Instagram
youtube
Facebook

Clinical Research Associate I

1+ years
$72,100.00 – $114,700.00 annually
10 July 29, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Job Title: Clinical Research Associate I

Location: Alameda, California, United States
Company: Abbott
Work Mode: On-site
Compensation:$72,100.00 – $114,700.00 annually


Job Summary

Abbott, a global leader in healthcare innovation, is seeking a Clinical Research Associate I to join its Medical and Clinical Affairs team in Alameda, California. This role focuses on the integrity, compliance, and accuracy of clinical trial data, involving direct interaction with study sites and internal stakeholders. Ideal for professionals in clinical trial monitoring, medical device research, and regulatory affairs.


Key Responsibilities

  • Conduct study site visits (SQV, SIV, IMV, COV) and track resolution of site-related issues

  • Perform clinical monitoring and site management according to protocols and GCP guidelines

  • Support study start-up activities including site training and shipping of study devices

  • Manage study device accountability and reconciliation

  • Maintain and audit Trial Master File (TMF) and ensure accurate eTMF uploads

  • Assist with CRF design, monitoring plans, and regulatory documentation

  • Review clinical data for completeness and escalate issues to Clinical Operations Manager

  • Support interim and final study data review for regulatory submissions

  • Participate in audits and FDA inspections as needed

  • Travel up to 30–50%, or more depending on project needs


Required Skills & Qualifications

  • Bachelor’s degree in Life Sciences or equivalent; clinical research experience required

  • Minimum 1 year of experience in clinical research (medical device or pharma preferred)

  • Familiarity with ICH-GCP, CFR, ISO14155, and clinical trial regulations

  • Experience with in-vitro diagnostics or medical device studies preferred

  • Proficiency in Microsoft Office (Word, Excel, Outlook)

  • Strong communication, organizational, and interpersonal skills

  • Ability to travel extensively as needed


Perks & Benefits

  • Competitive salary: $72,100 – $114,700

  • Work with a global healthcare leader

  • Exposure to cutting-edge clinical research and regulatory frameworks

  • Comprehensive training and mentorship from senior staff

  • Professional growth and development opportunities


About Abbott

Abbott is a global healthcare company serving people in more than 160 countries. With a portfolio that spans diagnostics, medical devices, nutrition, and branded generic medicines, Abbott is committed to advancing health at all stages of life. Known for innovation and quality, Abbott is a leader in clinical and regulatory excellence.


Work Mode

On-site – Alameda, California


Call to Action

Ready to advance your clinical research career with a global healthcare leader? Apply now to join Abbott as a Clinical Research Associate I and contribute to impactful clinical studies that shape the future of healthcare.