Safety Reporting Coordinator at Thermo Fisher Scientific provides administrative support to the Pharmacovigilance department, managing safety report submissions, filing, tracking, and archiving across clinical trials. The role involves coordinating with multiple departments, maintaining organizational systems, and may include training staff on safety reporting processes.

Responsibilities

Submit safety reports to applicable parties with scanning, indexing, filing, and archiving per SOPs

Extract and collate reporting information via Clinical Trial Management System and maintain contact lists

Provide administrative support on audit readiness, meetings, filing, and system updates





Train Pharmacovigilance department staff on safety reporting processes and organizational systems

Coordinate study file distribution to clients and assist with file reviews and in office audits

Requirements

Bachelor's Degree or equivalent formal academic/vocational qualification

Minimum 2 years of relevant experience in comparable role

Proficiency in Microsoft Office (Word, Excel, PowerPoint, Access)

Excellent written and verbal communication skills

Strong attention to detail and organizational abilities

Ability to manage multiple tasks and handle stress effectively

📌 Safety Officer (2 years relevant experience required) (Andhra Pradesh)
🏢 Thermo Fisher Scientific
📍 Andhra Pradesh