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Regulatory Submissions Manager

Key Facts

Remote From: 
Full time
Senior (5-10 years)
English

Other Skills

  • •
    Collaboration
  • •
    Leadership

Roles & Responsibilities

  • Bachelor's degree in a scientific or healthcare-related field; advanced degree preferred
  • Minimum of 6 years of experience in regulatory affairs within the pharmaceutical or biotech industry
  • Prior experience with various regulatory submissions, including CTA/IND/MAA
  • Strong understanding of global regulatory requirements and guidelines

Requirements:

  • Lead regulatory activities and submissions independently
  • Provide regulatory guidance and efforts to internal teams
  • Participate in agency interactions and regulatory submissions
  • Contribute to developing best practices within ICON Regulatory Affairs

Job description

Regulatory Submissions Manager

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 Manager, Regulatory Affairs to join our diverse and dynamic team. As a Manager, Regulatory Affairs at ICON, you will play a pivotal role in contributing to drug development as part of the Regulatory Affairs team. You'll provide regulatory guidance and operational support across various stages of drug development, including early development, agency interactions, clinical trial applications, marketing applications, and post-approval staff.


What you will be doing

  • Lead regulatory activities and submissions independently, with prior experience in areas such as CTA/IND/MAA
  • Provide regulatory guidance and efforts to internal teams
  • Participate in agency interactions and regulatory submissions
  • Contribute to developing best practices within ICON Regulatory Affairs through your insight of regulatory processes and guidelines
  • Work collaboratively as part of a regulatory or cross-functional team, depending on project size and nature

Your profile

  • Bachelor's degree in a scientific or healthcare-related field; advanced degree preferred
  • Minimum of 6 years of experience in regulatory affairs within the pharmaceutical or biotechNlogy industry
  • Prior experience with various regulatory submissions, including CTA/IND/MAA
  • Ability to lead internal teams and carry out regulatory activities independently
  • Strong understanding of global regulatory requirements and guidelines

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

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