Clinician (Oncology / Hematology)

micro1·Remote — WorldwideRemotesenior$25,600–$32,000 USD/mo

In short

→Clínico especializado en oncología y hematomatología para monitoreo clínico remoto en compañías estadounidenses.
→Revisión de documentos regulatorios, evaluación de ensayos clínicos y participación en comités médicos (IDMC, DMC).
→Pago de $160–$200/hora en USD con contratación directa a través de micro1, sin visa ni restricciones geográficas.

Fluent written and spoken English required for communication with US teams.

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The questions they'll ask you

1. ¿Cómo evaluarías un evento adverso grave usando CTCAE y qué factores considerarías para su atribución?

🔒 +7 more questions

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💵 USD · Remote · No visa

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What they ask for

✓Especialidad en oncología o hematooncología clínica.
✓Experiencia en evaluación de ensayos clínicos y criterios como RECIST, Lugano, IWCLL, ELN.
✓Habilidad para aplicar CTCAE, análisis de endpoints (PFS, OS, ORR, MRD) y agrupación de eventos adversos.
✓Capacidad para redactar documentos clínicos estructurados y comunicar hallazgos complejos a no especialistas.
✓Experiencia en revisiones regulatorias (CSRs, protocolos, IBs, narrativas de seguridad).
✓Participación activa en comités médicos (IDMC, DMC, adjudicación).

Don't tick every box? That's normal — your free dossier shows your gaps and how to cover them in the interview.

CTCAERECISTLugano CriteriaIMWG CriteriaIWCLL CriteriaELN CriteriaOutcome Endpoint AnalysisDose Escalation AssessmentAdverse Event Grading and AttrRegulatory Document Review

Who should you write to at micro1?

Your free dossier identifies the people who'd interview you — their background, what they value, and how to reach out so you stand out before applying.

Clinician (Oncology / Hematology) via micro1 — remote work with US companies, paid in USD. Pay range: $160–$200/hour USD. 30 openings. High-demand role. Skills: clinical oncology, clinical hematology, clinical trial evaluation, ctcae grading, recist, lugano criteria, imwg criteria, iwcll criteria, eln criteria, outcome endpoint analysis (orr, dor, pfs, os, mrd), dose escalation assessment, adverse event grading and attribution, regulatory document review (csrs, protocols, investigator brochures, safety narratives, dsm/idmc materials), benefit-risk analysis, clinical reasoning, structured written communication, guideline-based documentation, explaining complex information to non-clinical audiences, medical monitoring, committee participation (idmc, dsmb, adjudication, independent review), peer-reviewed publication, attention to detail, critical thinking, problem identification and resolution. micro1 runs a single AI-vetting process (one interview) and matches you with US companies hiring remotely — no visa required, work from anywhere.

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