Take the lead in pioneering global clinical studies that positively impact patient lives. Work remotely and manage complex projects from inception to close-out with agility and expertise.In this role, you'll lead large-scale clinical studies, serving as the primary contact for stakeholders. Your expertise will ensure compliance with regulatory standards and manage vendor oversight throughout the study lifecycle. Collaboration across cross-functional teams is vital as you develop essential documents, support site engagements, and monitor study quality.Key Responsibilities:• Oversee complex clinical study activities from start to finish• Act as the main point of contact for stakeholders• Develop study documents such as protocols and monitoring plans• Manage vendor qualifications and engagement throughout studies• Ensure compliance with regulatory requirementsRequirements:• Bachelor’s degree in a related field is required• GCP certification and knowledge of regulatory standards• 6+ years of clinical study management experience• Strong project management and leadership skills• Excellent communication and relationship-building abilitiesEmbrace the opportunity to shape clinical research and enhance patient care while fostering collaboration and innovation.#J-18808-Ljbffr
Lead Clinical Study Manager For Global Research Initiatives
SMITH+NEPHEW
mississauga, mississauga
Published 27 days ago
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