
Global Clinical Project Coordinator
2 semanas atrás
Oversee interdisciplinary clinical research studies to ensure compliance with regulatory requirements.
Responsibilities:- Manage projects, overseeing clinical research studies and ensuring adherence to Good Clinical Practice (GCP) guidelines and relevant SOPs.
- Act as primary liaison between stakeholders to facilitate timely study launch, conduct, and closeout according to contractual agreements.
- Lead cross-functional teams to drive quality, timelines, and budget management.
- Accountable for financial performance of each project, including identifying and mitigating risks.
- Coordinate activities and deliverables of all study conduct partners, proactively managing issues and resolving conflicts.
- Ensure studies are conducted in compliance with GCP, relevant SOPs, and regulatory requirements, promoting a culture of quality and excellence.
- Bachelor's Degree or equivalent qualification in life sciences, medicine, pharmacy, nursing, or an equivalent combination of education and experience.
- Clinical research organization (CRO) and therapeutic area expertise preferred.
- Strong knowledge of Good Clinical Practice/ICH guidelines, regulations, and industry standards.
- Excellent organizational skills, with the ability to manage time effectively and work independently.
- Direct therapeutic area expertise, with a deep understanding of disease mechanisms and treatment options.
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