Senior Oncology CRA – Remote Lead, Phase II–III Trials

Piper Companies

United States

A distancia

USD 90.000 - 140.000

Jornada completa

14 días+

Una candidatura completa en un minuto

Currículum y carta de presentación personalizados, listos para enviar.

Supera los filtros ATS

Ventajas ofrecidas por este puesto de trabajo

Medical insurance
Dental coverage
Vision insurance
Retirement plans
Remote work flexibility

Descripción de la vacante

Piper Companies is actively seeking a Senior Clinical Research Associate (CRA) to support late-phase oncology trials within the biotech industry. The Senior CRA role suits professionals who thrive in a fast-paced environment and bring a hands-on, relationship-driven approach to site monitoring and trial execution.

Responsibilities include overseeing Phase II–III oncology studies with ICH-GCP compliance, conducting on-site visits (~8 days/month), and ensuring high-quality, audit-ready data

Formación

  • Senior CRA with oncology trial experience.
  • Proven expertise in independent monitoring and full lifecycle oversight.

Responsabilidades

  • Oversee Phase II–III oncology studies per ICH-GCP and protocols.
  • Perform on-site monitoring visits and site initiation/close-out activities.
  • Conduct source data verification and CRF assessments for audit-ready data.
  • Build partnerships with investigative sites to drive enrollment and resolve operational challenges.
  • Identify site risks and ensure milestones stay on track.

Conocimientos

ICH-GCP compliance
On-site monitoring
Study oversight
Clinical trial management
Site relationship management
Data verification
Multi-site management

Descripción del empleo

Piper Companies is actively seeking a Senior Clinical Research Associate (CRA) to support late-phase oncology trials within the biotech industry. The Senior CRA role suits professionals who thrive in a fast-paced environment and bring a hands-on, relationship-driven approach to site monitoring and trial execution.

Responsibilities include overseeing Phase II–III oncology studies with ICH-GCP compliance, conducting on-site visits (~8 days/month), and ensuring high-quality, audit-ready data

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