job title: Analyst - R&D (Elanco)

Roles and Responsibilities

Your Responsibilities: -

• Responsible for data entry, seriousness assessment and causality assessment of adverse event reports in the PV database

• Identifies issues in case processing that may result in a delay in submission and escalates issues to management as appropriate.

• Develop an understanding of pharmacovigilance regulations.

• Comply with internal and external timelines for managing adverse events and product complaint case processing and case submission processes as appropriate.

What You Need to Succeed (minimum qualifications):

• Bachelor’s or master’s degree in related field.

• 0-1 year of experience in Basic knowledge of medical terminologies and able to understand common medical terms relevant to pharmacovigilance and adverse event reporting.

What will give you a competitive edge (preferred qualifications):

• Effective verbal and written communication skills to liaise with internal and external stakeholders.

• Ability to work effectively on multiple products and effectively manage priorities.

• Ability to establish and maintain effective working relationships with coworkers, managers and relevant stake holders.

• Capable of adhering to applicable, global, local regulatory requirements.

Additional Information:

• Travel: 0%

• Location: India, Bangalore