Summary
About the Role
Key Responsibilities
- Support study start-up activities including document collection and tracking
- Assist in Trial Master File (TMF) maintenance and document uploads
- Maintain study trackers and support reporting activities
- Assist in meeting coordination, minutes, and follow-ups
- Support communication with internal stakeholders and sites
- Ensure compliance with SOPs, GCP, and training requirements
Key Deliverables
- Accurate and timely maintenance of study documentation
- High-quality TMF support and document filing
- Timely updates to study trackers and reports
- Compliance with training and SOP requirements
Qualifications
- Bachelor’s degree (or pursuing final year) in Life Sciences, Pharmacy, Nursing, or related field
- Basic understanding of clinical research preferred
Skills & Competencies
- Attention to detail and strong organizational skills
- Good communication and teamwork
- Basic MS Office skills (Excel, Word, PowerPoint)
- Ability to learn quickly and work in a structured environment
Languages :
- English.
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally.
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