A leading clinical research organization in the UK is seeking a Study Start Up Associate II to lead the initiation of clinical trials. The role involves preparing regulatory documents, coordinating with stakeholders, and ensuring compliance with regulatory requirements. Candidates should have a Bachelors degree in life sciences and a minimum of 2 years of experience in clinical research or regulatory affairs, focusing on study start-up activities. ICON values diversity and offers competitive benefits for work-life balance.
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