Training, consultancy, and talent solutions — each executed with the depth that only genuine sector expertise provides.
Clinical research in Malaysia and Singapore presents unique regulatory and operational challenges that generic frameworks don't always address. Our consultancy practice exists to close that gap.
We embed alongside your team — providing strategic thinking and ground-level operational expertise to help your studies run cleaner, faster, and in full regulatory compliance.
Review and redesign of clinical operations workflows to eliminate bottlenecks and improve study delivery timelines.
Preparation of sites, investigators, and sponsor teams for faster, cleaner study activation.
Development and review of the procedural infrastructure supporting inspection-ready clinical operations.
Ethics committee and regulatory agency submission support, IRB/IEC liaison, and regulatory guidance for both sponsors and CROs.
Engagement models: Retained advisory, project-based, or short-term embedded. Scoped to your specific situation. Start with a conversation →
Our programmes are designed for the realities of clinical research in the region — combining ICH-GCP compliance with practical, site-level application. Facilitated by experienced practitioners with real industry credentials — designed for pharma sponsors and CROs alike.
Available in-person, virtual, or blended. Customisable for your team's size, experience level, and therapeutic area.
All ORRA training programmes are facilitated by practitioners with extensive real-world clinical research experience — not academic trainers. Every session is grounded in actual industry practice.
From GCP to CRA: a practical bootcamp that teaches learners how CRA work is actually done — monitoring visits, site files, deviations, CAPA, reports.
Fully custom content built around your SOPs, therapeutic area, and team experience profile.
Certificate Notice: Upon completion of the training course, participants will receive a Certificate of Completion issued by ORRA Synergy. This certificate confirms completion of the training. It is not a Malaysian GCP certificate, regulator-issued certification, or professional licensure.
Upcoming cohorts: Training schedules will be published here. To register interest or discuss a bespoke programme, contact us →
Clinical research talent matching is different. The roles are specialised, the compliance implications of a wrong hire are significant, and the talent pool is genuinely limited. Generic platforms consistently miss the mark.
We understand what competency skills are required for each role. Our matching is built on demonstrated competency, not keyword searches.
Talent Solutions Platform — Coming Soon
Our talent solutions platform is currently under development. Contact us to express your interest in the meantime.
Monitoring professionals at all levels — junior through senior and lead CRA, across therapeutic areas.
CTMs and CPMs with hands-on trial management experience.
Regulatory submission specialists experienced in CTA submissions and ethics committee applications.
Short-term project support through to permanent executive search — scoped to your need.