Trial Management Professional
4 days ago
This is an exciting opportunity to join the ICON team as a clinical operations specialist responsible for managing global clinical trials. As a seasoned professional, you will leverage your extensive experience in trial management, data analysis, and project coordination to drive results-oriented projects forward.
Key Responsibilities:
- Oversee planning, execution, and reporting of clinical trials across different phases and therapeutic areas.
- Ensure accuracy and compliance through meticulous trial tracking system maintenance and analysis.
- Identify areas for improvement and implement process changes to optimize efficiency and quality.
- Develop and maintain a deep understanding of regulatory requirements, supporting compliant activities across the trial lifecycle.
- Provide guidance and training to junior team members, promoting knowledge sharing and collaboration.
- Foster relationships with internal and external partners, enhancing cooperation and knowledge exchange within the industry.
Your Profile:
- Associate or Bachelor's degree, preferably in a life sciences or business-related field.
- 2-3 years of experience in clinical operations, project management, or a related field, ideally within a CRO or pharmaceutical setting.
- Strong analytical skills, advanced Excel capabilities, and fluency in Microsoft Office tools.
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