Alcon Pharmacovigilance Jobs: Patient Safety Monitor

Welcome to a career opportunity with Alcon, a global leader in eye care, offering a broad spectrum of innovative products. This blog post introduces you to the exciting role of a Patient Safety Monitor within Alcon’s Pharmacovigilance team. Dive into the details about the company, job vacancies, and what it takes to be a part of this dynamic team ensuring the safety and quality of Alcon’s manufactured products.

About the Company

Alcon

Alcon, a Novartis company, is dedicated to enhancing the quality of life by helping people see better. As a global leader in eye care, Alcon develops and manufactures innovative surgical and pharmaceutical products. With a rich history and a commitment to advancing eye health, Alcon stands at the forefront of delivering cutting-edge solutions.

Company Vacancies List

Position Title: Patient Safety Monitor
Company Name: Alcon
Locations: Bangalore, India
Time Type: Full time
Posted on: Posted Yesterday
Job Requisition ID: R-2023-27933

Job Description

Patient Safety Monitor – Key Responsibilities

Case Processing

Process case files according to Standard Operating Procedures (SOP).
Collaborate with affiliate offices to ensure the required dataset is received/requested.
Re-assess data, ensure accurate product selection, and assign required event code(s) in the system.
Complete initial and follow-up reporting assessments.
Respond to Manufacturing Quality Assurance (QA) requests and Health Authority inquiries.
Schedule expedited and periodic regulatory reports based on local and international regulations.

Adherence and Knowledge Maintenance

Adherence to all corporate compliance guidelines and programs.
Maintain a working knowledge of Alcon products, eye anatomy, common diseases, ophthalmic evaluation procedures, safety databases, and reporting tools.
Process and review Surgical – Intra Ocular Lens (IOL) complaint records according to SOPs.
Provide support in reconciliation activities and audit as required.
Evaluate and escalate potential safety issues to management.

Key Performance Indicators

Performance will be measured based on indicators such as meeting internal and external quality standards, timely file reviews and closures, and creating high-quality regulatory reports.

Ideal Background

Education: Graduation in Science (Minimum); Graduation in Optometry/Pharmacy/M. Pharm/B. Pharm/BDS/BAMS/BHMS/Biomedical Engineering/Registered Nurse (Desirable)
Experience: Healthcare professional with 1-2 years of experience (Minimum); Experience in Device Vigilance/Pharmacovigilance/Regulatory Submissions/Clinical Research/PVPI/Medical Coding (Desirable)
Languages: English (written and spoken)

Specific Professional Competencies

Excellent listening ability and communication skills.
Strong decision-making and negotiation skills.
Ability to manage multiple tasks, attention to detail, prioritize work, and manage time effectively.
Knowledge and understanding of national and international medical device regulations and regulatory guidelines.
Basic knowledge of MS Office.