IQVIA is a global leader in leveraging data, technology, and analytics to improve healthcare outcomes. By providing comprehensive solutions in the realm of clinical research, regulatory compliance, and pharmacovigilance, IQVIA helps clients maintain patient safety and meet regulatory demands. This is an opportunity to work with a team that is at the forefront of driving medical advancements and ensuring drug safety worldwide.

Responsibilities

As an Operations Specialist 1 in the pharmacovigilance team, you will:

• Process individual case safety reports (ICSRs) with a focus on quality and compliance.
• Utilize the Argus database for accurate and efficient case management.
• Collaborate with cross-functional teams to support timely case processing and data entry.
• Ensure adherence to standard operating procedures (SOPs) and regulatory requirements.

Qualifications and Requirements

• Experience: 1 – 2 years of hands-on experience in pharmacovigilance, specifically in ICSR case processing.
• Technical Skills: Proficiency in using the Argus database for case management.
• Availability: Only immediate joiners will be considered for this role.

Preferred Skills

• Attention to Detail: High level of accuracy in processing and documentation.
• Communication: Strong written and verbal communication skills.
• Adaptability: Ability to work in a fast-paced, collaborative environment.
• Problem-Solving: Capacity to address challenges and ensure process improvement.

How to Apply

Interested and qualified candidates are encouraged to apply by sending their resumes to dhanalakshmy.tv@iqvia.com.