Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Clinical Fellow

Abbott
Abbott
12+ years
$172,000.00 – $344,000.00
10 Jan. 6, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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

Clinical Fellow – Cardiac Rhythm Technologies

Location: Sylmar, California, USA
Category: Medical & Clinical Affairs
Employment Type: Full-time


Company Overview

Abbott is a global healthcare leader dedicated to improving lives at all stages through innovative diagnostics, medical devices, nutritionals, and branded generics. Abbott’s Cardiac Rhythm Technologies division develops next-generation solutions to treat patients with heart arrhythmias and irregular heartbeats.


Role Overview

Abbott is seeking a Clinical Fellow to provide clinical expertise for the design, development, and evaluation of novel cardiac rhythm technologies, including next-generation leadless and conduction system pacing devices. This role supports R&D and R&T programs, contributing to prototype testing, clinical evidence generation, and regulatory submissions.


Key Responsibilities

  • Develop strategies for pre-clinical and clinical feasibility studies of new cardiac devices, including planning, execution, data collection, analysis, and publication.

  • Manage global Key Opinion Leader (KOL) engagement to gather clinical insights, feedback on prototypes, and support iterative device testing.

  • Coordinate with internal stakeholders to generate clinical and testing reports for regulatory submissions.

  • Drive clinical evidence generation that informs and impacts clinical practice with novel technologies.

  • Support R&D teams in the translation of innovative cardiac device concepts into clinically validated solutions.


Minimum Qualifications

  • MD or PhD with a cardiovascular background or expertise.

  • Strong knowledge of medical device quality systems and regulatory standards.


Preferred Qualifications

  • 12+ years of experience in Electrophysiology (EP) / Cardiac Rhythm Management (CRM) industry.

  • Proven experience in clinical research, medical device evaluation, and evidence generation.


Compensation & Benefits

  • Base pay range: $172,000 – $344,000, depending on location.

  • Comprehensive health and wellness benefits to support you and your family.

  • Career development opportunities in a global, innovative healthcare organization.