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Principal Clinical Research Scientist – Electrophysiology Division

5 years
$97,300 – $194,700
10 Nov. 21, 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 Research Scientist – Electrophysiology Division

Locations: St. Paul, MN | Plymouth, MN | Austin, TX | Santa Clara, CA
Category: Medical and Clinical Affairs


About Abbott

Abbott is a global healthcare leader advancing medical science to improve patient outcomes and quality of life. Our Electrophysiology (EP) business is at the forefront of heart disease treatment, offering breakthrough medical devices and therapies for atrial fibrillation and related cardiac conditions. With over 114,000 colleagues in 160+ countries, Abbott combines innovation, expertise, and patient-centric solutions to transform healthcare globally.


Position Overview

Abbott is seeking a Principal Clinical Research Scientist to lead clinical research activities within the Electrophysiology (EP) division. This senior scientific role involves designing, conducting, and reporting clinical trials, generating evidence to support regulatory approvals, reimbursement, and global commercial adoption of medical devices. The position will collaborate with cross-functional teams, regulatory authorities, and physician Key Opinion Leaders (KOLs) to drive scientific excellence and clinical innovation.

This role is available in St. Paul, MN; Plymouth, MN; Austin, TX; and Santa Clara, CA and requires interaction with both domestic and international study sites and regulatory agencies.


Key Responsibilities

  • Lead and mentor teams in clinical trial design, protocol development, and publication planning.

  • Develop, review, and approve clinical study documents, including protocols, case report forms (CRFs), clinical study reports (CSRs), informed consent forms, and investigator brochures.

  • Critically analyze statistical analysis plans and interpret study data.

  • Support regulatory submissions and ongoing compliance with international medical device regulations.

  • Collaborate with cross-functional teams including Marketing, R&D, Program Management, Reimbursement, Medical Affairs, Risk Management, Quality, and Regulatory Affairs.

  • Oversee study Steering Committees and Publication Committees with global physician KOLs.

  • Present clinical trial results to senior leadership, investigator meetings, and external scientific audiences.

  • Participate in audits and ensure adherence to Quality System standards and Good Clinical Practices (GCP).

  • Drive innovative solutions and work independently on complex scientific and clinical challenges.


Required Qualifications

  • Advanced degree in sciences, medicine, or related discipline.

  • Minimum 5+ years of clinical research experience post-degree, preferably in medical devices or electrophysiology.

  • Strong scientific writing and communication skills for protocols, reports, and publications.

  • Experience with international regulatory submissions and compliance requirements for medical devices.

  • Proven ability to manage complex projects and collaborate effectively with cross-functional teams.

  • Strong organizational skills, attention to detail, and the ability to prioritize in a fast-paced environment.


Preferred Qualifications

  • PhD in sciences, medicine, or related discipline.

  • Experience in the medical device industry and electrophysiology clinical trials.

  • Familiarity with international regulatory requirements, quality systems, and clinical investigations.

  • Experience mentoring junior scientific staff and leading clinical research teams.


Compensation

Base Pay: $97,300 – $194,700 (may vary by location and experience)


Why Join Abbott

  • Opportunity to lead clinical research for innovative heart disease therapies.

  • Access to global career development and learning programs.

  • Comprehensive health, wellness, and retirement benefits.

  • Support for tuition reimbursement and educational advancement.

  • Work in a diverse, inclusive, and globally recognized organization.

Learn more about Abbott benefits at www.abbottbenefits.com.

Abbott is an Equal Opportunity Employer, committed to fostering diversity, equity, and inclusion in the workplace.


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