423427 Senior Literature Specialist III (Open)

Job Summary

The Senior Literature Specialist III will provide essential support for Global Safety literature screening activities, focusing on Individual Case Safety Reports (ICSR) and signal detection in compliance with established procedures and regulatory requirements. This role is critical in ensuring the timely production of key deliverables and contributes to the organization's pharmacovigilance efforts.

Responsibilities

• Screen and review literature search results (articles, abstracts, citations) for ICSR identification.
• Triage literature search results to identify potential articles of interest with relevant safety information for signal detection and periodic reporting.
• Demonstrate proficiency in search strategy activities for literature surveillance.
• Conduct quality checks on literature articles triaged by junior team members.
• Develop and share knowledge and experience in pharmacovigilance and literature surveillance with the team.
• Collaborate with team members to recognize and resolve potential issues.
• Participate in continuous process improvement activities related to the area of responsibility.

Qualifications

• Education: Bachelor's degree in a relevant field (e.g., Life Sciences, Pharmacy).
• Experience: Pharmaceutical industry experience, particularly in drug safety, regulatory, clinical development, or medical affairs.
• Knowledge: Working knowledge of key pharmacovigilance regulations and methodologies.
• Language Skills: Proficient in English, with strong written and verbal communication skills, especially in scientific and medical terminology.
• Analytical Skills: Ability to evaluate data and draw conclusions with guidance from senior team members.
• Attention to Detail: Strong focus on detail and accuracy in work.
• Interpersonal Skills: Highly developed interpersonal, presentation, and communication skills.
• Technical Skills: Proficient in computer and IT skills, with the ability to work with web-based applications.

Preferred Skills

• Experience in signal detection and periodic reporting processes.
• Familiarity with advanced literature search techniques and tools.

Experience

• Minimum of 3-5 years of relevant experience in the pharmaceutical industry, particularly in drug safety or pharmacovigilance.

Environment

• Work Type: Full-time
• Work Mode: Hybrid
• Location: Bengaluru Luxor North Tower

Salary

• Estimated Salary Range: ₹4,000,000

Growth Opportunities

• Opportunities for career advancement within the organization, particularly in pharmacovigilance and regulatory affairs.

Benefits

• Comprehensive benefits package including health insurance, paid leave, and flexible work policies.