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.
Assisting in the preparation of regulatory submissions, study reports, and scientific publications.

Advanced degree in life sciences, medicine, or a related field.
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.
Detail-oriented and committed to maintaining high standards of data integrity and quality.

ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

What ICON can offer you:
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.

2 Icon Plc jobs in England & Wales