Senior Lead CRA - Hybrid, Cape Town

Placements24

Cape Town

Híbrido

ZAR 900.000 - 1.400.000

Jornada completa

Hace 2 días
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Ventajas ofrecidas por este puesto de trabajo

Hybrid work arrangement
Competitive compensation
Medical insurance
Retirement savings plan
Professional development
Travel reimbursement

Descripción de la vacante

Placements24 is seeking a Lead Clinical Research Associate for a global CRO role based in Cape Town, blending on-site oversight with remote flexibility. You will supervise site monitoring, ensure protocol compliance, mentor junior CRAs, and collaborate with study teams to drive trial execution.

The ideal candidate has 5+ years as a CRA, hands-on ICH-GCP knowledge, strong leadership and communication, and the ability to manage multiple sites in a hybrid work environment.

Formación

  • Bachelor's degree in life sciences or nursing; advanced degree preferred.
  • Minimum 5 years as a Clinical Research Associate with 1–2 years in a Lead CRA or supervisory role.
  • Strong knowledge of ICH-GCP guidelines and local regulatory requirements.
  • Proven ability to conduct remote and on-site monitoring visits.

Responsabilidades

  • Lead site initiation, monitoring, and close-out visits per protocol and ICH-GCP.
  • Ensure accurate data collection and reporting for trials.
  • Verify source data and documentation at investigational sites for accuracy and compliance.
  • Mentor junior CRAs and collaborate with investigators and study teams.
  • Develop study-related documents and monitoring plans; track progress and risks.

Conocimientos

CTMS/EDC
Leadership
Communication
ICH-GCP
Site monitoring
Travel readiness

Educación

Bachelor's degree in life sciences
Advanced degree preferred

Herramientas

CTMS
EDC systems

Descripción del empleo

Placements24 is seeking a Lead Clinical Research Associate for a global CRO role based in Cape Town, blending on-site oversight with remote flexibility. You will supervise site monitoring, ensure protocol compliance, mentor junior CRAs, and collaborate with study teams to drive trial execution.

The ideal candidate has 5+ years as a CRA, hands-on ICH-GCP knowledge, strong leadership and communication, and the ability to manage multiple sites in a hybrid work environment.

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