Develop clinical trial strategies, shaping study designs based on regulatory requirements, competitive insights and company's research interest. * Author and review study synopses and clinical trial protocols, regulatory documents, and study-related publications for clinical initiatives and grants. * Engage with (KOLs) and physicians who lead IITs (investigator initiated trials) and/or work on scientific projects, fostering strong scientific collaborations. * Strong quality attitude; comfortable in working with other departments of the company (e.g., Quality management, R&D, Marketing) * Confident handling of literature management tools (EndNote), databases for literature and Microsoft Office (Word, Excel, PowerPoint, Outlook, Visio etc.)
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