Remote Clinical Trials Site Activation Lead

Magi-K

Quilmes

Hybrid

ARS 136,310,000 - 227,183,000

Full time

10 days ago

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Job summary

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence. We support the life sciences and healthcare industries to accelerate development and commercialization of medical treatments.

This role directs site activation, maintenance and regulatory activities for studies, partnering with cross regional teams, managing budgets and timelines while ensuring compliance with GCP/ICH and regulatory requirements.

Qualifications

7 years' relevant experience in a scientific or clinical environment including international role.
Strong negotiation and communication skills with ability to challenge.
Excellent interpersonal skills and strong team player.
Thorough understanding of regulated clinical trial environment and drug development.
Proficiency with systems/technology to achieve objectives.
Good regulatory/technical writing skills and knowledge of GCP/ICH.

Responsibilities

Direct and manage site activation, maintenance and regulatory activities for selected studies.
Develop and maintain Management Plans, timelines and budgets per project plan.
Coordinate cross-region collaboration and ensure regulatory compliance across locations.
Provide regulatory and technical support to enable study initiation and maintenance.
Lead and mentor colleagues; track via CTMS and other systems.