廣告
Clinical Trial Liaison , Oncology, Taiwan
Free
Clinical Trial Liaison , Oncology, Taiwan
Taiwan, Taiwan, Taiwan,
發表 November 15, 2023
描述
Duties and Responsibilities:Provide country/regional operational insight into site feasibility and selection and overall patient recruitment strategyParticipate in Clinical Study Team Meetings and Quality Review Meetings where necessary providing input to study teams on operational issues based on site visits and contactsAttend and present at investigator meetings, monitor workshops/trainingParticipate in site visits with investigator site staff and/or CRO representatives, or independently, in support of clinical trial execution and report back to study teams e.g. feasibility, startup activities, enrolment or escalated study/site issuesResponsible for review, documentation and follow up of investigator site issues including tracking metricsProvides sponsor regional operational support and acts as point of escalation for investigator sites as appropriateParticipate in Regulatory GCP inspections and/or audits at investigator sites as sponsor representativeComplete all administrative responsibilities consistent with SOPs and departmental guidelines including but not limited to required training, field activity documentation, expense reporting, and other assigned tasksManage travel and local expenses in accordance with sponsor and TMAC policiesQualifications and Experience:Minimum Bachelor’s degree, master’s preferred or terminal degree (MD, PhD or PharmD)8+ years relevant industry and/or CRO experience requiredExtensive experience in global clinical trial operations requiredOncology clinical trial experience preferredExtensive medical and scientific knowledge and clinical development understandingExcellent communicator of technical and scientific informationExcellent interpersonal skills and demonstrated collaborative as well as independent working styleAbility to build relations with the external medical communityProactive and self-motivated, ability to align activities with the clinical development plans (CDPs)Strong organizational skills with effective use of time and prioritizationCross cultural awarenessFluency in English and in local language in country of residence requiredA working knowledge of ICH/GCPComputer skills including Excel, Word, and PowerPoint A willingness to travel frequently within assigned geographical territory, including overnight travel. Valid driver’s license