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Clinical Data Specialist

6+ years
$83,500 – $153,300
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

 

Clinical Data Specialist – Abbott (Alameda, CA)

Job Summary:

Abbott, a global leader in diagnostics and medical devices, is seeking a Clinical Data Specialist to join its Clinical Research team in Alameda, California. This on-site role plays a pivotal part in ensuring the ethical conduct of clinical trials by monitoring data integrity, regulatory compliance, and participant safety. Ideal for professionals with 6+ years of clinical research or IVD data experience, this opportunity supports scientific excellence in clinical trial execution.


Key Responsibilities:

  • Assist with trial monitoring to ensure accuracy, reliability, and scientific validity of clinical data

  • Monitor adverse events and participant safety, ensuring early detection of risks

  • Review accumulating data to assess benefit-risk and make recommendations for study continuation or changes

  • Perform data cleaning and support final study report development

  • Monitor enrollment progress, protocol compliance, and data integrity across study sites

  • Support clinical research teams with internal audit preparation and compliance activities

  • Maintain clinical records, prepare study master file binders, and complete exception reports

  • Identify and support implementation of quality-enhancing processes and technologies

  • Contribute to development and maintenance of procedures, templates, and forms

  • Participate in training and cross-functional development activities


Required Skills & Qualifications:

  • Associate Degree required; Bachelor’s in Biological Science or Medical Specialty preferred

  • Minimum 6 years of experience in a clinical research environment or IVD laboratory

  • Strong knowledge of GCP regulations and standards for IVDs and Biologics

  • Experience with data analysis, clinical documentation systems (e.g., APLM, SBM), and contract support

  • Familiarity with electronic document management systems and internal compliance protocols

  • Ability to assess data consistency across multiple sites and studies


Perks & Benefits:

  • Competitive base salary: $83,500 – $153,300 (may vary by location)

  • Career development in a global healthcare organization

  • Comprehensive health benefits and quality-of-life support programs

  • Opportunities for cross-functional training and personal growth

  • Recognition as a top employer for diversity, inclusion, and scientific excellence


Company Description:

Abbott is a global healthcare company driving innovation across diagnostics, medical devices, nutrition, and branded generic medicines. With operations in over 160 countries, Abbott’s clinical research teams support life-changing advancements that improve global health outcomes. The Alameda, CA site focuses on cutting-edge IVD technologies and diabetes care solutions.


Work Mode:

On-site | Alameda, California | Monday to Friday


Call to Action:

Ready to contribute to safe and high-quality clinical trials with one of the world’s most trusted healthcare brands?
Apply now and make a meaningful impact at Abbott.