Global Study Manager

Leading the management of global oncology studies, the full-time salaried Global Study Manager will oversee study document preparation, facilitate internal and external interactions, and ensure compliance with clinical guidelines while working remotely. Key responsibilities Oversee the preparation of study documents and maintain interactions with internal and external stakeholders to ensure efficient study delivery Contribute to risk identification and develop mitigation plans, ensuring all study documents are complete and verified for quality Support budget management and project management activities, ensuring adherence to timelines, budget, and quality standards Required qualifications University degree in medical or biological sciences or a related field At least 3 years of relevant experience in the pharmaceutical industry or clinical research Experience in global study management with a focus on vendor and external partner management Strong knowledge of ICH/GCP guidelines and the clinical development process Demonstrated leadership and project management skills, with early phase oncology experience required