Offer summary
Qualifications:
High/Secondary school diploma or equivalent, Bachelor's degree preferred, Knowledge of SSU/Regulatory processes, Good English and local language skills, Proficient in MS Office and clinical trial databases.
Key responsabilities:
- Provide administrative and technical support to Project Team
- Ensure files are reviewed for audit readiness
- Coordinate trial activities according to the task matrix
- Communicate risks and perform timely document processing
- Assist in site activation and regulatory submissions