CTRC has a team of full time Clinical Research Coordinators (CRCs) who are GCP-trained to conduct studies in accordance with ICH-GCP guidelines and other regulatory requirements. Our CRCs strive to safeguard the quality, safety and ethical conduct of all clinical studies.
Our CRCs have the following qualifications/certifications: 1) Good Clinical Practice 2) CITI 3) Phlebotomy 4) BCLS
Our team has experience in coordinating trials from Phase I to IV with Principal Investigators (PIs), Sponsors & Contract Research Organisations (CROs) in various disciplines.
The long term continuity of staff is ensured - multidisciplinary knowledge and expertise are maintained and continuously improved.
CRCs with Pharmacy Technician background manages the Investigational Products (IPs). These CRCs are able to perform basic reconstitution of IP (where required). CRCs with nursing background can perform complex blood draws, infusions and injections.
CTRC’s CRC team offers high quality support for both investigator investigated trials and pharmaceutical sponsored trials. If you’re interested in working with CTRC or have any manpower requirement for your research study, please contact us for a further discussion.
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