Senior Medical Data & Safety Review Lead

IQVIA Argentina; Buenos Aires; Presencial; ARS 1.800.000 - 2.400.000; Jornada completa

Descripción de la vacante

IQVIA Argentina seeks an experienced Medical Data Review specialist to oversee medical data review, safety case processing, and related safety activities across clinical trials. The role includes mentoring team members and ensuring medical/scientific plausibility in data reviews.

You will collaborate with Clinical Science and Data Operations on Qlik Sense builds, prepare STAR reports, and contribute to safety data integrity and study-level safety assessments.

Formación

• Medical degree from an accredited medical school.
• Medical license in the country/region of residence.
• 5 years of clinical medicine experience in a clinical or academic setting.
• Minimum of 3 years in Medical Data Review and/or Medical Safety Review.
• Advanced English proficiency.
• Knowledge of MedRA and WhoDrug.
• Experience with Medidata Rave and Inform.
• Experience with Argus Safety.
• Strong Excel, PowerPoint and data visualization skills (Spotfire, J Review, etc.).
• Availability to work in a flexible global schedule.

Responsabilidades

• Review medical data for plausibility and safety assessment.
• Prepare protocol-specific Medical Data Review Plans and STAR reports.
• Define data capture requirements and data listings.
• Collaborate with Clinical Science and Data Operations on Qlik Sense builds and customizations.
• Perform safety reviews of adverse events, meds, labs, and eligibility criteria.
• Prepare and present Safety reviews and MDR summaries.

Conocimientos

Advanced English

Educación

Medical degree

Medical license

Herramientas

Medidata Rave

Inform

Argus Safety

MedRA

WhoDrug

Spotfire

J Review

Excel

PowerPoint

Descripción del empleo

IQVIA Argentina seeks an experienced Medical Data Review specialist to oversee medical data review, safety case processing, and related safety activities across clinical trials. The role includes mentoring team members and ensuring medical/scientific plausibility in data reviews.

You will collaborate with Clinical Science and Data Operations on Qlik Sense builds, prepare STAR reports, and contribute to safety data integrity and study-level safety assessments.