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.
Study Start Up Associate
đ June 20
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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 Facilitate the initiation of clinical trials, ensuring compliance with regulatory requirements âą Deliver site start-up and activation work to a high standard, working closely with your team and stakeholders âą Assist in the preparation and submission of regulatory documents, such as clinical trial applications and ethics committee submissions âą Coordinate with internal and external stakeholders to obtain necessary approvals and authorizations for study initiation âą Maintain accurate and up-to-date records of regulatory submissions and approvals âą Support study teams in the development of study documents, including protocols, informed consent forms, and investigator brochures âą Participate in study start-up meetings and provide input on regulatory requirements and timelines
đŻ Requirements
âą Bachelor's degree in life sciences or a related field âą Must have experience in startup activities in clinical research (submissions, contracts and budget, site activation) âą Experience in Phase I submissions is highly preferred âą Strong attention to detail and organizational skills âą Ability to work independently and manage multiple tasks simultaneously in a fast-paced environment 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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