CTRC is proud to have a dedicated team of full-time Clinical Research Coordinators (CRCs) who are trained in Good Clinical Practice (GCP) and adhere strictly to ICH-GCP guidelines, as well as other regulatory requirements. Our CRCs are committed to ensuring the highest standards of quality, safety, and ethical conduct in all clinical studies.
Our team holds the following qualifications and certifications:
With extensive experience in managing clinical drug trials from Phase I to IV, medical device studies and observational studies, our CRCs work closely with Principal Investigators (PIs), Industry Sponsors, and Contract Research Organizations (CROs) across various therapeutic areas.
At CTRC, we ensure the long-term continuity of our staff, fostering the retention of multidisciplinary knowledge and expertise, which we continuously enhance through ongoing professional development.
Our CRCs bring specialised skills as:
CTRC’s CRC team provides exceptional support for both investigator-initiated trials and pharmaceutical-sponsored studies. If you are interested in collaborating with CTRC or require manpower for your research study, please contact us for further discussions.
Contact Our Feasibility Team!
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