Regional Clinical Ops Lead, LATAM (Hybrid)

Psi

Buenos Aires

Híbrido

ARS 100.451.000 - 146.813.000

Jornada completa

Hace 5 días
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Descripción de la vacante

PSI is seeking an experienced Clinical Operations Manager to lead and grow the LATAM Clinical Operations team. This hybrid role is based in Buenos Aires, offering opportunities to mentor staff, optimize resource use, and ensure high-quality trial delivery across the region.

You will collaborate with Project Managers, support audits, and contribute to continuous improvement of quality systems while advancing trials through regulatory inspections and sponsor interactions.

Formación

  • Minimum of 5 years of clinical research experience with people leadership.
  • Onsite CRA experience required.
  • Experience mentoring clinical research professionals in CRO/sponsor environments.
  • Oncology or IBD experience is a plus.
  • Strong communication, organization and problem-solving skills.

Responsabilidades

  • Line manage and develop Clinical Operations staff across levels.
  • Oversee hiring, onboarding, performance management, and development.
  • Coordinate resource allocation and workload planning for trials.
  • Collaborate with PMs and cross-functional teams to deliver studies.
  • Support audits and regulatory inspections; implement quality systems.
  • Assist feasibility assessments and sponsor discussions as needed.

Conocimientos

Team leadership
Staff coaching
English proficiency
Regulatory knowledge
Problem solving

Educación

MD/PharmD/Life sciences degree

Herramientas

ICH-GCP knowledge
Clinical trial systems
Microsoft Office

Descripción del empleo

PSI is seeking an experienced Clinical Operations Manager to lead and grow the LATAM Clinical Operations team. This hybrid role is based in Buenos Aires, offering opportunities to mentor staff, optimize resource use, and ensure high-quality trial delivery across the region.

You will collaborate with Project Managers, support audits, and contribute to continuous improvement of quality systems while advancing trials through regulatory inspections and sponsor interactions.

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