职位描述
职位描述: KEY ACCOUNTABILITIES? Lead clinical pharmacology outsourcing to support China projectso Maintains a robust and effective relationship with preferred partner CROs in given projects and manages any issues to an effective resolution.o Ensure development and delivery of clinical bioanalytical strategy.o Be responsible for quality aspects by supporting in- and external audit/inspection.? Contribute scientific excellence to China projectso Represent GED/Clinical Pharmacology in China Program/Project Teams.o Contribute to clinical protocol design, operation planning/sampling logistics.o Participate in clinical report and regulatory dossier preparation/review.? Involve in China and pan-Asian R&D strategic discussiono Seek opportunity for innovative early development pathways.o Bring integrated thinking and planning cross disciplines with other China R&D line functions.o Engage in joint China-Japan strategic planning.EDUCATION? PhD or Master’s degree in pharmaceutical, biological or related field with 3-5+ years of post-graduate? experience in the life sciences industry.? Excellent verbal and written communication skills in English.WORK EXPERIENCE? Experience working with a CRO or external partner.? Good understanding of drug discovery and development process, preferably with working experience in GLP and/or GCP.? Prior project management, project coordination, and/or contract and budget management experience.? General understanding of pharmacokinetics, pharmacodynamics, and biomarkers.? Familiar with regulations and guidelines from regional health authorities (e.g. CFDA).? Experience working in global setting with multi-cultural awareness. 职能类别: 生物工程/生物制药 医药技术研发管理人员 关键字: clinical pharmacology biomarker CRO CFDA vendor GLP GCP project