Clinical Trial Material Specialist (thời vụ 6 tháng)

☞ Zuellig Pharma Viet Nam

전망: 159

갱신일: 04-05-2024

위치: Ho Chi Minh

범주: 제약 / 화학 / 바이오 테크 식음료

수평: Trưởng nhóm / Giám sát

봉급: Cạnh tranh

교육: Đại học

경험: 4 - 7 Năm

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업무 설명서

Working location: Tan Tao Industrial Park, Binh Tan

MAIN TASK
• Identifying new sales leads
• Pitching services including comparator sourcing, CTM studies…
• Maintaining fruitful relationships with existing clients.
• Developing quotes and proposals
• Managing and coordinating cross-functional project teams
• Serving as the primary project contact with the Clients including Sponsor,CRO,....
• Monitoring team performance against contract, customer expectations, and project baselines
• Composing the Depot Project Instruction, Letter of Authorization…
• Preparing the CTM budget, mornitoring and charging cost to Clients & SSG.
• Supervising the CTM operator the monthly report.
• Leading problem solving and resolution efforts to include management of risk, contingencies and issue resolution
• Developing study management plans, together with team assignments and accountabilities and oversight of database maintenance
• Ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures.
SUB-TASK
• Other tasks are assigned by Director and Whs Manager
• Supervising routine CTM activities and projects
• Reviews and analyzes reports, records and directives, and confers with managers/supervisors to obtain data required for planning activities, such as new commitments, status of work in progress, and
problems encounter

작업 요구 사항

• A Bachelors degree or equivalent in pharmacy.
• Ideally seven years clinical research experience with four years project management experience
• Alternatively, you should have an equivalent combination of education, training and experience
• Good in written, speaking and listening English Excellent oral and written communication
• Proficiency in MS Office suite, including Word, Excel, and PowerPoint.