Pharmacovigilance Associate Position at Teva- Apply before 20th August 2024

Pharmacovigilance Associate I

About Teva

Teva is on a mission to make good health more affordable and accessible, helping millions around the world enjoy healthier lives. With a presence in nearly 60 countries and a rich diversity of nationalities and backgrounds, our team is united by a common purpose. As the world’s leading manufacturer of generic medicines, we are proud to produce many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. We are constantly seeking new ways to make a difference and new people to join us on this journey.

Job Description

• Process serious and non-serious adverse events from various post-marketing sources.
• Ensure accurate and consistent medical coding through MedDRA (Medical Dictionary for Regulatory Activities) for all events in the Safety Database.
• Verify data between source documents and the Safety Database for event/suspect drug coding, seriousness, causality, listedness, and narrative writing.
• Evaluate the need for follow-ups and queries with various stakeholders to ensure correct and accurate data transfer.
• Analyze quality data for trends to prepare the team for process stabilization.
• Provide administrative support by managing assigned case processing activities on a daily basis.
• Coordinate with internal and external stakeholders to obtain necessary information and update the reporting manager on real-time status reports.
• Maintain effective communication with internal departments and external partners, authorities, and vendors to ensure a transparent process.
• Assist in administrative and procedural activities related to the Safety Database as required, ensuring compliance with work instructions and GVP modules.
• Evaluate the quality of case processing and assigned tasks to identify trends for process improvement.
• Meet compliance metrics such as case timelines, assigned trainings, and TAT for assigned activities.
• Provide analytical support for investigations and analysis of trends during audits and inspections.
• Mentor and train new hires in case processing, evaluating their progress during the initial learning phase.

Candidate Profile

• Graduate or Postgraduate in Registered Life Sciences
• Minimum 3 – 4 years of relevant experience
• Extensive knowledge of medical terminology, clinical pharmacology, patient treatment, diagnostic investigations, and pathology
• Sound understanding of pharmacovigilance principles and international regulatory requirements related to drug and patient safety
• Basic knowledge of Teva’s product portfolio, therapeutic area expertise, mechanisms of action, and product/patent safety index
• Excellent communication skills, with professional English speaking, writing, and presentation abilities, and a strong attention to detail

Additional Information

• Experience: 3 – 4 years
• Qualification: Graduate or Postgraduate in Registered Life Sciences
• Location: Bangalore
• Industry Type: Pharma/Healthcare/Clinical Research
• Job Id: 57154
• End Date: 20th August 2024

Join us at Teva and contribute to a healthier world. Apply today!