trial sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, clinics, research sites
Search & Comparison IntentHigh overlap in responsibilities and certificationsSimilar roles but more patient-facing

The Clinical Project Associate primarily supports clinical trial management from a project perspective, working with sponsors and CROs. In contrast, the Clinical Research Coordinator focuses on patient interactions and site management. Both roles require similar educational backgrounds and certifications, but their work environments and daily tasks differ significantly.

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

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

What job categories do people searching Clinical Project Associate jobs in California look for?

The top searched job categories for Clinical Project Associate jobs in California are:

What cities in California are hiring for Clinical Project Associate jobs?

Cities in California with the most Clinical Project Associate job openings:

Infographic showing various Clinical Project Associate 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 $64,745 per year, or $31.1 per hour.

Director, Clinical Research (Lingo)

Alameda, CA

Full-time

Medical, Retirement

Re-posted 28 days ago


Abbott rating

7.8

Company rating: 7.8 out of 10

Based on 139 frontline employees who took The Breakroom Quiz


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 / StatisticsDIVISION:LNGO LingoLOCATION:United States > Alameda : 2601 Harbor Bay ParkwayADDITIONAL LOCATIONS:WORK SHIFT:StandardTRAVEL:Not specifiedMEDICAL SURVEILLANCE:Not ApplicableSIGNIFICANT 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.pdfEEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

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