Job Description
Key Responsibilities:
- Act as the primary point of contact for assigned protocols, integrating efforts between Country Operations and the Clinical Trial Team (CTT)
- Proactively manage project timelines and performance metrics for assigned studies, ensuring all country commitments are met
- Review Monitoring Visit Reports, escalating performance issues and training needs to the appropriate managers as necessary
- Lead local study teams, providing training and support on the protocol to enhance team performance
- Create and execute a local risk management plan for assigned studies
- Ensure compliance with Clinical Trial Management System (CTMS), Electronic Trial Master File (eTMF), and other essential systems
- Collaborate with functional outsourcing vendors, investigators, and external partners to facilitate the success of assigned studies
- Act as the country point of contact for programmatically outsourced trials.
- Build and maintain business relationships with investigators and serve local business needs as applicable
- Support local and regional strategy development aligned with long-term corporate objectives
- Collaborate with internal teams, including HQ functions, regional operations, and Global Medical Affairs, to address key issues across clinical trials
Experience Requirements:
- Significant experience in clinical research
- Previous CRA or CRM experience is desirable
Educational Requirements:
- Bachelor's degree in Science or a comparable field is required
Current Contingent Workers apply
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