Clinical Research Consulting
Freelance Clinical Trial Management
Our freelance clinical trial management service provides flexible, expert clinical research consultancy tailored to the needs of small biotech firms, independent investigators, private clinics, and research start-ups.
Our services are designed to guide clients through the complexities of clinical trial planning, study start-up, and regulatory compliance without the overhead of a full-service CRO.
Scope of Work
Clinical Trial Planning
Regulatory and Ethics Strategy
Site Setup and Trial Feasibility
Project Management Support
Clinical Operations Advice
Stakeholder Engagement and Coordination
Audit preparation and support
Clinical Trial Virtual Assistant
Our clinical trial virtual assistant service provides reliable, GCP-compliant remote administrative support for clinical trial sites and sponsors.
Our services are designed for busy research teams, ensuring accurate documentation, streamlined scheduling, and consistent record-keeping. Our goal is to help sites remain audit-ready without needing additional onsite staff.
Scope of Work
Remote Trial Administration
Clinical Research Associate Freelance Support
Clinical Trial Management Support
eTMF Maintenance
Meeting Coordination and Minute Taking
Preparation of Site Documents and Logs
GCP-Compliant Record Keeping
Ethics Application Support
Our ethics application support services offer expert guidance, document preparation, and submission support for clinical research ethics applications, tailored to meet the specific requirements of Human Research Ethics Committees (HRECs) and Institutional Review Boards (IRBs).
This service is ideal for small teams, clinicians, or first-time researchers needing hands-on help navigating complex compliance processes.
Scope of Work
Document Preparation and Review
Application Form Completion
Submission Support
Post-Submission Follow-up