🧬 Job Title: Principal Clinical Scientist
Category: Medical and Clinical Affairs
Organization: Abbott Laboratories
Division: Structural Heart (SH) Division
Locations: Multiple (See All)
🌍 About Abbott
Abbott is a global healthcare leader that helps people live more fully at all stages of life. The company’s portfolio spans:
Diagnostics
Medical Devices
Nutritionals
Branded Generic Medicines
With 114,000+ employees across 160+ countries, Abbott is consistently recognized as a top employer and one of the “World’s Most Admired Companies” by Fortune.
💼 Working at Abbott – Key Benefits
Career Development: Opportunities for global growth and professional learning.
Health Coverage: Employees can qualify for free medical coverage under the Health Investment Plan (HIP) PPO.
Retirement Plan: Excellent savings plan with high employer contribution.
Education Support:
Tuition reimbursement
Freedom 2 Save student debt program
FreeU education benefit (affordable path to a bachelor’s degree)
Recognition:
One of the Best Big Companies to Work For
Recognized for diversity, working mothers, female executives, and scientists
🫀 Division Mission: Structural Heart
Business Purpose:
To restore health and improve quality of life by designing and providing device and management solutions for treating structural heart diseases.
🎯 Role Overview
As a Principal Clinical Scientist, you will:
Collaborate closely with cross-functional clinical study teams (including project management, biostatistics, data management, and regulatory affairs).
Interact with senior leadership and regulatory authorities.
Execute all responsibilities within Abbott’s corporate policies and standard operating procedures (SOPs).
🧠 Key Responsibilities
1. Clinical Strategy & Documentation
Develop or mentor creation of clinical strategies, risk management, and evaluation plans for product and process changes.
Prepare or guide the preparation of essential study-related documents:
Clinical study reports
Study protocols
Case Report Forms (CRFs)
Investigator Brochures
Informed Consent Forms (ICFs)
2. Clinical Trial Design
Design and mentor the design of clinical trials in collaboration with internal and external stakeholders.
Provide scientific justification and protocol development support.
Conduct pre-protocol analysis and contribute to scientific rationale documentation.
3. Publications & Communication
Develop and execute scientific publication strategies and coordinate with investigators and internal teams.
Lead podium presentations and publication efforts.
4. Regulatory & Statistical Oversight
Review and critically analyze Statistical Analysis Plans (SAPs).
Prepare documents for regulatory submissions and respond to authority queries.
🎓 Required Qualifications
Education: Advanced degree (M.Sc., M.Pharm., MD, or equivalent) in a scientific, medical, or related discipline.
Experience: 8+ years of relevant experience with strong domain knowledge.
Skills:
Proven scientific writing ability
Strong analytical and decision-making skills
Experience working in a quality system environment
🌟 Preferred Qualifications
PhD in a relevant scientific or medical discipline
Experience in regulated and post-market clinical studies
Knowledge of MDR requirements, and experience creating PMCF Plans/Reports
Experience with medical device clinical trials
Familiarity with quality system environments
Prior collaboration with external research committees (e.g., DSMB, CEC, screening committees)
Experience in physician and safety management
💰 Compensation
Base Pay Range:
💵 $97,300 – $194,700 (may vary by location)
🔗 How to Apply
👉 Learn more about Abbott’s benefits: www.abbottbenefits.com
👉 Apply and connect at: www.abbott.com
👉 Follow Abbott:
Facebook: facebook.com/Abbott
Twitter: @AbbottNews
🤝 Equal Opportunity Statement
Abbott is an Equal Opportunity Employer, committed to diversity and inclusion across all levels of employment.
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