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Assists in the preparation of conference calls, meetings, and conferences by developing agendas, coordinating participation, preparing and distributing materials, summarizing proceedings and tracking follow-up actions. Preparing reports, tables and data analysis for incorporation into broader documents and reports. Organize and maintain paper and electronic archived records of all committee business, correspondence and reviews.
- University degree
- A minimum of 1 year experience in clinical research or healthcare related industry
- Knowledge of ICH/GCP
- Proficient computer skills across multiple applications
- CRO, Pharmaceutical, Biotech, experience preferred
- Performs job duties with minimal guidance.
- Communicates with sites regarding trial start-up, conduct, and close-out activities
- Collects and reviews regulatory documents from clinical sites
- Initiates, maintains, and reconciles Trial Master File
- Organizes and maintains tracking systems and tools to support the conduct of a clinical study from start-up to close-out.
- Manages and tracks clinical/non-clinical supplies
- Effective English written and verbal communication skills
- Well organized and focus on details
- Prioritizes and multitasks to ensure that tasks are completed on time
- Effectively collaborates with team members
- Excellent working conditions
- Extensive training;
- Competitive salary & benefits package;
- Opportunities for personal & professional growth.
International Clinical Research Organization,
Premier Research has clinical operations teams in more than 30 countries, including Western, Central and Eastern Europe and North America.
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