上海招聘

• Ability to multiple tasks for 3-5 clinical studies during all phases of protocol execution according to established timelines. 
• Consistently demonstrates initiative and drives performance by contributing to productivity enhancements and continuous improvement by participating in CTA meeting
• Utilizes technology effectively to support the clinical development processes with the use of International Management Package for the Administration of Clinical Trials  （ECLIPSE） of investigative site data.
• Supports project team with ESF document retrieval during HA Sponsor audits.
• Works well with supervision by demonstrating the ability to prioritize work and meet deadlines.
• Exhibits flexibility by being receptive to new systems and processes; willing to enhance current skills to maximize proficiency.
• Effectively coordinates with other departments: GMA, GCR, GRS, CSO, CCE, Finance, GP, as required.
• Communicates effectively using excellent verbal and written skills with both internal and external key stakeholders; coordinates information and document flow to and from both internal and external customers.
• Exhibits professionalism and strong business ethics by maintaining confidentiality where appropriate, exhibiting candor and honesty with co-workers, and respecting Company policies and privileges.
• Presents CTA process updates to other functional areas at appropriate staff meeting venues.
• Demonstrates a strong understanding of the clinical research process and utilizes strong organizational skills to assist with coordination, planning, implementation and administration of projects during all phases of the protocol execution in accordance with established timelines, standard operating procedures and local processes/workflow.
• Interacts effectively with a wide range of individuals and builds professional and collaborative relationships with both external and internal customers to achieve key deliverables and responds proactively to site supply needs. Uses multiple technologies to maintain open and frequent communication with BMS personnel.
• Works well in a team environment with little or no supervision by demonstrating the ability to think in a logical decisive manner and demonstrates a 'can do' approach. Utilizes effective problem-solving approaches and independently follow-up and resolves outstanding issues, within deadline in supporting the efforts of project operations teams.

百时美施贵宝是一家以“研发并提供创新药物，帮助患者战胜严重疾病”为使命的全球性生物制药公司。公司拥有约25000名员工。2016年，百时美施贵宝全球研发投入达近50 亿美元，占全年产品净销售额的28%。

2007年，百时美施贵宝作出了一个重大的战略调整，即向新一代生物制药企业转型。如今，百时美施贵宝将进一步向多元化的特药生物制药企业转型，朝更创新、专业和以患者为中心的方向发展，引领行业新变革。百时美施贵宝将专注于创新药物的研究，以解决肿瘤、免疫肿瘤及肝炎等疾病领域的迫切需求。

在百时美施贵宝，我们为了患者共同努力。作为生物制药行业的引领者，我们致力于为患者提供革新性药物，以治疗最严峻且最具挑战性的疾病，并努力使我们的药物在全球内具有可及性。在为与严重疾病作斗争的患者带来希望的共同信念下，百时美施贵宝以领先的科学发展和创新的产品组合投身于中国市场。

公司于1982年进入中国，于同年成立的中美上海施贵宝制药有限公司是在中国改革开放以后成立的***家中美合资制药企业，目前由百时美施贵宝（中国）投资有限公司、上海医药集团股份有限公司以及国药集团资产管理中心共同投资。

如今，中国已是百时美施贵宝公司全球重要的研发、生产、营销和创新中心之一。百时美施贵宝致力于满足中国未被满足的迫切的重大疾病需求，重点关注于病毒性肝炎和免疫肿瘤两大疾病领域，引领行业发展，开展多元合作，加速提供创新的生物制药产品，以帮助中国患者战胜严重疾病。