Study Start Up Associate I

About the role

As a Study Start Up Associate I at ICON, you will facilitate the initiation of clinical trials, ensuring compliance with regulatory requirements and supporting the development of innovative treatments.

Key responsibilities

• Assist in preparing and submitting regulatory documents such as clinical trial applications and ethics committee submissions.
• Coordinate with internal and external stakeholders to obtain approvals and authorizations for study initiation.
• Maintain accurate records of regulatory submissions and approvals.
• Support study teams in developing study documents, including protocols, informed consent forms, and investigator brochures.
• Participate in study start‑up meetings and provide input on regulatory requirements and timelines.

Required profile

• Bachelor's degree in life sciences or a related field.
• Strong attention to detail and organizational skills.
• Excellent communication and interpersonal abilities.
• Ability to work independently and manage multiple tasks in a fast‑paced environment.

What we offer

• 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.