The CRC supports the Sr. CRS in facilitation and administrative support to clinical trials being proposed to CTU of TMCC. These activities include distribution, collection, and checking for completion of Confidentiality Disclosure Agreement (CDA) and Feasability Questionnaires (FQ) provided by sponsoring Pharma, Biotech, or CRO companies. Collaboration/coordination with study team of Investigator and Study Coordinator on study requirements including study supplies, laboratory request procedures, facilitation of funds with the foundation and quality check for protocol submission to IRB. Clinical Research Coordinator or CRC will be the back-up point person of the Sr. CRC and delegated the responsible for coordination with the sponsor as well as the study team to ensure quality and timely provision, distribution, completion, and submission of CDA&aposs and FQ&aposs. CRC also liases the parties involved in the contracting process to ensure timely CTA review and approval process by Legal department and coordinates with IRB Associates on review and approval of protocol propsals as well as the Pharmacy department for Investigational Product management/storage. CRC also supports as a communication line between sponsor representative and the study team on issues related to the administrative needs of the study during its implementation. Job qualifications Graduate of Medical Technologist, Pharmacist, Nursing or Allied Medical Course Good communication skills, both oral and written Computer literate (MS Office) Preferably with PRC License Show more Show less