PathAI
PathAI
PathAI ir veselības aprūpes tehnoloģiju uzņēmums, kas izmanto mākslīgo intelektu, lai attīstītu patoloģiju, biomarķieru atklāšanu un zāļu izstrādi. Tā rīki atbalsta biofarmācijas uzņēmumus, patoloģijas laboratorijas un pētniecības organizācijas, uzlabojot laboratoriju darba procesus, digitālo patoloģiju un diagnostisko izpratni. Tādi produkti kā AISight Digital Pathology Image Management System palīdz komandām pārvaldīt un analizēt patoloģijas attēlus precīzijas medicīnas un dzīvības zinātņu pētījumu ietvaros. PathAI strādā 501–1 000 darbinieku, un uzņēmums piedāvā iespējas veselības aprūpes, biotehnoloģiju, datu zinātnes, programmatūras un saistīto jomu profesionāļiem.

Clinical Trial Associate – Massachusetts Remote

Support clinical operations for PathAI’s AI-powered pathology trials as a Clinical Trial Associate. Coordinate laboratory services, investigator sites, specimens, and Clinical Trial Manager deliverables.

Apraksts

  • Monitor clinical trial laboratory services and coordinate with clinical investigator sites
  • Support the lead Clinical Trial Manager (CTM)
  • Apply working knowledge of GCP, ICH guidelines, regulatory requirements, and Title 21 of the Code of Federal Regulations
  • Track and drive the timely resolution of queries assigned to investigator sites and other designated parties
  • Analyze performance trends and provide feedback on investigator sites and the PathAI BioPharma Laboratory
  • Monitor investigators, laboratory performance, study requirements, queries, pending results, and testing turnaround times
  • Partner with data management to investigate and resolve data discrepancies
  • Organize and track stored specimens, including receipt, retrieval, and shipment
  • Coordinate with external vendors and sponsors on laboratory kit delivery and test results
  • Manage routine study activities, including site lists, laboratory manuals, kit orders, specimen reports, PathAI AISight CT Platform case assignments, and pending laboratory analyses
  • Assist with CTM administration, including action tracking, meeting minutes, and process mapping
  • Provide backup CTM coverage for client communications and study management activities
  • Work with cross-functional teams, vendors, Laboratory, Engineering, and support services
  • Coordinate site-level project information and escalate discrepancies
  • Help prepare meeting and training materials
  • Support study start-up deliverables, milestones, project records, and close-out activities
  • Complete additional administrative and process-related duties as required

Prasības

  • At least three years of clinical research experience in medical device and/or pharmaceutical clinical trials
  • Bachelor’s degree in a relevant scientific field
  • Strong organizational abilities
  • High attention to detail
  • Ability to manage multiple tasks simultaneously
  • Experience with digital pathology, radiology, or other imaging technology-based clinical trials is strongly preferred
  • Project management certification is a plus

Priekšrocības

  • Remote work option
  • Relocation benefits are not available for this position

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