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Senior Clinical Research Associate – Cardiovascular Medical Device Trials | Icon Plc

Icon Plc
ICON PLC
3+ years
Not Disclosed
Remote, USA, Remote
1 May 7, 2026
Job Description
Job Type: Full Time Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Clinical Research Associate – Cardiovascular Medical Device Trials | ICON plc

Company: ICON plc
Job Title: Senior Clinical Research Associate (Senior CRA) – Cardio Medical Device
Location: United States (Remote)
Job Type: Full-Time
Work Mode: Remote
Job Requisition ID: JR142914


About ICON plc

ICON plc is a globally recognized Clinical Research Organization (CRO) specializing in healthcare intelligence, pharmaceutical development, biotechnology research, and medical device clinical trials. The company partners with leading healthcare organizations worldwide to accelerate innovative therapies and improve patient outcomes through advanced clinical research solutions.

ICON provides exceptional career opportunities across:

  • Clinical Operations
  • Medical Device Research
  • Cardiovascular Studies
  • Clinical Monitoring
  • Regulatory Affairs
  • Pharmacovigilance
  • Data Management

Job Overview

ICON plc is seeking an experienced Senior Clinical Research Associate (Senior CRA) to support a cardiovascular/electrophysiology medical device clinical study in the United States.

The selected candidate will oversee site monitoring activities, maintain regulatory compliance, ensure patient safety, and support successful execution of cardiovascular clinical trials.

This role is ideal for professionals experienced in:

  • Cardiovascular medical device studies
  • Electrophysiology trials
  • Cardiology clinical research
  • Clinical monitoring and site management

Experience Required

Mandatory Experience

  • Minimum 3 years of clinical trial monitoring experience

Preferred Experience

  • Cardiovascular medical device monitoring experience preferred
  • Electrophysiology clinical trial experience preferred
  • Cardiovascular pharmaceutical monitoring experience will also be considered

Freshers Eligibility

  • Freshers are NOT eligible
  • Prior CRA monitoring experience is mandatory

Educational Qualification

Required Degree

Bachelor’s degree required, preferably in:

  • Life Sciences
  • Biological Sciences
  • Physical Sciences
  • Nursing
  • Healthcare-related discipline

Therapeutic Area

Clinical Specialization

  • Cardiovascular Clinical Trials
  • Electrophysiology Research
  • Medical Device Studies
  • Cardiology Clinical Monitoring

Key Responsibilities

Clinical Trial Monitoring

  • Conduct and manage clinical monitoring activities
  • Ensure:
    • Protocol adherence
    • Data integrity
    • Patient safety
    • Regulatory compliance

Regulatory Compliance

  • Maintain compliance with:
    • FDA regulations
    • ICH-GCP guidelines
    • Clinical trial SOPs

Site Relationship Management

  • Build strong relationships with:
    • Investigators
    • Site coordinators
    • Clinical study teams
    • Sponsors

Risk & Issue Management

  • Identify site risks and operational issues proactively
  • Implement corrective and preventive actions effectively

Clinical Documentation

  • Prepare accurate monitoring reports
  • Maintain high-quality trial documentation and records

Communication & Coordination

  • Coordinate effectively with internal and external stakeholders
  • Support communication planning across study teams and sites

Required Skills

Clinical Research Skills

  • Clinical Trial Monitoring
  • Cardiovascular Clinical Research
  • Medical Device Monitoring
  • Electrophysiology Studies
  • Site Management
  • Patient Safety Monitoring
  • Regulatory Compliance
  • FDA & ICH-GCP Knowledge

Technical Skills

  • CTMS
  • eTMF Systems
  • Clinical Trial Documentation
  • Clinical Data Review Tools

Soft Skills

  • Communication Skills
  • Stakeholder Management
  • Problem Solving
  • Attention to Detail
  • Organizational Skills
  • Time Management
  • Independent Working Ability