Pharmacovigilance Specialist

We are seeking Pharmacovigilance Specialists to join our team for an upcoming project with a global pharmaceutical company. The ideal candidates should bring at least one year of experience in Pharmacovigilance and have a solid understanding or hands-on experience with Individual Case Safety Report (ICSR) submissions.

Key Responsibilities:

• Perform and manage Pharmacovigilance activities, including the review and analysis of safety data.
• Handle Individual Case Safety Reports (ICSRs) and ensure accurate and timely submissions.
• Collaborate with cross-functional teams to maintain compliance with regulatory requirements.
• Contribute to maintaining high standards of patient safety and data quality.

Qualifications:

• Minimum of 1 year of experience in Pharmacovigilance.
• Knowledge or experience with Individual Case Safety Report (ICSR) submissions.
• Strong understanding of Pharmacovigilance processes and regulatory requirements.
• Excellent organizational skills and attention to detail.

Additional Information:

• Start Date: August 15th
• Workload: 35-40 foreign cases per day, with potential for local cases.
• Environment: Fast-paced and dynamic setting within a leading global pharmaceutical company.

If you meet these qualifications and are interested in a challenging and rewarding role, please apply or reach out to discuss further.