ICON plc
10,000+ employees
Founded 1990
đ Pharmaceuticals
𧏠Biotechnology
âïž Healthcare Insurance
Pharmaceuticals âą Biotechnology âą Healthcare Insurance
ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.
Senior Study Start Up Associate
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ICON plc
10,000+ employees
Founded 1990
đ Pharmaceuticals
𧏠Biotechnology
âïž Healthcare Insurance
Pharmaceuticals âą Biotechnology âą Healthcare Insurance
ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.
đ Description
âą Lead on site start-up and activation tasks requiring technical depth âą Conduct feasibility assessments, site identification, site contract negotiation, and other critical SSU activities âą Provide expertise to Study Start Up team leads and project teams âą Prepare and coordinate submissions to regulatory, ethics, and other relevant bodies âą Contribute to the development, finalization, and review of Master and Country Specific Subject Information Sheets/Informed Consent Forms
đŻ Requirements
âą A Bachelor's degree or local equivalent and/or appropriate experience from the Medical/science background and/or discipline âą At least 3 years of experience or understanding of clinical study start-up requirements and activities âą Fluency in the local language and English is essential âą Willingness to travel as required (approximately 5%)
đïž Benefits
âą Competitive base salary and performance related incentives âą Health and wellbeing programmes including medical, dental, and vision coverage where applicable âą Retirement and pension plans âą Life assurance and disability coverage âą Employee assistance programmes and wellbeing resources âą Learning and development opportunities through structured training and career pathways
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