426275 SERM Senior Scientist (Open)

Company Overview

At Organization, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. Organization fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success. We’re uniting science, technology, and talent to get ahead of disease together.

Job Summary

Are you passionate about ensuring patient safety and contributing to global health? As a Pharmacovigilance Specialist, you will play a key role in monitoring and managing safety data for clinical trials and marketed products. You’ll collaborate with cross-functional teams to ensure compliance with regulatory requirements and maintain high standards in safety reporting. We value candidates who are detail-oriented, proactive, and committed to delivering quality results in a fast-paced environment.

Responsibilities

• Review and process adverse event (AE) reports from various sources, ensuring accuracy and compliance with defined procedures.
• Interpret medical information, including conditions, lab results, and procedures, to compile clear and complete narrative summaries.
• Ensure proper coding of medical terms and adverse events in the global safety database.
• Prepare and submit reportable cases within regulatory timelines, including expectedness determination.
• Stay updated on case handling standards, regulatory guidelines, and database technologies.
• Collaborate with teams to maintain and improve safety database systems and processes.

Qualifications

• Bachelor’s degree in Life Sciences, Pharmacy, or a related field.
• Strong understanding of pharmacovigilance principles and regulatory requirements.
• Excellent analytical and problem-solving skills.
• Detail-oriented with a commitment to quality and accuracy.
• Proficient in medical terminology and coding.
• Strong communication and collaboration skills.
• Ability to work effectively in a fast-paced environment.

Experience

• Minimum of 3-5 years of experience in pharmacovigilance or related field.

Environment

• Hybrid work mode, combining both in-office and remote work.
• Job location: Bengaluru Luxor North Tower.

Salary

• Estimated salary range: 4,000,000.

Growth Opportunities

• Opportunities for career advancement within the organization, including potential leadership roles in pharmacovigilance and safety management.

Benefits

• Comprehensive health insurance.
• Paid leave and flexible work policies.