Qualifications:
-Bachelor’s degree or above with major in nursing, pharmacy, or other life
science/health care fields
-at least 2 years of field CRA experiences and/or at least 3 years of CRC experiences in international clinical studies; experiences in cardiology studies is a plus; pharmacist license preferred
-substantial understanding of ICH GCP and relevant regulations on execution of clinical trials including CA/EC submission/approval
-experiences of and confidence about CRO management as a sponsor
-good English command
Responsibilities:
-Assist Director of Clinical Operations in management of clinical trials in close collaboration with CRO
-Management and control of study budgets in collaboration with Director of Clinical Operations
-CRO management: being the contact window of CRO, to initiate and hold regular CRO meetings and perform regular accompanied site visits to ensure the trials are on good track and of high quality
-Review and comment MVR of CROs, identify/escalate compliance issues, and develop CAPA if necessary
-May need to enlarge PM functionalitis in case of CRO insufficiency
-Coordination of audit
-Tracking and maintenance of all documentations in TMF
-Ongoing development of company SOP in Clinical Operations
-Regularly visit study sites to establish/maintain business relationship with the investigators to boost patient recruitment