Senior Principal Clinical Research Scientist
Location: Sylmar, CA (Cardiac Rhythm Management Division)
Company: Abbott
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 114,000 colleagues across 160+ countries, we are committed to advancing health and well-being worldwide.
Why Work at Abbott
At Abbott, you’ll have the opportunity to:
Do meaningful work that impacts lives.
Grow your career in an international company.
Care for yourself and your family with exceptional benefits.
Be your true self and thrive in an inclusive culture.
Employee Benefits include:
Free medical coverage under the Health Investment Plan (HIP) PPO (starting next calendar year).
Excellent retirement savings plan with high employer contribution.
Tuition reimbursement, Freedom 2 Save student debt program, and FreeU education benefit.
Recognition as a Great Place to Work in multiple countries and one of Fortune’s Most Admired Companies.
Named one of the best companies for diversity, working mothers, female executives, and scientists.
The Opportunity
Abbott’s Cardiac Rhythm Management division is a global leader in technologies for treating heart arrhythmias.
As a Senior Principal Clinical Research Scientist, you will:
Serve as a leader on clinical trial design, clinical evaluations, risk management, strategy, and data analysis.
Author and manage clinical evaluation plans/reports, trial protocols, risk master lists, trial registrations, results postings, timelines, and scientific publications.
Lead study support groups and cross-functional teams to develop clinical strategies.
Interact with regulatory agencies and provide scientific direction to internal teams and clinical study sites.
Mentor junior clinical scientists.
Key Responsibilities
Provide scientific leadership and strategic advice on clinical evaluations, trial design, risk management, and data analysis.
Collaborate with cross-functional teams (Biostatistics, RA, Clinical Operations, Data Management, Safety, R&D, Marketing, Quality, Product Performance, Risk Management, etc.).
Develop and deliver clinical evaluation plans/reports, study protocols, and scientific discussions.
Interpret and evaluate clinical/scientific/risk data and literature for product applications.
Present scientific results at industry meetings, investigator meetings, and regulatory discussions.
Support regulatory submissions and agency communications.
Participate in audits and ensure compliance with corporate/divisional policies and quality system requirements.
Manage financial, budgetary, and legal aspects as assigned.
Required Qualifications
Bachelor’s degree in a related field (or equivalent combination of education and experience).
Minimum 10 years of experience, including at least 5 years in clinical trials, risk management, or clinical evaluations.
Comprehensive knowledge of clinical research processes, risk management, and regulatory frameworks.
Recognized as an expert across functions with deep understanding of business unit operations and cross-functional dependencies.
Strong analytical, problem-solving, and decision-making skills.
Ability to exercise judgment within broadly defined practices and policies.
Compensation
Base Pay Range: $146,700 – $293,300 (range may vary by location).
How to Apply
Learn more about Abbott’s benefits: www.abbottbenefits.com
Explore career opportunities at: www.abbott.com
Connect with us:
Facebook: facebook.com/Abbott
Twitter: @AbbottNews | @AbbottGlobal
Abbott is an Equal Opportunity Employer, committed to diversity and inclusion.
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