This position will be required to manage multiple projects simultaneously and meet targeted ... Manage a clinical study team that may include Clinical Research Associates, Senior Clinical ...
This position will be required to manage multiple projects simultaneously and meet targeted ... Manage a clinical study team that may include Clinical Research Associates, Senior Clinical ...
Sr. Field Clinical Research Associate (SE Region) Job Title: Sr. Clinical Research Assoicate ... clinical projects. This may include, but is not limited to: * Reviewing data and source ...
Sr. Field Clinical Research Associate (SE Region) Job Title: Sr. Clinical Research Assoicate ... clinical projects. This may include, but is not limited to: * Reviewing data and source ...
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 ...
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 ...
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 ...
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 ...
Feasibility Informatics Manager
Mcfarland, CA · On-site
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 ...
Feasibility Informatics Manager
Mcfarland, CA · On-site
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 ...
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 ...
Quick apply
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 ...
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 ...
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 ...
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 ...
Quick apply
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 ...
Collaborate with Clinical Research Associates (CRA), Clinical Study Managers (CSM) and Clinical ... Prior experience in medical device clinical trials, regulatory support, clinical project ...
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 ...
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 ...
Collaborate with Clinical Research Associates (CRA), Clinical Study Managers (CSM) and Clinical ... Prior experience in medical device clinical trials, regulatory support, clinical project ...
Collaborate with Clinical Research Associates (CRA), Clinical Study Managers (CSM) and Clinical ... Prior experience in medical device clinical trials, regulatory support, clinical project ...
Sr. Clinical Research Associate (NE)
Los Angeles, CA · On-site
$70 - $75/hr
Sr. Field Clinical Research Associate Remote with Travel required in the North Central Region ... projects. * Review data and source documentation from investigational sites for accuracy and ...
Sr. Clinical Research Associate (NE)
Los Angeles, CA · On-site
$70 - $75/hr
Sr. Field Clinical Research Associate Remote with Travel required in the North Central Region ... projects. * Review data and source documentation from investigational sites for accuracy and ...
Clinical Research Associate (CRA) * Clinical Project Manager * Clinical Operations Manager * Data Manager * Biostatistician * Medical Monitor * Regulatory Affairs Specialist * Pharmacovigilance ...
Clinical Research Associate (CRA) * Clinical Project Manager * Clinical Operations Manager * Data Manager * Biostatistician * Medical Monitor * Regulatory Affairs Specialist * Pharmacovigilance ...
Clinical Research Associate (CRA) * Clinical Project Manager * Clinical Operations Manager * Data Manager * Biostatistician * Medical Monitor * Regulatory Affairs Specialist * Pharmacovigilance ...
Clinical Research Associate (CRA) * Clinical Project Manager * Clinical Operations Manager * Data Manager * Biostatistician * Medical Monitor * Regulatory Affairs Specialist * Pharmacovigilance ...
Irvine, California, United States of America The Associate Director PMO, Clinical Programs, is accountable for enterprise integration and decision enablement across the clinical evidence portfolio.
Irvine, California, United States of America The Associate Director PMO, Clinical Programs, is accountable for enterprise integration and decision enablement across the clinical evidence portfolio.
Irvine, California, United States of America The Associate Director PMO, Clinical Programs, is accountable for enterprise integration and decision enablement across the clinical evidence portfolio.
Irvine, California, United States of America The Associate Director PMO, Clinical Programs, is accountable for enterprise integration and decision enablement across the clinical evidence portfolio.
Irvine, California, United States of America The Associate Director PMO, Clinical Programs, is accountable for enterprise integration and decision enablement across the clinical evidence portfolio.
Irvine, California, United States of America The Associate Director PMO, Clinical Programs, is accountable for enterprise integration and decision enablement across the clinical evidence portfolio.
Clinical Project Associate information
See California salary details
$12.57 - $16.39
3% of jobs
$16.39 - $20.21
18% of jobs
$20.96 is the 25th percentile. Wages below this are outliers.
$20.21 - $24.03
20% of jobs
The median wage is $26.34 / hr.
$24.03 - $27.84
15% of jobs
$27.84 - $31.66
11% of jobs
$31.66 - $35.48
4% of jobs
$38.72 is the 75th percentile. Wages above this are outliers.
$35.48 - $39.30
5% of jobs
$39.30 - $43.11
8% of jobs
$43.11 - $46.93
6% of jobs
$46.93 - $50.75
6% of jobs
$50.75 - $54.56
3% of jobs
$12
$31
$54
How much do clinical project associate jobs pay per hour?
What is a clinical project associate?
What are the typical responsibilities of a clinical project associate?
What are the key skills and qualifications needed to thrive as a clinical project associate?
What is the difference between Clinical Project Associate vs Clinical Research Coordinator?
| Aspect | Clinical Project Associate | Clinical Research Coordinator |
|---|---|---|
| Credentials | Bachelor's degree often required; certifications like CCRP beneficial | Bachelor's degree in health or related field; certifications like CCRP common |
| Work Environment | Typically works with project teams, sponsors, and CROs in clinical trial settings | Works directly with patients, investigators, and site staff at clinical trial sites |
| Employer & Industry | Pharmaceutical companies, CROs, biotech firms | Hospitals, clinics, research sites |
| Search & Comparison Intent | High overlap in responsibilities and certifications | Similar 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 are popular job titles related to Clinical Project Associate jobs in California?
For Clinical Project Associate jobs in California, the most frequently searched job titles 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:

Director, Clinical Research (Lingo)
Alameda, CA
Full-time
Medical, Retirement
Re-posted 28 days ago
Abbott rating
7.8
Based on 139 frontline employees who took The Breakroom Quiz
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 - $344,000.00In 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