Acepodia just receives its first IND clearance for clinical study in US. More to come in 2020 and 2021. We are looking for talents in clinical operation for this exciting adventure. Share with your resume with us if interested. 【职缺名称】 Clinical Program Associate Manager 临床专案经理 【徵才单位】 Acepodia Biotech Inc. 育世博生物科技股份有限公司 【工作地址】 新北市汐止区新台五路一段99号17楼之7 【工作内容】 ‧ Provides support to Project Team and Clinical Operations Team. ‧ Maintains strong working knowledge of protocols, manuals, and site-facing documents for assigned clinical studies. ‧ Set and enforce project timelines with the assigned study team. ‧ Assists project team in development of site-facing documents, operation manuals, training material, and tools. ‧ Responsible for assuring needs of clinical sites are met by facilitating CRO. ‧ Support site start-up activities and ensure that sites have sufficient project specific supplies. ‧ Participates in site audits, as requested. ‧ Conduct project co-monitoring visits and team training. ‧ Participates and provides support for relevant study meetings, e.g. safety meetings, CRO meetings, medical advisor meetings, and other internal and external meetings. ‧ Proactively identifies, manages, escalates (as needed) and resolves site issues effectively and independently. ‧ Provides support to Project Team and assume additional roles on the team as necessary. ‧ Other duties as assigned by Clinical Operations Manager/Project Manager and per project-specific requirements (i.e. project presentation, project timeline and budget, project bidding, service procurement, etc.). ‧ May be assigned to the project team in the joint project with other departments (e.g. business development, operations) ‧ Job title may be adjusted based applicant experience and skillset 【徵才条件】 #Required Education and Experience ‧ College/University graduate or above (degree in healthcare or life science degree is a plus). ‧ 2 years of monitoring experience gained from a CRO and/or other related clinical research environment. ‧ Experience in clinical patient management, preparing of clinical site-facing documents, and ensuring compliance with protocol and GCP. #Required Knowledge, Skills and Competencies ‧ Strong English language written and verbal communication skills. ‧ Strong interpersonal skills and team player. ‧ Highly organized with exceptional attention to detail. ‧ Computer literacy with high proficiency in MS word and powerpoint. ‧ Interested in working in a start-up environment that is dynamic and fast-paced. ‧ Honest work ethic and shared goal in promoting development of treatments for patients. #Physical Requirements ‧ Minor lifting, < 30 lbs ‧ Must work from Corporate-office location ‧ Regular sitting and keyboard use ‧ May require occasional domestic and/ or international business travel. ‧ Ability to travel up to 10%. ‧ May require occasional international teleconferences 【薪资待遇】 待遇面议 需出差，一年累积时间约三个月以下 员工团保(医疗/寿险/意外险)、公司停车位提供、租屋补助、员工配股、 特休优於劳基法(第一年12天)、14天有薪病假 【联络方式】 赖经理 02-26976100 #13 [email protected] 【其他备注】 Official website: https://www.acepodia.com/ 104: https://www.104.com.tw/job/6ur73?jobsource=company_job --

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