Supporting Clinical Scientist for global studies. May serve as Study Leader and/or Clinical Scientist for low complexity global studies or local studies.
Proven ability to follow instructions and guidelines, work independently, and take initiative. Excellent attention to detail and accuracy in maintaining high-quality standards.
Strong knowledge of Quality Agreement / Technical Agreement drafting and review. Practical experience in vendor risk assessment, approved vendor list management and periodic vendor requalification.
Work as a partner with the global study leader to monitor study conduct and progress – identify, resolve, and escalate risks that impact delivery of the study against quality, timeline, and budget objectives.