Worldwide Clinical Trials in the United Kingdom is seeking a Clinical Research Associate to manage research activities at sites participating in registries and other non-interventional studies across the full study lifecycle.
You will perform SIVs, train sites, collect regulatory documents, and support contracts/budgets, with travel required. Strong English, organization, and proficiency in MS Office, CTMS and EDC are essential.
This is a genuine opening to take on the Senior Clinical Research Associate - UK (Oncology/CNS) role at Worldwide Clinical Trials.
Full responsibilities and requirements are described in the listing above.
Learn more about the Senior Clinical Research Associate - UK (Oncology/CNS) role in the description above.
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