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Jobgether
Overview
Support regulatory affairs and patient safety activities, including labeling operations, submissions, and compliance documentation. Collaborate with global cross-functional teams to ensure adherence to international regulatory and pharmacovigilance standards.
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Compensation
Salary not listed
Posted
6 days ago
Xenon Pharmaceuticals
Lead and manage clinical development studies in psychiatry. Serve as medical monitor and interact with global research sites. Contribute to clinical development plans and strategies. Provide scientific leadership for trial designs. Review scientific literature and develop product knowledge. Maintain awareness of external research and regulatory environments. Build relationships with Key Opinion Leaders. Draft and review regulatory submissions and scientific publications. Interpret clinical trial data and provide clinical relevance insights. Support in-licensing and out-licensing activities. Present proposals to senior management. Develop departmental goals and manage budgets. Collaborate with external vendors and stakeholders. Lead and develop team members (if any)
$344,000 - $380,400 / YEAR
3 months ago
