Job Description Summary

Job Description

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

- Bachelors 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.

Skills Desired