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ICON plc

Senior Validation Analyst (Veeva EDC)

Posted 2 hours ago
5-10 years experience
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AI Summary

You will lead scientific operations tasks by developing and executing validation plans, protocols, and reports for systems to ensure regulatory compliance. Additionally, you will collaborate with IT and QA teams to conduct risk assessments and provide guidance to junior analysts.

Senior Validation Analyst (Veeva EDC) - Office or Home based

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.


As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.


As a Senior Validation Analyst at ICON, you will be responsible for ensuring that all systems and processes comply with regulatory standards and internal quality requirements.


What You Will Do:

You will lead on scientific operations tasks requiring technical depth, with a focus on quality and continuous improvement.

Key responsibilities include:

  • Developing and executing validation plans, protocols, and reports for software, systems, and processes to ensure compliance with regulatory requirements.
  • Collaborating with IT, QA, and operational teams to assess validation needs and establish best practices in validation methodologies.
  • Conducting risk assessments and impact analyses to identify potential issues and recommend appropriate validation strategies.
  • Documenting validation activities and maintaining accurate records to support audits and inspections.
  • Providing training and guidance to junior analysts, fostering a culture of quality and compliance within the team.

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 Life Sciences, Engineering, Computer Science, or a related field.
  • Extensive experience in validation activities within the healthcare, pharmaceutical, or clinical research sectors.
  • Strong knowledge of regulatory requirements (e.g., GxP, FDA, EMA) and validation best practices.
  • Excellent analytical and problem-solving skills, with a keen attention to detail and accuracy.
  • Effective communication skills, with the ability to collaborate with cross-functional teams and convey complex information clearly.
  • Willingness to travel as required (approximately 5%)

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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