Remote Site Activation Lead – ICF & Regulatory (LATAM)

Eng

Buenos Aires

A distancia

ARS 61.816.000 - 108.178.000

Jornada completa

Hace 5 días
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Descripción de la vacante

IQVIA is seeking a Site Activation Specialist, ICF Lead to manage country-level start-up activities within LATAM, operating in a homebased role. You will serve as SPOC for studies, ensuring regulatory compliance, documentation readiness, and timely milestones across sites and teams.

The role requires a Life Sciences degree and at least 3 years in clinical research or related fields, with strong communication and multitasking abilities to drive start-up success.

Formación

  • Bachelor's degree in Life Sciences or related field is required.
  • Minimum 3 years of clinical research or equivalent experience.
  • Experience with country-specific regulatory requirements in LATAM regions.
  • Strong communication, organizational skills and problem-solving mindset.
  • Ability to manage multiple priorities and work cross-functionally.

Responsabilidades

  • Serve as SPOC for assigned studies, coordinating with sites and project teams.
  • Ensure compliance with local regulations, SOPs and timelines.
  • Lead feasibility, site identification, start-up and activation activities.
  • Prepare and review site documentation for accuracy and timeliness.
  • Maintain accurate data in internal systems and tracking tools.
  • Provide regulatory and operational expertise to SAMs during start-up and execution.
  • Perform quality control reviews of documentation from sites.

Conocimientos

Communication
Attention to detail
Problem-solving mindset
Multitasking

Educación

Bachelor's degree in Life Sciences or related field

Descripción del empleo

IQVIA is seeking a Site Activation Specialist, ICF Lead to manage country-level start-up activities within LATAM, operating in a homebased role. You will serve as SPOC for studies, ensuring regulatory compliance, documentation readiness, and timely milestones across sites and teams.

The role requires a Life Sciences degree and at least 3 years in clinical research or related fields, with strong communication and multitasking abilities to drive start-up success.

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