Pharmacovigilance Associate

Job description:

They are responsible for processing and evaluating adverse event reports for marketed and investigational products. This role ensures compliance with regulatory requirements and internal timelines while maintaining accuracy and completeness in case management.

Key Responsibilities:

• Receive, triage, and process adverse event reports from various sources.
• Evaluate clinical trial, post-marketing, and solicited reports for completeness and accuracy.
• Conduct duplicate searches, data entry, and assign cases to specialists.
• Assess seriousness, expectedness, and validity of adverse events.
• Prioritize workload to meet company and regulatory deadlines.
• Communicate with partners, affiliates, and stakeholders as needed.

Qualifications:

• Bachelor’s degree in a scientific or medical field required.
• Experience with data coding and database management preferred.
• Knowledge of medical terminology and pharmacovigilance practices.
• Remote East coast only.
• Strong attention to detail, multitasking ability, and communication skills.
• Less than 06 years experience in Product Safety/Pharmacovigilance is required