Clinical Affairs Manager – Lingo Division (Alameda, CA)
Company: Abbott
Location: Alameda, California (Lingo Division)
Job Type: Full-time
About Abbott
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans diagnostics, medical devices, nutritionals, and branded generic medicines. With over 114,000 colleagues across more than 160 countries, Abbott is recognized as one of the world’s most admired companies by Fortune.
Working at Abbott
At Abbott, you can do meaningful work, grow your career, and care for yourself and your family. We are committed to creating an inclusive and rewarding workplace.
Employee Benefits:
Career Development: Opportunities to grow globally and achieve your career goals.
Medical Coverage: Employees may qualify for free medical coverage under our Health Investment Plan (HIP) PPO.
Retirement Savings: Excellent plan with high employer contributions.
Education Assistance: Tuition reimbursement, Freedom 2 Save student debt program, and FreeU education benefit for affordable bachelor’s degrees.
Recognition: Consistently ranked among the best companies to work for diversity, women, mothers, executives, and scientists.
The Opportunity – Lingo Division
Lingo is Abbott’s next-generation technology that empowers individuals to make informed lifestyle decisions—whether improving energy, losing weight, or enhancing athletic performance.
As a Clinical Affairs Manager, you will manage teams within the Medical Affairs Sub-Function, focusing on policy and strategy implementation and short-term operational/tactical responsibilities.
Key Responsibilities
Lead strategy implementation and operations for clinical trials/research and data collection.
Contribute to clinical protocol development and oversee completion of final reports.
Recruit and negotiate with clinical investigators regarding study design and costs.
Direct human clinical trials for products under development.
Monitor safety and participate in adverse event reporting.
Prepare reports for submission to regulatory agencies.
Ensure adherence to protocols and oversee study completion.
Coordinate investigator initiations and group studies.
Act as a consultant/liaison with external partners under licensing agreements.
Required Qualifications
Bachelor’s degree
Minimum 8 years of relevant experience
Preferred Qualifications
Master’s or PhD in science or related field
Strong background in clinical operations
Experience in:
Quality management system (QMS) gap analysis & audit preparation
Corrective and Preventive Actions (CAPA)
Digital consumer behavior understanding
Software life cycle processes
Compensation
Base Pay Range: $112,000 – $224,000 (may vary based on location)
How to Apply
Apply directly via: Abbott Careers
Connect with us:
Website: www.abbott.com
Facebook: facebook.com/Abbott
Twitter: @AbbottNews
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