Global Study Manager, Oncology (BB-8CBEC)
Gefunden in: Xpatjobs CH
Beschreibung:Main Responsibilities:Developing operational plans, creating and managing clinical study budget and overseeing the consistency of operations;Managing relationships with vendors and cross-functional stakeholders. Oversee performance of vendors and third-party providers;Establishing yourself as a leader within the team, being recognized as a thought leader who inspires others to perform at their best and learn from best practices. Youll be shaping our capabilities and evolving your role overtime;Developing site monitoring and risk mitigation strategies and ensuring your team adheres to all appropriate standards, including ICH/GCP and other regulations;Overseeing the resource management, forecast and maintenance of supplies needed to ensure sites have the necessary supplies to run clinical studies;Leading feasibility assessments to ensure countries and sites are selected for participation in trials. Provide guidance to country operational reps during trials. Qualifications and Experience: Relevant working/residency permit or Swiss/EU-Citizenship required;Minimum Bachelors Degree in Life Sciences;Minimum of 3/4 years in clinical trial management (working knowledge of drug development process and respective regulations, including ICH and GCP guidelines);Experience with budget management & oversight;Have a growth mind-set and are excited about learning through experience;Feel comfortable thinking on your feet and thrive in fast-paced, ambiguous and highly collaborative environments;You are talented and passionate. You are inspired by our mission and would fit in well with our collaborative, rigorous and entrepreneurial spirit.
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