Remote Clinical Data Manager: Lead & Develop Study Teams

Worldwide Clinical Trials

Quilmes

A distancia

ARS 900.000 - 1.300.000

Jornada completa

Hace 6 días
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Descripción de la vacante

IQVIA is seeking a Clinical Operations Manager in Buenos Aires to lead a team of clinical staff supporting multiple studies. You will ensure proper resourcing, training, and adherence to project objectives, while guiding performance and staff development.

Ideal candidates have a degree in science/healthcare, clinical trial experience, and strong knowledge of GCP/ICH guidelines, with excellent communication and time-management skills. On-site role based in Buenos Aires, Argentina.

Formación

  • Bachelor's Degree in scientific discipline or health care preferred.
  • Prior clinical trial experience including management/leadership responsibilities.
  • Knowledge of GCP and ICH guidelines.

Responsabilidades

  • Manage staff in accordance with organizational policies and regulations.
  • Plan, assign, and direct work; assess performance and develop staff.
  • Oversee training plans, SOP reviews, and training experiences.
  • Allocate resources to clinical studies and assign staff accordingly.
  • Monitor quality of staff work and implement corrective actions as needed.
  • Collaborate with clinical teams and leadership to address challenges and deliver client service.
  • Participate in quality initiatives and process improvements.

Conocimientos

Leadership
Project management
Regulatory knowledge
English proficiency
Communication
Time management
Relationship building

Educación

Bachelor's degree in scientific discipline or healthcare

Herramientas

Microsoft Word
Microsoft Excel
PowerPoint

Descripción del empleo

IQVIA is seeking a Clinical Operations Manager in Buenos Aires to lead a team of clinical staff supporting multiple studies. You will ensure proper resourcing, training, and adherence to project objectives, while guiding performance and staff development.

Ideal candidates have a degree in science/healthcare, clinical trial experience, and strong knowledge of GCP/ICH guidelines, with excellent communication and time-management skills. On-site role based in Buenos Aires, Argentina.

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