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Associate Pathology Data Reviewer/Researcher

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Job Details

Job ID:
14003
Category:
Research Scientist
Location:
6 Cedarbrook Dr, Cranbury, NJ
Job Type:
On-site

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

  • Primary duties will be split between report writing/data review and slide shipments/permit applications
  • 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

Qualifications

Experience / Education   

  • 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 

Knowledge / Skills / Abilities:

  • Strong organizational skills with attention to detail are essential
  • Excellent oral and written communication skills in English; ability to speak Chinese is desirable
  • 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

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

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