ICON plc

Senior Informed Consent Specialist

ICON plc$95K — $115K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • Extensive experience in clinical research, regulatory affairs, ethics, or informed consent
  • In-depth knowledge of GCP, ethical principles, and global regulatory expectations
  • Exceptional writing and editing skills for concise, patient-friendly documentation
  • Strong stakeholder management skills, capable of liaising with sponsors, IRBs/ECs, and teams
  • Proven ability to manage multiple complex studies accurately

Responsibilities

  • Lead the creation and optimization of informed consent forms for complex studies
  • Advise study teams on informed consent strategies considering cultural and regulatory factors
  • Oversee translation and version control for consistency across regions
  • Interact with sponsors and ethics committees to resolve consent-related queries
  • Develop guidance and training materials to promote standardization
  • Mentor junior team members and contribute to process improvements

Benefits

  • Comprehensive total rewards package for health and wellbeing
  • Health programmes including medical, dental, and vision coverage
  • Retirement and pension options
  • Life assurance and disability coverage
  • Employee assistance and wellbeing resources
  • Learning and development opportunities including training and career pathways
Full Job Description
Informed Consent Specialist I

As a Senior Informed Consent Specialist at ICON, you will lead the development and oversight of informed consent strategies and documents for complex, global clinical studies. You will act as a subject matter expert, ensuring participant-facing materials are ethical, compliant, and understandable.


What You Will Do:

You will take ownership of scientific operations deliverables, applying your expertise to complex challenges.

Key responsibilities include:

  • Leading the creation, review, and optimisation of global and country-specific informed consent forms for complex or high-risk studies.
  • Advising study teams on informed consent strategies, including readability, cultural considerations, and local regulatory expectations.
  • Overseeing translation, localisation, and version control processes to ensure consistency and traceability across regions.
  • Interacting with sponsors, ethics committees, and regulatory authorities to address consent-related queries and negotiate wording as needed.
  • Developing guidance, templates, and training materials to drive standardisation and best practices within the informed consent function.
  • Mentoring junior informed consent specialists and contributing to continuous improvement initiatives.

Your Profile:

You will have a strong foundation in scientific operations, with the experience to work independently and guide others.

Required qualifications and experience:

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • Extensive experience in clinical research, regulatory affairs, ethics, or a related area with strong focus on informed consent.
  • In-depth knowledge of GCP, ethical principles, and global regulatory expectations for participant information and consent.
  • Exceptional writing and editing skills, with the ability to produce clear, patient-friendly documents.
  • Strong stakeholder management skills, with experience liaising with sponsors, IRBs/ECs, and cross-functional teams.
  • Proven ability to manage multiple complex studies and deadlines with a high degree of accuracy and ownership.

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 to read more about the benefits ICON offers.


Are you a current ICON Employee? Please click to apply

About ICON plc

ICON plc is a global provider of drug development and commercialisation services to the pharmaceutical, biotechnology and medical device industries. The company specialises in the strategic development, management and analysis of programs that support clinical development. ICON has approximately 15700 employees in 40 countries. The company was founded in Dublin, Ireland in 1990 and is headquartered in Leopardstown, Dublin. ICON has been publicly traded on the NASDAQ since 1998.
Learn more about ICON plc
Size
39,300 employees
Market Cap
$16.2 billion
Industry
Net Income
$332.3 million
Founded
2017
5 Year Trend
+26.9%
Revenue
$2.7 billion
NASDAQ

Similar Jobs

More Jobs at ICON plc

More Pharmaceuticals & Biotech Jobs

Find similar Senior Informed Consent Specialist jobs: