Clinical Scientist - Veeva EDC

ICON Clinical Research; Reading; Remote; GBP 40,000 - 70,000; Full time

Job summary

ICON Strategic Solutions is seeking a Clinical Scientist to lead and support clinical studies, focusing on Veeva EDC transitions and data quality across sponsor-dedicated projects. You will design, conduct, and monitor studies to advance new therapies while collaborating with multidisciplinary teams.

The role requires hands-on Veeva EDC expertise, strong analytical abilities, and effective communication with stakeholders to ensure high-quality deliverables in a fast-paced environment.

Qualifications

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

Responsibilities

• Take responsibility for clinical research deliverables to ensure quality and efficiency.
• Support the EDC transition with hands-on Veeva EDC experience.
• Apply a clinical monitoring background to support study activities and data quality.
• Design and implement clinical trial protocols with adherence to standards.
• Conduct data analysis to derive insights for study objectives.
• Collaborate with cross-functional teams and communicate findings to stakeholders.

Skills

Veeva EDC experience

CRA/monitoring background

Analytical skills

Communication skills

Education

Bachelor's degree in a relevant field

Job description

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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What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site (https://careers.iconplc.com/benefits) to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here (https://careers.iconplc.com/reasonable-accommodations)