Remote Associate Medical Director, Psychiatry - Argentina

IQVIA LLC

Buenos Aires

Híbrido

ARS 106.678.000 - 182.877.000

Jornada completa

Hace 5 días
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Descripción de la vacante

IQVIA LLC is seeking an Associate Medical Director (Psychiatry) to provide medical leadership for clinical trials from a home-based base in Argentina. The role supports sites, reviews protocols and safety data, and may serve as a regional advisor on assigned projects.

The ideal candidate holds a Medical Degree with Psychiatry board certification, excellent English, and 3–5 years of trial experience in pharma or CRO. Occasional international travel is expected.

Formación

  • Medical degree from an accredited medical school.
  • Psychiatry board certification is mandatory.
  • Advanced English level in writing and speaking.
  • 3–5 years of experience supporting clinical trials in Pharma or CRO.
  • Current medical license in country/region of residence.

Responsabilidades

  • Serve as backup Medical Advisor and may act as Regional Medical Advisor on projects.
  • Provide medical support to investigative sites and project staff for protocol-related issues.
  • Contribute to medical reviews of protocols, IDB, and CRFs as needed.
  • Deliver therapeutic area training to project teams and attend Investigator Meetings.
  • Review trial-related Adverse Events and collaborate with Pharmacovigilance on SAE reviews.
  • Participate in CSR reviews and patient narratives; respond to urgent protocol issues 24/7.

Conocimientos

Clinical trials experience
Spanish & English communication
Attention to detail

Educación

Medical degree
Psychiatry board certification

Descripción del empleo

IQVIA LLC is seeking an Associate Medical Director (Psychiatry) to provide medical leadership for clinical trials from a home-based base in Argentina. The role supports sites, reviews protocols and safety data, and may serve as a regional advisor on assigned projects.

The ideal candidate holds a Medical Degree with Psychiatry board certification, excellent English, and 3–5 years of trial experience in pharma or CRO. Occasional international travel is expected.

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