Senior Clinical Research Scientist

Abbott • Los Angeles, CA

2d • $90,000 - $180,000 • Onsite

About The Position

At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to: Career development with an international company where you can grow the career you dream of Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year. An excellent retirement savings plan with high employer contribution Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists For years, Abbott’s medical device businesses have offered technologies that are faster, more effective, and less invasive. Whether it’s glucose monitoring system, innovative therapies for treating heart disease, or products that help people with chronic pain or movement disorders, our medical device technologies are designed to help people live their lives better and healthier. Every day, our technologies help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine fingersticks. The Opportunity Our location in Sylmar, CA currently has an on-site opportunity for a Senior Clinical Research Scientist. This new team member will work in Abbott’s Global Data Science & Analytics team within the Medical Device Division. The Senior Clinical Research Scientist will provide scientific and technical leadership for real‑world evidence (RWE) studies supporting post‑market regulatory requirements, reimbursement, clinical evidence generations, and pre-market submissions across Abbott’s Electrophysiology portfolio. This individual will lead the design, execution, and dissemination of observational studies using large‑scale real‑world data sources, including electronic health records (EHR), insurance claims, hospital administrative and billing databases, and device‑generated data.

Requirements

• Associates Degree
• 4 years related experience

Nice To Haves

• Master's Degree with 4+ years of related experience OR Bachelor's Degree with 6-8 years of related experience OR an equivalent combination of education and work experience.
• PhD, DrPH, PharmD, MS, or equivalent advanced degree in biostatistics, epidemiology, clinical research, public health, outcomes research, biomedical engineering, or a related field.
• 2-5+ years’ Experience leading real‑world evidence, observational research, or outcomes research studies in the medical device, pharmaceutical, or life sciences industry, with increasing levels of scientific responsibility.
• Experience designing and executing regulatory‑grade clinical studies or RWE studies.
• Strong expertise working with large real‑world datasets, including electronic health records, administrative claims data, hospital billing/chargemaster data, registries, and/or device‑generated data.
• Advanced hands‑on experience in statistical programming and data analysis using one or more of the following: SQL, R, SAS, Python (or equivalent), with the ability to independently execute complex cohort‑based analyses.
• Deep understanding of epidemiologic study design and analytical methods for observational research, including cohort studies, comparative effectiveness research, signal detection, sensitivity analyses, and bias mitigation strategies.
• Proven ability to develop RWE protocols and statistical analysis plans suitable for regulatory review, including clear articulation of study objectives, endpoints, data sources, and analytical approaches.
• Familiarity with regulatory and methodological guidance relevant to real‑world evidence, including FDA expectations for data relevance, reliability, and transparency.
• Prior experience leading the development of study reports, regulatory submissions, peer‑reviewed manuscripts, conference abstracts, and scientific presentations.
• Background or strong working knowledge of the cardiac electrophysiology therapeutic area, including atrial fibrillation, atrial flutter, ventricular arrhythmias, catheter ablation technologies, and evolving standards of care, with the ability to interpret results in a clinically meaningful context.
• Demonstrated ability to stay current with the clinical and competitive landscape in electrophysiology, including emerging technologies, clinical guidelines, and real‑world evidence trends.
• Experience collaborating effectively with cross‑functional teams (e.g., clinical affairs, regulatory affairs, medical affairs, health economics, data science, biostatistics) and influencing without formal authority.
• Demonstrated ability to manage multiple complex projects simultaneously, prioritize effectively, and deliver high‑quality scientific work under tight timelines, with strong attention to detail and commitment to analytical rigor.
• Strong scientific communication skills, with the ability to translate complex analyses into clear, actionable insights for diverse audiences, including clinicians, regulators, and internal leadership.
• Experience working with external collaborators such as academic investigators, data vendors, or health system partners is preferred.

Responsibilities

• Lead the design and execution of real‑world evidence, health economics, and digital health studies related to Abbott medical devices, using real‑world data sources such as electronic health records, insurance claims, and hospital administrative/billing databases.
• Develop and own RWE study protocols and statistical analysis plans (SAPs) aligned with regulatory, clinical, and reimbursement objectives.
• Build and help execute long‑term RWE generation strategies across the electrophysiology portfolio, in collaboration with clinical, regulatory, medical affairs, and market access stakeholders.
• Perform hands‑on programming to execute RWE studies using SQL, R, SAS, Python, or similar languages.
• Manage data preparation, cohort construction, variable derivation, and analysis across diverse data types, including EHR data, insurance claims, hospital billing data, device‑generated data, and clinical trial data.
• Partner closely with data analysts and data engineers to validate programming logic, analytical datasets, and study results, ensuring accuracy, reproducibility, and regulatory readiness.
• Lead development of study reports, regulatory deliverables, conference abstracts, podium and poster presentations, and peer‑reviewed scientific manuscripts.
• Translate complex analytical results into clear, clinically meaningful scientific narratives for internal leadership, regulators, clinicians, and external stakeholders.
• Maintain strong and up‑to‑date knowledge of the clinical landscape in cardiac electrophysiology, including atrial fibrillation, atrial flutter, ventricular arrhythmias, ablation technologies, and evolving standards of care.
• Monitor emerging evidence, clinical guidelines, competitive technologies, and unmet clinical needs to inform RWE study design, endpoint selection, and evidence generation strategy.
• Apply clinical context to interpret real‑world data results, assess relevance to intended use populations, and support regulatory and clinical decision‑making.
• Collaborate effectively with peers across biostatistics, clinical affairs, regulatory affairs, medical affairs, health economics, and R&D teams.
• Represent RWE and observational research perspectives in cross‑functional project teams and strategy discussions.
• Engage with external collaborators, including academic researchers, data vendors, and clinical experts, as appropriate.

Benefits

• Career development with an international company where you can grow the career you dream of
• Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
• An excellent retirement savings plan with high employer contribution
• Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree
• A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune
• A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Associate degree
• Number of Employees: 5,001-10,000 employees