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Job Description Summary
Job Description
- 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
- 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
- Bachelor’s degree (or pursuing final year) in Life Sciences, Pharmacy, Nursing, or related field
- Basic understanding of clinical research preferred
- 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.
Skills Desired
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