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ICON plc

Clinical Scientist - Veeva EDC

Posted 3 hours ago
2-5 years experience
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AI Summary

The Clinical Scientist will design and implement clinical trial protocols while ensuring adherence to scientific and regulatory standards. They will also manage the transition to Veeva EDC and collaborate with cross-functional teams to ensure high-quality study execution and data analysis.

Clinical Scientist - Veeva EDC

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 Clinical Scientist at ICON, you will design and conduct clinical studies that advance our understanding of new therapies.


What You Will Do:

You will take responsibility for clinical research deliverables, applying your skills to ensure quality and efficiency.

Key responsibilities include:

  • Support the EDC transition, leveraging strong hands-on experience with Veeva EDC to ensure a smooth and effective transition.
  • Apply a clinical monitoring background, ideally as a CRA and/or CTM, to support clinical study activities, data quality, and operational requirements throughout the transition.
  • Designing and implementing clinical trial protocols, ensuring adherence to scientific and regulatory standards.
  • Conducting data analysis and interpretation to derive insights that support study objectives.
  • Collaborating with cross-functional teams to ensure effective study execution and data quality.
  • Engaging with stakeholders to communicate findings and contribute to scientific discussions.


Your Profile:

You will bring relevant clinical research experience, along with the following qualifications and skills.

Required qualifications and experience:

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • CRA/monitoring background with Veeva EDC experience are welcomed
  • Experience in clinical research or a related scientific role, with a strong understanding of clinical trial processes.
  • Excellent analytical skills and proficiency in data interpretation and statistical analysis.
  • Strong communication and collaboration skills, with the ability to work effectively in interdisciplinary teams.

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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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