Thermo Fisher Scientific Hiring Safety Reporting Specialist

Thermo Fisher Scientific Inc is the world leader in serving science. Our mission is to enable our customers to make the world healthier, cleaner and safer. With revenues of 13 billion USD, we have approximately 39,000 employees and serve customers within pharmaceutical and biotech companies, hospitals and clinical diagnostic labs, universities, research institutions and government agencies, as well as in environmental and process control industries.

Post : Safety Reporting Specialist

Job Description
The Associate Safety Reporting Specialist assists in the receipt, submission, and subsequent tracking of expedited and periodic safety reports pertaining to the department’s projects. Supports management in producing project metrics as required. Participates in projects and programs relating to safety reporting.

What You'll Do
• Receive, prepare, and submit safety reports to applicable parties, ensuring compliance with regulatory timelines and country legislation.
• Track all expedited/periodic safety report submissions, ensuring retention of evidence of submission. Alert your lead and/or line manager to any quality or timeline issues.
• Develop project management skills by acting as support to an assigned lead, and may also lead small projects.
• Liaise with relevant teams around safety reporting tasks and assist the assigned lead as required.
• Run reports and ensure that repositories/systems are maintained with up-to-date contact information. Provide ad hoc administrative support as and when required.
• Ensure regulatory submission files and filing processes are prepared, set up, maintained, and archived as per the organization's WPDs or applicable client SOPs.
• Assist the manager in the collation of metrics.

Candidate Profile
• Bachelor's degree or equivalent and relevant formal academic / vocational qualification
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years’).

Knowledge, Skills, Abilities
• Basic knowledge of medical terminology
• Good written and verbal communication skills
• Proficiency in Microsoft Office programs and a basic understanding of safety database functionality
• Basic knowledge of procedural documents and working knowledge of global safety reporting requirements (including FDA regulations and guidelines)
• Good organizational and time management skills
• Strong attention to detail and accuracy with orientation toward careful and meticulous work
• Possess the maturity to handle sensitive information and data effectively
• Ability to interact effectively with all levels of the organization
• Ability to work effectively within a team

Additional Information
Experience : 0 to 2 years
Qualification : Bachelor's degree
Location : Hyderabad, Andhra Pradesh
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Clinical Research
End Date : 30th November 2026