北京招聘

  

Major Responsibilities

  

Assists Clinical Operations Manager to manage clinical studies or leads clinical studies independently, if required

  

• Assists Clinical Operations Manager (COM) or leads independently (COM II) to plan, organize, and manage all aspects of assigned clinical trial(s)

• Assists COM or leads independently to manage the efforts of all key functional departments to perform all project-related activities according to project milestones/timelines or leads (ACOM II) these activities, if required.

    

Performs Quality Oversight Visit (QOV)

  

• Prepares QOV by being familiar with study protocol, plans, previous monitoring reports, follow-up letters, etc.

• Conducts on-site QOV

• Completes QOV reports

• Follows-up with CROs and relevant parties for actions/ resolutions for issues identified through the QoVs

• Prepares “lessons learnt” document and shares with the clinical operations team after the QoVs

          

 

  

Qualification

  

• Bachelor’s level degree or above in life sciences, pharmacy, nursing or medical

• 4 years or more years of clinical research experience in the Pharmaceutical, CRO or relevant filed

• Excellent communication and interpersonal skills

• Excellent organizational skills and ability to prioritize and multi-task

• Fluent in English (writing and speaking)

          

 

  

百济神州是一家立足于科学的全球性生物科技公司，专注于开发创新、可负担的药物，旨在为全球患者改善治疗效果，提高药物可及性。目前公司广泛的药物组合包括40多款临床候选药物。公司通过加强自主研发能力和合作，加速推进多元、创新的药物管线开发。我们致力于在2030年前为全球20多亿人全面改善药物可及性。百济神州在全球五大洲打造了一支超过8,000人的团队。