Associate Pathology Data Reviewer/Researcher

WuXi AppTecCranbury Township, NJ
14d

About The Position

The Associate Pathology Data Reviewer/Researcher will be responsible for supporting US-based pathologists to ensure an efficient workflow for the pathology portion of studies. This position will require the ability to multi-tasking, excellent organizational skills, and the ability to re-prioritize tasks as needed.

Requirements

  • Bachelor’s degree in health sciences (veterinary science, pharmacology, toxicology) with 3-5 years or more of industry experience
  • Minimum 2 years of GLP laboratory experience
  • Strong organizational skills with attention to detail are essential
  • Excellent oral and written communication skills in English
  • Proficient in Outlook, Word, and Excel, and the ability to quickly learn and master new software applications
  • Ability to multitask and work in a fast-paced, deadline-driven environment

Nice To Haves

  • ability to speak Chinese is desirable

Responsibilities

  • Preparation of reports from templates with information from study protocols and protocol amendments and incorporate significant pathological data (ex. organ weights) per the request of the study pathologist
  • Review and QC standard report data for accuracy and compliance to protocols/protocol amendments/deviations/SOPs
  • Coordinate and monitor the shipment of tissue slides to and from the US for US-based pathologists. This will involve routine communication with our internal Import and Export Department at China (Suzhou) site, multiple shipping vendors, and regulatory agencies (e.g. USDA, USFWS, and US Customs)
  • Apply for re-Export CITES permits to return slides derived from monkey tissue to China, which will include working with shipping vendors/brokers to return slides
  • Coordination of resources for Peer Reviews, such as shipping/receiving slides, data notebook preparation, and on-site facility arrangements
  • Complete an inventory of slides after receiving and before returning
  • Communicating with team members in China (Suzhou) site and ensuring pathology activities follow GLP compliance according to the Test facility SOPs
  • Supporting remote consulting pathologists when applicable
  • Monitoring and tracking Pathologist’s schedules to ensure timely issuance of deliverables
  • Other duties as assigned to meet business needs
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