
Clinical Trial Associate
Generate:Biomedicines
WorldwideFully remoteFull TimeMid LevelHealthcare & Telemedicine
USD 79,000–103,000 a yearPosted 4 hours ago4h agoApply link checked 11 minutes 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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Generate:Biomedicines
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