Location
remote, romblon, Philippines
Posted
July 04, 2026
Job Description
Position Overview
We are seeking a Clinical Research & Technical Associate (CRA/CTA) to join a dynamic, science-driven consulting environment. This role combines on-site monitoring responsibilities with essential administrative and documentation support across the full lifecycle of observational studies.
The successful candidate will play a key role in ensuring quality, regulatory compliance, and data integrity, acting as a central point of coordination between investigators, sponsors, project managers, and ethics committees.
Key Responsibilities
Study Start-Up & Regulatory Affairs
- Prepare, compile, and submit study documentation to Ethics Committees (CEIm) and relevant regulatory authorities in accordance with applicable legislation (e.g., Royal Decree 957/2020, GDPR).
- Draft, review, and track contracts, amendments, and informed consent forms.
- Coordinate site initiation activities, including preparation of study sta...