Associate Medical Safety Director — Pharmacovigilance & Risk

IQVIA; Fatih; On-site; TRY 700,000 - 900,000; Full time

Job summary

IQVIA seeks an Associate Medical Safety Director to oversee medical safety activities across post-marketing and trial safety. The role includes medical evaluation of adverse reactions, signal management, and risk assessment, acting as a safety consultant for pharmacovigilance operations.

The position requires medical training, 3+ years of clinical practice with industry experience, and strong ability to synthesize data for internal and external stakeholders.

Qualifications

• Knowledge of safety regulations and guidelines (GCP, regulatory requirements).
• Ability to synthesize data from multiple sources and communicate complex issues.
• Experience in safety signal detection and risk management.

Responsibilities

• Provide aggregate safety reviews to oversee product safety profile.
• Lead signal detection activities and review Signal Detection Reports.
• Contribute to regulatory safety reports (US/EU) and development safety plans.
• Review benefit-risk evaluations for trials and post-marketing studies.
• Support label development and safety updates.

Skills

Signal detection

Aggregate reports

Risk management

Clinical safety review

Stakeholder communication

Education

Medical degree

Job description

IQVIA seeks an Associate Medical Safety Director to oversee medical safety activities across post-marketing and trial safety. The role includes medical evaluation of adverse reactions, signal management, and risk assessment, acting as a safety consultant for pharmacovigilance operations.

The position requires medical training, 3+ years of clinical practice with industry experience, and strong ability to synthesize data for internal and external stakeholders.