Senior Study Start Up Associate
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Job Description
Senior Study Start Up Associate at ICON managing clinical research site start-up processes in a fast-paced environment. Leading site activation tasks and ensuring regulatory compliance with top-notch patient safety standards.
Responsibilities:
- Lead on site start-up and activation tasks requiring technical depth
- Conduct feasibility assessments, site identification, site contract negotiation, and other critical SSU activities
- Provide expertise to Study Start Up team leads and project teams
- Prepare and coordinate submissions to regulatory, ethics, and other relevant bodies
- Contribute to the development, finalization, and review of Master and Country Specific Subject Information Sheets/Informed Consent Forms
Requirements:
- A Bachelor's degree or local equivalent and/or appropriate experience from the 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 is essential
- Willingness to travel as required (approximately 5%)
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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