Parexel International is seeking a Site Activation Partner to lead or support operational activities from study start-up to close-out for assigned sites, ensuring compliance with ICH/GCP, sponsor standards, and study timelines.
Responsibilities include initiating and coordinating documents for the Investigator Initiation Package (IIP), resolving site issues, coordinating with regulatory groups, updating clinical trial systems, and proactive site performance monitoring.
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Study Start-Up & Site Activation Specialist employer: Parexel International
At Parexel International, we pride ourselves on being an excellent employer by fostering a collaborative and innovative work culture that empowers our employees to thrive. With a focus on professional growth, we offer extensive training and development opportunities, ensuring that our team members can advance their careers while making a meaningful impact in the clinical research field. Located across Canada, our remote positions provide flexibility and the chance to work with diverse teams, enhancing both personal and professional experiences.
