Project Manager
1 week ago
**Responsibilities**:
- Creating and maintaining regulatory submission timelines, reports, and trackers
- Assisting in the coordination between departments in the preparation of dossiers
- Formatting and quality review of electronic common technical dossiers
- Reviewing of all regulatory agency submission materials to ensure timeliness, accuracy, comprehensiveness, and compliance with regulatory standards
- Performing miscellaneous job-related duties as assigned by Head of Department
- Supporting overall team projects in Regulatory & Medical Affairs Department
**Job Requirements**
- Degree in Life Science or equivalent
- Minimum 5 years’ experience in clinical research and pharmaceutical or CRO industries
- Must be highly organized and have the ability to meet critical timelines
- Able to work as part of a team and achieve assigned timelines
- Very strong organizational skills that is necessary to manage and multi-task various activities
- Good communication skills and must be fluent in both written and spoken English
- Good coordination skills and ability to establish and maintain effective working relationships with all levels within the company and third parties
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