About this role
Job title: Senior Study Start Up Associate - Sponsor Dedicated
About the Role Senior Study Start Up Associate at ICON supports the Study Start Up Team Lead in developing and executing plans for country and site distribution within a large-scale, fast-paced environment.
What You'll Do
- Lead on site start-up and activation tasks requiring technical depth, with a focus on quality and continuous improvement.
- Efficiently drive study initiation: conduct feasibility assessments, site identification, site contract negotiation, and other critical SSU activities.
- Empower success through specialized SSU expertise: provide expertise to Study Start Up team leads and project teams, offering valuable insights to drive success.
- Ensure regulatory compliance: prepare and coordinate submissions to regulatory, ethics, and other relevant bodies, ensuring compliance with regulations and guidelines.
- Safeguard patient welfare: contribute to the development, finalization, and review of Master and Country Specific Subject Information Sheets/Informed Consent Forms, guaranteeing patient safety and informed consent.
What We're Looking For
- 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.
- Fluency in the local language and English.
- Willingness to travel as required (approximately 5%).
Compensation & Benefits
- Competitive salary with a range of benefits focused on well-being and work-life balance.
- Annual leave entitlements, health insurance options, retirement planning offerings, and LifeWorks Global Employee Assistance Programme (EAP).
- Life assurance and flexible country-specific optional benefits (e.g., childcare vouchers, gym memberships, subsidized travel passes, health assessments).
- ICON is committed to inclusion, equal opportunity, and accessibility for all candidates.