日本真人xxx?69视频,久久久久久久人妻无码中文字幕爆,波多野AV一区二区无码,亚洲av无码之国

臨床監查員CRA(I/II) 15-20k·13薪
北京-朝陽區 1-3年 統招本科
收藏
五險一金 定期體檢 通訊津貼 領導好 發展空間大 公司規模大 彈性工作 崗位晉升 管理規范
avator
王女士 一周前在線 已認證
聊一聊
職位介紹
Duties and Responsibilities (including but not limited to): Adhere with corporate internal polices and requirements, including submission of timesheets and expense reports in a timely manner. Conduct study feasibility and site selection activities Develop and implement innovative approaches for and participates in site recruitment, selection and initiation activities. Assist with investigator meeting activities including organization, preparation and attendance Conduct site management activities including but not limited to site selection visits, site initiation visits, site training, site routine monitoring visits, and site close out visits. Ensure the integrity of clinical data and adherence to applicable regulatory, protocol, and company guidelines. Establish and maintain good rapport with study sites. Write study visits reports and follow up letters within the timeline established by applicable SOPs and guidelines Representation of CRAs during an audit or inspection when assigned Coordinate timely shipment of clinical supplies and study drug to sites. Ensure proper storage, dispensation and accountability of clinical supplies and study drug. Maintain adequate site tracking records Follow up of drug safety issues and safety reports in timely manner, if applicable Communicate site study issues, concerns, and progress to Project Manager, Clinical Team Lead and Clinical Research Manager accordingly Develop and implementation of corrective actions when appropriate Assist with data query form (incl. query process) Prepare /review all patients tracking records Input and maintain study information concerning subject status of financial reimbursement to sites. Conduct and assist with administrative activities as a member of the project team. Education and Work Experience: Bachelor’s Degree in allied health fields: Medical, Nursing, Pharmacy, Psychology, Veterinary or Health Science Minimum of 1 years experience as a Clinical Research Associate Knowledge, Skills, and Abilities: Excellent verbal and written communication skills Good verbal and written English language skills Strong computer literacy e.g. MS word, Excel, PowerPoint, internet Excellent organizational, record retention, and time management skills Knowledge of ICH-GCP, applicable law (local and country) and regulatory requirements
其他信息
語言要求：英語

公司簡介

ICON Clinical Research has a strong reputation in our approaches to clinical development. We apply scientific and operational excellence across all phases of clinical trial outsourcing services for our clients. We work with top pharmaceutical organizations on emerging therapeutic areas ICON provides training and a strong benefits package that include competitive pay, vacation, and additional benefits.
查看全部

獵聘溫馨提示：

1. 如您發現平臺內招聘方存在以下違規行為的，請立即舉報
  • a. 扣押您的身份證件或者其他證件；
  • b. 要求您提供擔保人、擔保金或者以其他名義向您收取財物（ 如培訓費、體檢費、資料費、置裝費、押金等）；
  • c. 強迫您入股或者向您集資；
  • d. 以招聘名義牟取不正當利益；
  • e. 發布虛假招聘廣告信息；
  • f. 工作時長違反勞動法規定；
  • g. 存在其他損害您的合法權益的行為。
2. 如您應聘的崗位屬于涉外勞務合作/海外崗位的，請務必核實招聘方對外勞務合作資質取得情況，同時注意自身資金安全，防范招聘欺詐。
了解更多安全防范知識>
查看全部

猜你喜歡

1 2 3 4