Expertise
What I do, and to what standard
Study operations, quality systems, regulatory submissions, and market intelligence — across Phase I–IV and non-interventional work.
Study operations
Phase I–IV and non-interventional, feasibility through closeout
Quality systems
ICH-GCP-aligned SOPs and quality management
Regulatory
Submissions, site management, sponsor communications
Market intelligence
Clinical catalysts, competitive and M&A analysis
How it works
Engagement sequence
I handle vendor scouting, screening, and negotiation, so you land with the right partner the first time instead of the third.
You tell me the study
Therapeutic area, phase, target enrollment, budget envelope, and your timeline constraints. Thirty minutes is usually enough.
Output — a candid read on whether the Philippines fitsI shortlist and negotiate
I run competitive proposals across vetted Philippine CROs and negotiate pricing and timelines on your behalf. You see the comparison, including the partners I ruled out and why.
Output — a costed shortlist with negotiated termsYou sign; I stay on
You contract directly with the CRO. I remain engaged as your local advisor through startup and execution — the person who reads the room when a site goes quiet.
Output — ongoing local representation
How the work is held to account
ICH-GCP-aligned SOPs, documented quality management, and submissions that survive a sponsor’s audit.