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Clinical Research Associate I

Abbott

Clinical Research Associate I

full-timePosted: Jan 12, 2026

Job Description

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.
  • Free medical coverage for employees* via the Health Investment Plan (HIP) PPO
  • 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

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 GCP, and ISO14155. This position is onsite in our Alameda, CA location.

What you’ll work on

  • Perform study site visits (SQV, SIV, IMV, COV), generate monitoring reports, and track resolution of action items.  
  • Assist and conduct clinical monitoring and site management activities, ensuring compliance to the Study Protocol, Good Clinical Practices (GCPs), ICH guidelines, Federal Regulations, department procedures, and other applicable regulatory requirements.
  • Participate in study start up activities.
  • Assist with shipping study devices and supplies to clinical sites.
  • Perform study device accountability and reconciliation.
  • Assist senior staff in development of study-specific forms and trial-specific monitoring plans.
  • Assist senior staff in study planning, designing case report forms (CRFs), and training of study sites.
  • Maintain and audit Trial Master File (TMF) and upload to eTMF to ensure inspection readiness.
  • 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 status of clinical studies to management.
  • Participate in the interim and final reviews of study data in preparation of regulatory submissions.
  • May interact with RA/QA in responding to audits and FDA inquiries.
  • Perform any other duties as assigned by management.
  • Must be able to travel 30-50%-, with additional travel as required.

Required Qualifications

  • BS degree in life sciences preferred or equivalent with minimum one (1)  year of clinical research experience, or combination of appropriate education and experience.
  • Experience working on medical device studies and/or in-vitro diagnostics studies preferred. Pharmaceutical background may also be considered.
  • Perform any other duties as assigned by management.
  • Demonstrate excellence in teamwork, solid interpersonal and communication skills including building rapport with team members/peers, study site staff, and clinical management.
  • Working knowledge of CFR, ICH-GCP, Clinical and Regulatory Affairs
  • Proficient with Microsoft Suite

What We Offer

At Abbott, you can have a good job that can grow into a great career. We offer: 

  • Training and career development, with onboarding programs for new employees and tuition assistance  
  • Financial security through competitive compensation, incentives and retirement plans  
  • Health care and well-being programs including medical, dental, vision, wellness and occupational health programs 
  • Paid time off  
  • 401(k) retirement savings with a generous company match 
  • The stability of a company with a record of strong financial performance and history of being actively involved in local communities 

Learn more about our benefits that add real value to your life to help you live fully:  www.abbottbenefits.com  

Follow your career aspirations to Abbott for diverse opportunities with a company that provides the growth and strength to build your future. 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 $73,900.00 – $116,000.00. In specific locations, the pay range may vary from the range posted.

Locations

  • Alameda, California, United States

Salary

Estimated Salary Rangemedium confidence

55,000 - 95,000 USD / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Clinical monitoringintermediate
  • Site managementintermediate
  • Study site visits (SQV, SIV, IMV, COV)intermediate
  • Trial Master File (TMF) maintenanceintermediate
  • Data review and auditingintermediate
  • Regulatory compliance (CFR, ICH GCP, ISO14155)intermediate

Required Qualifications

  • BS degree in life sciences preferred (experience)
  • Minimum 1 year clinical research experience (experience)
  • Experience in medical device or in-vitro diagnostics studies preferred (experience)

Responsibilities

  • Perform study site visits and generate monitoring reports
  • Assist in clinical monitoring and site management
  • Participate in study start-up activities
  • Assist with shipping study devices and supplies
  • Perform study device accountability and reconciliation
  • Maintain and audit TMF
  • Review clinical data listings
  • Communicate study status to management
  • Participate in data reviews for regulatory submissions
  • Travel 30-50%

Benefits

  • general: Free medical coverage via Health Investment Plan (HIP) PPO
  • general: Excellent retirement savings plan with high employer contribution
  • general: Tuition reimbursement
  • general: Freedom 2 Save student debt program
  • general: FreeU education benefit

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Abbott logo

Clinical Research Associate I

Abbott

Clinical Research Associate I

full-timePosted: Jan 12, 2026

Job Description

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.
  • Free medical coverage for employees* via the Health Investment Plan (HIP) PPO
  • 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

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 GCP, and ISO14155. This position is onsite in our Alameda, CA location.

What you’ll work on

  • Perform study site visits (SQV, SIV, IMV, COV), generate monitoring reports, and track resolution of action items.  
  • Assist and conduct clinical monitoring and site management activities, ensuring compliance to the Study Protocol, Good Clinical Practices (GCPs), ICH guidelines, Federal Regulations, department procedures, and other applicable regulatory requirements.
  • Participate in study start up activities.
  • Assist with shipping study devices and supplies to clinical sites.
  • Perform study device accountability and reconciliation.
  • Assist senior staff in development of study-specific forms and trial-specific monitoring plans.
  • Assist senior staff in study planning, designing case report forms (CRFs), and training of study sites.
  • Maintain and audit Trial Master File (TMF) and upload to eTMF to ensure inspection readiness.
  • 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 status of clinical studies to management.
  • Participate in the interim and final reviews of study data in preparation of regulatory submissions.
  • May interact with RA/QA in responding to audits and FDA inquiries.
  • Perform any other duties as assigned by management.
  • Must be able to travel 30-50%-, with additional travel as required.

Required Qualifications

  • BS degree in life sciences preferred or equivalent with minimum one (1)  year of clinical research experience, or combination of appropriate education and experience.
  • Experience working on medical device studies and/or in-vitro diagnostics studies preferred. Pharmaceutical background may also be considered.
  • Perform any other duties as assigned by management.
  • Demonstrate excellence in teamwork, solid interpersonal and communication skills including building rapport with team members/peers, study site staff, and clinical management.
  • Working knowledge of CFR, ICH-GCP, Clinical and Regulatory Affairs
  • Proficient with Microsoft Suite

What We Offer

At Abbott, you can have a good job that can grow into a great career. We offer: 

  • Training and career development, with onboarding programs for new employees and tuition assistance  
  • Financial security through competitive compensation, incentives and retirement plans  
  • Health care and well-being programs including medical, dental, vision, wellness and occupational health programs 
  • Paid time off  
  • 401(k) retirement savings with a generous company match 
  • The stability of a company with a record of strong financial performance and history of being actively involved in local communities 

Learn more about our benefits that add real value to your life to help you live fully:  www.abbottbenefits.com  

Follow your career aspirations to Abbott for diverse opportunities with a company that provides the growth and strength to build your future. 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 $73,900.00 – $116,000.00. In specific locations, the pay range may vary from the range posted.

Locations

  • Alameda, California, United States

Salary

Estimated Salary Rangemedium confidence

55,000 - 95,000 USD / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Clinical monitoringintermediate
  • Site managementintermediate
  • Study site visits (SQV, SIV, IMV, COV)intermediate
  • Trial Master File (TMF) maintenanceintermediate
  • Data review and auditingintermediate
  • Regulatory compliance (CFR, ICH GCP, ISO14155)intermediate

Required Qualifications

  • BS degree in life sciences preferred (experience)
  • Minimum 1 year clinical research experience (experience)
  • Experience in medical device or in-vitro diagnostics studies preferred (experience)

Responsibilities

  • Perform study site visits and generate monitoring reports
  • Assist in clinical monitoring and site management
  • Participate in study start-up activities
  • Assist with shipping study devices and supplies
  • Perform study device accountability and reconciliation
  • Maintain and audit TMF
  • Review clinical data listings
  • Communicate study status to management
  • Participate in data reviews for regulatory submissions
  • Travel 30-50%

Benefits

  • general: Free medical coverage via Health Investment Plan (HIP) PPO
  • general: Excellent retirement savings plan with high employer contribution
  • general: Tuition reimbursement
  • general: Freedom 2 Save student debt program
  • general: FreeU education benefit

Target Your Resume for "Clinical Research Associate I" , Abbott

Get personalized recommendations to optimize your resume specifically for Clinical Research Associate I. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Clinical Research Associate I" , Abbott

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score
Quiz Challenge

Answer 10 quick questions to check your fit for Clinical Research Associate I @ Abbott.

10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.