Clinical Scientist II – Diabetes Care Division
📍 Location: Alameda, CA | Division: Diabetes Care
About Abbott
Abbott is a global healthcare leader helping people live more fully at all stages of life. With 114,000 colleagues across 160+ countries, our portfolio spans diagnostics, medical devices, nutritionals, and branded generic medicines.
Working at Abbott
At Abbott, you can:
Do work that truly matters.
Grow and develop your career with international opportunities.
Care for yourself and your family with comprehensive benefits.
Be your authentic self in an inclusive workplace.
Benefits Highlights:
Free medical coverage (HIP PPO plan – eligibility starting next calendar year).
Excellent retirement savings plan with high employer contributions.
Tuition reimbursement, Freedom 2 Save (student debt program), and FreeU education benefits.
Recognized globally as a Great Place to Work, Most Admired Company (Fortune), and Top Employer for Diversity, Working Mothers, Female Executives, and Scientists.
The Opportunity
This role is part of Abbott’s Diabetes Care Division, focused on developing innovative technologies that help people with diabetes manage their health. Our revolutionary glucose sensing technology is changing the way people monitor and understand their condition.
As a Clinical Scientist II, you will serve as a subject matter expert to strengthen Abbott’s scientific presence, support marketing strategies worldwide, and provide clinical and technical expertise to ensure product claims are appropriately substantiated.
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 the writing of papers and presentations for peer-reviewed journals and conferences.
Collaborate with cross-functional stakeholders (Regulatory, R&D, Quality, Marketing, Medical Affairs).
Create/update technical documents for medium-risk domestic and international regulatory submissions (e.g., IVDR Class C/D, US Class III, de novo).
Prepare product and clinical labeling (vials, kits, IFUs, brochures) for high-risk/visibility products.
Complete verification and stability records for high-risk/visibility products.
Develop and maintain troubleshooting guides.
Independently coordinate activities, schedule and lead team meetings, and resolve issues.
Propose and refine templates, tools, and best practices for assigned tasks.
Required Qualifications
Bachelor’s degree in Science (Biology, Chemistry, Microbiology, Immunology, Medical Technology, Pharmacy, Pharmacology), Math, Engineering, or related medical fields.
Equivalent combination of education and experience considered in lieu of degree.
Minimum 5 years of experience in Medical Writing or related field.
Compensation
💰 Base Pay Range: $86,700 – $173,300 (Location-based variations may apply).
Apply Now
👉 Learn more about Abbott’s benefits: www.abbottbenefits.com
👉 Explore Abbott careers: www.abbott.com
Connect with us:
Facebook: facebook.com/Abbott
Twitter: @AbbottNews
📢 Abbott is an Equal Opportunity Employer committed to diversity and inclusion.
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