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Associate I Clinical Research

2+ years
$72,100 – $114,700
10 May 5, 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: Associate I, Clinical Research

Company: Abbott
Location: Alameda, California, United States
Department: Abbott Diabetes Care Division (ADCD)


Company Overview

Abbott is a global healthcare leader offering innovative technologies across diagnostics, medical devices, nutrition, and branded generic medicines. With over 114,000 employees in more than 160 countries, Abbott is recognized globally for workplace excellence, diversity, and career development opportunities.


Role Summary

The Associate I, Clinical Research (CRA) supports the full lifecycle of clinical trials focused on diabetes care. The position ensures quality and regulatory compliance (FDA, ICH-GCP, ISO14155) and is onsite at the Alameda, CA office. This is not a remote role.


Key Responsibilities

  • Perform site visits (SQV, SIV, IMV, COV), generate monitoring reports, and track resolution of action items

  • Ensure compliance with protocols, GCP, ICH, ISO14155, and regulatory standards

  • Participate in study start-up activities and assist in shipment of devices/supplies

  • Maintain and reconcile study device accountability

  • Contribute to CRF design, monitoring plans, and site training

  • Upload and audit Trial Master File (TMF/eTMF) for inspection readiness

  • Review data listings and escalate issues to study leads as necessary

  • Participate in data reviews for regulatory submissions and respond to audits

  • Travel 30–50% as required for site visits and monitoring


Qualifications

  • Education: BS in life sciences (preferred) or equivalent experience

  • Experience:

    • Minimum 2 years of clinical research experience

    • Background in medical device or in-vitro diagnostics (preferred); pharmaceutical experience considered

  • Skills:

    • Excellent interpersonal and team collaboration skills

    • Knowledge of CFR, ICH-GCP, and clinical regulatory practices

    • Proficient in Microsoft Office


Compensation & Benefits

  • Base Salary: $72,100 – $114,700 (may vary by location)

  • Benefits:

    • Free medical coverage for eligible employees under the HIP PPO plan

    • 401(k) with generous employer match

    • Tuition reimbursement & student debt support (Freedom 2 Save, FreeU)

    • Paid time off and comprehensive health & wellness programs

    • Recognized training and career development opportunities


Additional Info

  • Recognized as one of the best workplaces globally for diversity, women, working mothers, and scientists

  • Visit: www.abbott.com | Benefits Info