• Role Overview: Patient Safety Monitor
• Key Responsibilities
• Role Dimensions
• Key Performance Indicators (KPIs)
• Qualifications and Experience
• Language Requirement
• Professional Competencies
• Apply online

Pharmacovigilance Job Opportunities in Bangalore: Become a Patient Safety Monitor

Are you a healthcare professional with a passion for ensuring patient safety within the pharmaceutical industry? Look no further! Exciting opportunities await you as a Patient Safety Monitor in Bangalore, India. Alcon, a leading global medical company, is seeking dedicated individuals to join their team in this critical role. Let’s delve into the details of this enticing position that plays a vital role in maintaining the integrity and safety of pharmaceutical products.

In the ever-evolving field of healthcare, patient safety is paramount. Alcon, a subsidiary of Novartis, is a global leader in providing innovative eye care products and solutions. As a Patient Safety Monitor, you will contribute to the company’s commitment to maintaining the highest standards of safety for patients worldwide.

Role Overview: Patient Safety Monitor

As a Patient Safety Monitor, you will take on a crucial role in ensuring the safety of patients using Alcon’s products. This role involves meticulous case processing and adherence to Standard Operating Procedures (SOPs) to accurately report adverse events and product complaints. Your attention to detail, communication skills, and knowledge of medical regulations will contribute to the overall safety and quality of Alcon’s products.

Key Responsibilities

Your responsibilities as a Patient Safety Monitor will encompass a variety of crucial tasks:

• Processing case files according to SOPs.
• Collaborating with affiliate offices to ensure accurate data collection.
• Reassessing data, ensuring precise product selection, and assigning event codes.
• Completing initial and follow-up reporting assessments.
• Responding to Manufacturing Quality Assurance (QA) requests and Health Authority inquiries.
• Launching quality investigation records.
• Scheduling expedited and periodic regulatory reports.
• Reviewing Surgical – Intra Ocular Lens (IOL) complaint records.
• Supporting reconciliation activities and audits.
• Evaluating and escalating potential safety issues.
• Adhering to corporate compliance guidelines and programs.

Role Dimensions

• Number of Associates: None
• Financial Responsibility: None
• Impact on the Organization: Low

Key Performance Indicators (KPIs)

Your performance will be evaluated based on various KPIs, including:

• Meeting internal and external quality standards.
• Reviewing and closing files within prescribed timelines.
• Creating high-quality regulatory reports before assigned due dates.

Qualifications and Experience

• Education:
  • Minimum: Graduation in Science
  • Desirable: Graduation in Optometry, Pharm-D, M. Pharm, BDS, BAMS, BHMS
• Experience Requirement:
  • Minimum: Healthcare professional with 0-2 years of experience
  • Desirable: 0-2 years of experience in Device Vigilance / Pharmacovigilance / Regulatory Submissions / Clinical Research / PVPI / Medical Coding.

Language Requirement

• Minimum: Proficiency in English (written and spoken)

Professional Competencies

• Excellent listening and communication skills.
• Strong decision-making and negotiation abilities.
• Effective multitasking, attention to detail, and time management.
• Knowledge of national and international medical device regulations and guidelines.
• Understanding of medical aspects of medical device safety and vigilance.
• Basic knowledge of MS Office.

Apply online