Clinical Project Manager leading the planning and execution of Global Drug Development studies for Novartis in China. Collaborating with various teams to ensure compliance and timely delivery of studies.
About the role
- Scientist contributing to the scientific planning and execution of clinical trials within the ophthalmology field. Developing leadership, technical skills, and scientific acumen in a global team context.
Responsibilities
- Responsible for specific clinical/scientific activities on a single study or across multiple studies (e.g., medical monitoring, lab specimen tracking/reconciliation, adjudication support, preparation of meeting materials)
- Support development of Protocol and related study materials (e.g., ICF documents/amendments, data management deliverables)
- May interact with internal and external stakeholders (e.g., country operations, committees, vendors) in support of clinical study objectives
- Support development of site and CRA training materials
- Prepare clinical narratives
- Collaborate cross-functionally to monitor clinical study data to ensure quality, completeness, and integrity of trial conduct.
- Participate in CRF design to ensures data collection is in alignment with the protocol
Requirements
- Bachelor's Degree +2 years of pharmaceutical, clinical drug development, project management, and/or medical field experience OR Master's Degree +1 year of pharmaceutical, clinical drug development, project management, and/or medical field experience
- Degree in life sciences, preferred
- Ophthalmology experience required.
Benefits
- medical, dental, vision healthcare and other insurance benefits (for employee and family)
- retirement benefits, including 401(k)
- paid holidays
- vacation
- compassionate and sick days
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