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Clinical Scientist Ii

5 years
$86,700.00 – $173,300.00
10 Sept. 9, 2025
Job Description
Job Type: Full Time Education: B.Sc/ M.Sc/ M.Pharm/ B.Pharm/ Life Sciences 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 Scientist II

Location: Alameda, CA
Division: Diabetes Care


About Abbott

Abbott is a global healthcare leader helping people live more fully at all stages of life. Our portfolio includes life-changing technologies in diagnostics, medical devices, nutritionals, and branded generic medicines. With 114,000 colleagues across more than 160 countries, we are committed to improving health worldwide.


Why Work at Abbott

At Abbott, you can do work that matters, grow professionally, and care for yourself and your family. Benefits include:

  • Career development opportunities with an international company.

  • Free medical coverage under our Health Investment Plan (HIP) PPO medical plan (from next calendar year).

  • Excellent retirement savings plan with high employer contributions.

  • Tuition reimbursement, Freedom 2 Save student debt program, and FreeU education benefit (affordable path to a bachelor’s degree).

  • Recognition as one of the World’s Most Admired Companies by Fortune.

  • Awarded as one of the best workplaces for diversity, working mothers, female executives, and scientists.


The Opportunity

As a Clinical Scientist II in our Diabetes Care division, you will contribute to advancing technologies that help people with diabetes manage their health. You’ll serve as a subject matter expert, strengthening Abbott’s scientific presence and supporting worldwide marketing strategies through clinical and technical expertise.


Key Responsibilities

  • Review Ad-Promo content for Clinical and Scientific Affairs.

  • Provide clinical/technical support to address product-related queries.

  • Generate literature summaries and technical write-ups for regulatory submissions.

  • Support writing and preparation of scientific papers and conference presentations.

  • Collaborate with cross-functional teams (Regulatory, R&D, Quality, Marketing, Medical Affairs).

  • Prepare and update technical documents for:

    • International regulatory submissions (IVDR Class C/D, novel products).

    • Domestic regulatory submissions (Class III, de novo).

  • Develop product and clinical labeling (vial/kit labels, instructions for use, clinical brochures).

  • Complete verification and stability records for high-risk products.

  • Create/update troubleshooting guides.

  • Coordinate documentation and submission activities across systems and stakeholders.

  • Proactively identify solutions, resolve issues, and lead cross-functional meetings.


Required Qualifications

  • Bachelor’s degree in science (biology, chemistry, microbiology, immunology, medical technology, pharmacy, pharmacology), math, engineering, or medical fields.

  • Equivalent combination of education and relevant experience will be considered.

  • Minimum 5 years’ experience in medical writing or a related field.


Compensation

  • Base pay range: $86,700 – $173,300 (may vary depending on location).


Apply Now

Be part of a company that is shaping the future of diabetes care and making a global impact.