IQVIA Fresher Pharmacovigilance Hiring | Safety Aggregate Report Coordinator | Kolkata

IQVIA Fresher Pharmacovigilance Hiring for Safety Aggregate Report Coordinator

Embark on a rewarding journey with IQVIA, a global leader in clinical research and healthcare intelligence, as they open opportunities for freshers to join their Safety Aggregate Reporting and Analytics (SARA) services team in Kolkata, India.

Role Overview: Safety Aggregate Report Coordinator at IQVIA

Job Location: Kolkata, India

Employment Type: Full-Time

Experience Required: Fresher to 2 years

As a Safety Aggregate Report Coordinator, you’ll manage administrative and operational tasks crucial to IQVIA’s pharmacovigilance and safety reporting processes. This role is perfect for those passionate about drug safety and eager to contribute to healthcare advancements.

Key Responsibilities

• Schedule and attend planning meetings and maintain the minutes of the meeting. Initiate and manage the workflow of controlled documents.
• Under direction of Functional Project Leads, set-up & maintain SARA services trackers for new projects, and enter, update and maintain SARA/ BRM / LR deliverables schedules for project in the designated trackers.
• Assist with metrics management, reconciliation, audit and training tasks, monitor SARA specific mailboxes and other coordinator activities as assigned.
• Prepare final formatting/compilation of document(s) including necessary attachments/appendices.
• May assist with creating project tracking spreadsheets and associated tracking entry specifications
• Assisting in database validation through performance of user testing
• Performing ad hoc database searches
• Escalating any system/equipment problem.
• Oversee and co-ordinate administrative support by coordinating team/department/customer/project oversight group meetings & disseminating/saving meeting minutes, coordinating stationery orders, dispatching documents via courier services, reserving meeting rooms and IT equipment and providing administrative support where required.
• Update, maintain and organize applicable electronic file systems and SARA Sharepoint sites.
• Contribute to achievement of departmental goals e.g. utilization realization and productivity metrics.
• Read and acknowledge all necessary IQVIA standard operating procedures (SOPs) and customer SOPs as required. Ensure all required training is executed in a timely fashion and documented ensuring Good Documentation Practices (GDP).
• Support and/or contribute to technology / innovation activities.

Qualifications and Skills

Educational Requirements

• Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or a related field.

Skills & Competencies

• Technical Proficiency:
  • Familiarity with Microsoft Office tools (Word, Excel, PowerPoint).
  • Basic knowledge of medical terminology and pharmacovigilance processes.
• Soft Skills:
  • Strong organizational and time management abilities.
  • Excellent communication skills, both written and verbal.
  • Self-motivation and flexibility to adapt to dynamic project requirements.
• Experience:
  • Freshers or candidates with up to 2 years of experience in drug safety, literature surveillance, or related fields.

H4: How to Apply

Eager to start your career in pharmacovigilance? Apply today to join IQVIA as a Safety Aggregate Report Coordinator.

👉 Click Here to Apply

Tagged as: Good Clinical Practice (GCP), Pharmaceutical Careers, Pharmacology