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Clinical Data Specialist

3+ years
$86,700 – $173,300
10 July 4, 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

 

Clinical Data Specialist – Abbott | Alameda, California

Job Summary:

Abbott is seeking a skilled Clinical Data Specialist to join its Clinical Research team in Alameda, CA. This position supports clinical operations and ensures data quality and regulatory compliance across investigational studies. If you have a background in clinical research, IVD instruments, and GCP compliance, this is your opportunity to work with one of the world’s leading healthcare companies.


Key Responsibilities:

  • Support clinical operations per Good Clinical Practice (GCP) and regulatory standards.

  • Facilitate execution and tracking of Clinical Research Agreements (CRAs) and amendments.

  • Coordinate payments, clinical supplies, and instrument shipping for clinical sites.

  • Maintain documentation for financial disclosures, denied party screening, and Sunshine Act tracking.

  • Provide operational support to Clinical Research Associates (CRAs), including study master files, routing documents, and data exception reports.

  • Assist with internal audits, OEC reviews, and QA verification of clinical data.

  • Monitor clinical study data and support data quality improvements.

  • Identify and lead process improvement initiatives.

  • Develop and maintain SOPs, templates, and clinical procedures using APLM systems.

  • Ensure compliance and timely execution of assigned clinical activities.


Required Skills & Qualifications:

  • Associate’s Degree (minimum); Bachelor’s in Biological Science or Medical Specialty preferred.

  • 3+ years of experience in a clinical research or laboratory environment.

  • Knowledge of IVD assays/instruments and data analysis.

  • Understanding of clinical trial regulations and GCP standards.

  • Experience working with clinical contracts and electronic document management systems (e.g., APLM, SBM).

  • Excellent communication and organizational skills.


Perks & Benefits:

  • Base salary range: $86,700 – $173,300 (location dependent)

  • Free medical coverage with HIP PPO upon wellness participation

  • 401(k) plan with high employer contributions

  • Tuition reimbursement and education support through FreeU

  • Career advancement in a globally recognized company

  • Inclusive workplace and diversity programs

  • Wellness programs and access to world-class health benefits


Company Description:

Abbott is a global healthcare leader in medical devices, diagnostics, nutrition, and branded generics. With over 114,000 employees in 160+ countries, Abbott pioneers life-changing technologies that improve health at every stage of life—especially in clinical research, IVD development, and data-driven innovation.


Work Mode:

On-site – Alameda, California, United States


Call to Action:

Are you ready to elevate your career in clinical data management and work on cutting-edge diagnostic innovations? Apply now for the Clinical Data Specialist role at Abbott and help shape the future of healthcare.