Clinical Trial Associate

Generate:Biomedicines

WorldwideFully remoteFull TimeMid LevelHealthcare & Telemedicine
USD 79,000–103,000 a yearPosted 4h ago

Why we think you can apply

Hiring model
Open worldwide · the employer states no country restriction
Work from
Anywhere, the UAE included

Posted 4 hours ago · apply link checked 11 minutes ago

About the role

Responsibilities

  • Support execution of Phase 3 clinical trials, including site activation, conduct, and closeout
  • Manage TMF setup, maintenance, and QC for inspection-ready documentation
  • Collaborate with CROs on monitoring reports, protocol deviations, and KPIs
  • Coordinate internal teams and vendors to meet Phase 3 regulatory requirements
  • Track timelines, escalate risks, and contribute to mitigation planning
  • Support clinical audit readiness and informed consent and protocol amendment tracking
  • Assist with clinical vendor invoice reconciliation and budget tracking

Requirements

  • Bachelor's degree
  • 2+ years supporting Phase 3 clinical trials at a sponsor or CRO
  • Proficiency in eTMF and CTMS systems
  • Knowledge of FDA and ICH-GCP requirements
  • Proficiency in MS Office (Word, Excel, PowerPoint)
  • Strong organization, attention to detail, and problem solving

Preferred Qualifications

  • Life sciences or related degree
  • Understanding of site management, monitoring, and protocol deviation reporting

Benefits

  • Annual bonus, equity compensation, and competitive benefits package

About the Company

Clinical-stage generative biology company using machine learning to design protein-based medicines. Founded in 2018.

What we look for

  • Bachelor's degree
  • 2+ years supporting Phase 3 clinical trials at a sponsor or CRO
  • Proficiency in eTMF and CTMS systems
  • Knowledge of FDA and ICH-GCP requirements
  • Proficiency in MS Office (Word, Excel, PowerPoint)
  • Strong organization, attention to detail, and problem solving
  • Life sciences or related degree
  • Understanding of site management, monitoring, and protocol deviation reporting
Regulatory ComplianceMicrosoft OfficeGCPMicrosoft ExcelPowerPointClinical TrialsClinical ResearchCTMSeTMF
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