Project Manager – Clinical Trial Supply Management

Job description

Position: Project Manager – Clinical Trial Supply Management | full-time

Daily Responsibilities:

• Taking full responsibility and accountability for client requests, delivery and opportunities. Communicate/collaborate with clinical CRO, sponsor and clinical study sites to ensure robust supply chain strategies for the on-time delivery of clinical supplies.
• Driving projects towards successful completion while supervising the communication, procurement, logistics, business development, operations, quality and administration abide to regulations and company’s SOP.
• Provide on-going monitoring of inventory and expiration dates for assigned program/study. Ensures alignment with supply forecast and study/program requirements.
• Provide technical oversight of packaging and distribution including, but not limited to document review of packaging specifications, master, executed batch records, distribution instructions, order processing and delivery.
• Support clinical label development process including creation of master label text, translations, and label proofs.
• Ability to read clinical trial protocols and interpret medicine requirements. , create and execute effective clinical trial supply chain solutions, oversight vendor(s) to execute it.
• Write, review, and/or provide input to documents including, but not limited to: pharmacy manuals, INDs, IMPDs, request for proposals, and IRT/IWRS specifications.

  Qualifications:

• Bachelor’s degree or above
• Good coordination ability, self-motivated team player, and detail-oriented
• 2 years of Project Management experience in Drug Supply Chain or clinical research
• Familiar with office software and ERP system
• Good communication skills
• Able to work with flexible hours
• Proficient Chinese-English bilingual. Proficient in Microsoft Office (Excel, Word, PowerPoint)
• Background in pharmacology, Medical and Biology research is preferred