Description
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a Senior Study Start Up Associate at ICON, you will be working within a large-scale, fast-paced environment, supporting the Study Start Up Team Lead in developing and executing the plan for country and site distribution.
Responsibilities:
- Efficiently drive study initiation: conduct feasibility assessments, site identification, site contract negotiation, and other critical SSU activities.
- Empower success through specialised SSU expertise: provide expertise to Study Start Up team leads and project teams, providing valuable insights to drive success.
- Ensure regulatory compliance: prepare and coordinate submissions to regulatory, ethics, and other relevant bodies, ensuring compliance with all necessary regulations and guidelines.
- Safeguard patient welfare: contribute to the development, finalisation, and review of Master and Country Specific Subject Information Sheets/Informed Consent Forms, guaranteeing the highest standards of patient safety and informed consent.
Your Profile:
- A Bachelor's degree or local equivalent and/or appropriate experience from a medical/science background and/or discipline.
- At least 3 years of experience or understanding of clinical study start-up requirements and activities, showing your expertise in the field.
- Fluency in the local language and English is essential, enabling you to effectively communicate and collaborate with international teams.
- Willingness to travel as required (approximately 5%).
Rewards & Benefits
- 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.
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