Hiring.Camp

Medical Director (Cardiology)

Icon Plc

·

Today

Location
US, Blue Bell (ICON), United States of America · US, Raleigh, NC
Workplace
Onsite
Type
Full-time
Department
Healthcare
Seniority
Director
Source
Workday

Description

Medical Director (Cardiology)- United States or Mexico- Remote

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


We are currently seeking a Medical Director specializing in Cardiology to join our Biotech Medical Affairs team.


As a Medical Director at ICON, you will serve as a key medical and scientific partner to our biotech clients, providing therapeutic expertise throughout the lifecycle of clinical development programs. Working within a fast-paced, client-focused environment, you will partner closely with sponsors and cross-functional project teams to provide medical oversight, support clinical development strategy, and help navigate the medical and scientific considerations that arise throughout study delivery.


This role offers the opportunity to work closely with emerging and established biotech companies, bringing your clinical Cardiology expertise into clinical research while helping sponsors advance important cardiovascular programs.


What You Will Be Doing

  • Provide medical and scientific leadership across clinical development programs within Cardiology.
  • Serve as a trusted medical partner to biotech sponsors and ICON project teams throughout the study lifecycle.
  • Provide medical monitoring and expert consultation on patient safety, eligibility, protocol-related questions, and other clinical issues arising during study conduct.
  • Support the interpretation and application of study protocols from a medical and scientific perspective.
  • Partner with Clinical Operations, Safety, Regulatory, and other cross-functional teams to identify and address medical risks that could impact study delivery.
  • Provide therapeutic and scientific input into clinical development strategies and study planning.
  • Participate in client meetings and provide medical expertise during proposal development, bid defenses, and other business development activities.
  • Ensure medical and safety monitoring activities are conducted in accordance with applicable ethical, regulatory, and quality standards.

Your Profile

  • Medical degree (MD or equivalent) required.
  • US Board certification in Cardiology required.
  • Clinical practice experience as a Cardiologist.
  • Experience in clinical research, clinical trials, or drug development, ideally within a pharmaceutical, biotechnology, or CRO environment.
  • Strong knowledge of cardiovascular medicine and the ability to apply clinical expertise within a clinical research setting.
  • Understanding of GCP and the regulatory and ethical requirements associated with clinical trials.
  • Strong communication skills with the ability to work effectively with biotech sponsors, investigators, and global cross-functional teams.
  • Comfortable working in a client-facing environment where priorities may evolve as programs progress.
  • Willingness to travel approximately 10–15%, as required.

** This is a remote role.



#LI-MN1

#LI-Remote


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply

Skills

GCPClinical Trials

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