
Senior Clinical Trial Regulatory Specialist
1 week ago
At our organization, we strive to deliver impactful and meaningful results in the pursuit of improving health worldwide. This dedication is a driving force that unites us and fuels our passion for excellence.
- Key Responsibilities:
- Manage clinical trial studies and serve as Regulatory Lead for global trials, with specific exposure to the European market.
- Provide expert guidance to project team members and work within broad project guidelines to facilitate issue and conflict resolution.
- Prioritize personal workload and may prioritize the project team's workload to achieve project scope and objectives.
- Seize opportunities to enhance project efficiency, results, or team performance and take proactive action.
- Utilize information from previous projects or client work to efficiently complete assigned project activities and facilitate business decisions.
- Deliver quality work that meets client expectations and review colleagues' work for content and quality to ensure high standards are met.
- Assess project issues and develop strategies to achieve productivity, quality, and project goals and objectives.
- Actively manage performance, including typical HR activities for direct reports (e.g., performance reviews, salary actions, bonuses, scorecards).
- Ensure policies and procedures are communicated to line personnel in accordance with local country regulations.
- Provide a comprehensive range of technical and business consulting services, primarily in areas with clear policy or precedent.
- Define self-development activities to stay current in the industry (e.g., maintain membership in relevant industry and/or scientific/technical associations).
Our commitment to improving health worldwide unites us, driving our dedication to deliver impactful and meaningful results.
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