Instagram
youtube
Facebook

Principal Clinical Scientist

8+ years
Not Disclosed
10 Nov. 19, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Principal Clinical Scientist

Locations Available: Santa Clara (CA), Temecula (CA), St. Paul (MN), Westford (MA)
Category: Medical and Clinical Affairs
Work Model: Onsite (Daily Onsite Presence Required)

About Abbott

Abbott is a global healthcare leader dedicated to advancing health through innovative diagnostics, medical devices, nutrition solutions, and branded generic medicines. With more than 114,000 employees across 160+ countries, Abbott delivers technologies that support healthier lives at every stage.


Role Overview

The Principal Clinical Scientist is a senior-level scientific leadership role within Abbott’s Vascular Division. This position is responsible for designing, executing, and directing clinical studies supporting regulatory submissions and strategic business needs. The role requires strong scientific expertise, cross-functional leadership, and the ability to drive clinical evidence generation for vascular medical devices.

This is a full-time onsite position at one of the listed Abbott Vascular locations.


Key Responsibilities

Clinical Study Design & Strategy

  • Design clinical trials and studies in collaboration with cross-functional teams including clinical operations, biostatistics, data management, medical affairs, and regulatory affairs

  • Support clinical strategies aligned with premarket approval (PMA), 510(k) submissions, and broader business objectives

  • Provide scientific and technical guidance to internal and external stakeholders, including steering committees, investigators, and regulatory partners

Scientific Leadership

  • Serve as Clinical Science Lead on study teams, providing justification for trial design and ongoing scientific analysis

  • Support generation of pre-protocol documentation and pre-submissions to regulatory authorities

  • Lead or contribute to clinical protocols, case report forms, study reports, informed consent forms, and related documentation

Data Analysis & Communication

  • Critically evaluate clinical data and present findings to clinicians, leadership teams, and regulatory bodies

  • Lead podium strategy, abstract submissions, manuscripts, and publications in collaboration with investigators and internal teams

  • Synthesize scientific literature and competitive intelligence across therapeutic areas

Regulatory Support

  • Prepare scientific documents for regulatory submissions and respond to queries from global regulatory authorities

  • Lead and present at FDA or other regulatory meetings

  • Ensure adherence to quality system requirements and regulatory guidelines

Process Improvement & Mentorship

  • Identify opportunities to optimize clinical processes and internal workflows

  • Support innovation initiatives with new ideas and scientific perspectives

  • Mentor and guide junior clinical science team members


Required Qualifications

  • Bachelor’s degree required; advanced degree (MS, PhD, MD, PharmD) strongly preferred

  • Minimum 8+ years of relevant experience in clinical research, medical device development, or a scientific/technical discipline

  • Strong expertise in a relevant technological field, preferably cardiovascular or vascular devices

  • Proven ability to work on complex problems requiring advanced scientific judgment

  • Experience operating in a regulated environment (FDA, ISO standards, quality systems)

  • Demonstrated leadership in cross-functional scientific teams


Preferred Qualifications

  • Proficiency in MS Office Suite

  • Experience in the medical device industry

  • Clinical trial design and execution experience

  • Background in vascular or cardiovascular therapeutic areas


Compensation

Base Salary Range: 112,000 USD – 224,000 USD
Actual compensation may vary based on location and candidate seniority. Hiring typically aligns with the midpoint of the range.


Why Join Abbott

  • Comprehensive career development with a globally recognized healthcare leader

  • Free medical coverage eligibility for employees through Abbott’s HIP PPO plan

  • Competitive retirement savings plan with high employer contribution

  • Tuition assistance, student debt support programs, and FreeU bachelor’s degree pathway

  • Recognized as one of the world’s most admired and inclusive employers


Apply Now

Interested candidates can apply through Abbott’s official career portal.

Abbott is an Equal Opportunity Employer committed to building a diverse and inclusive workforce.