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臨床監(jiān)察員CRAI(Core Team)

1-1.3萬
  • 成都錦江區(qū)
  • 1-3年
  • 本科
  • 全職
  • 招1人

職位描述

藥品臨床監(jiān)查GCP認證Ⅲ期Ⅳ期Ⅰ期Ⅱ期普藥腫瘤藥
工作職責:
1. The Clinical Research Associate (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and
reported in accordance with the protocol, standard operating procedures (SOPs), ICH‐GCP, and all applicable, Regulatory requirements.
2. Implements and monitors local clinical trials to ensure sponsor and investigator obligations are being met and are compliant with applicable local regulatory requirements and ICH‐GCP guidelines
3. Assesses the qualification of potential investigative sites, initiates clinical trials at investigative sites, instructs site personnel on the proper conduct of clinical trials, and close clinical trials at investigative sites
4. Reviews and verifies accuracy of clinical trial data collected, either onsite or remotely
5. Provides regular site status information to team members, trial management, and updates trial management tools
6. Completes monitoring activity documents as required by Company or Sponsor SOPs or other contractual obligations
7. Works closely with other clinical team members to facilitate timely resolution of trial and/or clinical issues
8. Escalates site and trial related issues per Company SOPs, until identified issues are resolved or closed
9. Performs essential document site file reconciliation
10. Performs source document verification and query resolution
11. Assesses IP accountability, dispensation, and compliance at the investigative sites
12. Verifies Serious Adverse Event (SAE) reporting according to trial specifications and relevant local and ICH GCP guidelines
13. Communicates with investigative sites
14. Updates applicable tracking systems
15. Ensures all required training is completed and documented
16. Be assigned logistical support tasks by CTM for Investigator Meetings
任職資格:
1. 1 to 3 years of local trial experience; exposure to MNC and global or Local Phase I -IV trials Clinical research experience
2. Knowledge of ICH and local regulatory authority regulations regarding drug
3. An advanced degree (e.g., M.S., M.B.A., Phar.D., etc.)
職位福利:五險一金、績效獎金、年底雙薪、彈性工作、節(jié)日福利、周末雙休
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工作地點

成都錦江區(qū)百揚大廈(北門)1棟2803-2804室

職位發(fā)布者

顧意蓉/高級人力資源專員

剛剛活躍
立即溝通
公司Logo上??档潞胍磲t(yī)學臨床研究有限公司
康德弘翼(WuXi Clinical),專注于為全球客戶提供覆蓋藥物全生命周期的臨床研究解決方案。聚焦腫瘤與自身免疫性疾病等核心領域,以專業(yè)深度驅動臨床策略落地,助力差異化產品快速推進。服務覆蓋I至IV期臨床,結合專家團隊與智能管理平臺,助力創(chuàng)新療法高效上市,為全球患者帶來更佳治療選擇。
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