responsibilities, including: meetings with necessary project team members, reporting activities, exploratory analyses/graphics, and additional analyses to support publications for individual clinical trials/studies/projects. Is able to support program-wide strategic analyses, including Health Authority responses;...
• University Degree or Equivalent preferably in a medical/science-related field. • Prior work experience demonstrating knowledge and understanding of clinical trials. • Previous experience managing projects is desirable. Skills, Experience and Competencies: ...
• Work experience in life sciences or medically related field, including biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company 职位要求 学历要求:本科及以上 工作经验:经验不限 外语要求:英语 公司福利 "Flexible Working Time ...
18. Actively contributes to process improvement; training and mentoring of Clinical Trial Administrators, Site Managers and other LTMs. ADDITIONAL RESPONISIBILITIES: 1.Prepares country specific informed consent in accordance with GCO procedural document/templates. Reviews and manages site specific informed ...