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Safety Administrator

2+ years
Not Disclosed
10 Aug. 29, 2025
Job Description
Job Type: Remote Education: Bachelor's degree preferred (scientific, healthcare, or administrative field) Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title

Safety Administrator


Location

  • Fully Remote (Available in 2 locations)

  • India (one of the listed locations)

Job ID

R-01324589

Job Type

Full-time

Category

Clinical Research

Work Schedule

Standard (Monday to Friday)

Work Environment

Remote (Office-based setup)


Company Overview

At Thermo Fisher Scientific, through our PPD® clinical research services, we help bring life-saving therapies to market faster. As a leading global contract research organization (CRO), our teams combine deep scientific knowledge with clinical excellence to support global trials in 100+ countries. Join us in our mission to make the world healthier, cleaner, and safer.


Position Summary

Reporting to the Pharmacovigilance (PV) Manager, the Safety Administrator (SA) provides administrative support to the Global Safety Writing Team. This team is responsible for delivering critical safety documents such as:

  • Aggregate Safety Reports

  • Risk Management Plans (RMPs)

  • Responses to Regulatory Authority Assessments

The Safety Administrator ensures timely and accurate document support, efficient coordination of team resources, and maintenance of compliance metrics.


Key Responsibilities

Document Support & Preparation

  • Assist safety writers in the preparation of deliverables by:

    • Drafting planning documents

    • Compiling and formatting final reports

    • Supporting data request preparation

    • Filing and archiving documents as per SOPs

Team & Project Coordination

  • Manage the team’s shared mailbox and respond to queries or escalate appropriately.

  • Track team- and project-related data (e.g., deadlines, document status).

  • Schedule internal and client meetings as needed.

Compliance & Reporting

  • Generate and maintain compliance metrics for safety documentation.

  • Ensure adherence to deadlines and internal quality standards.


Qualifications

Education & Experience

  • Bachelor's degree preferred (scientific, healthcare, or administrative field)

  • Prior experience in pharmacovigilance or clinical research preferred

Skills & Competencies

  • Strong organizational skills with the ability to manage multiple priorities

  • Excellent attention to detail

  • Ability to work effectively under tight deadlines

  • Proficient in Microsoft Office, especially Word and Excel

  • Strong written and spoken English

  • Effective oral and written communication

  • Comfortable working both independently and as part of a remote team

  • Proactive and adaptable in a fast-paced and evolving environment

  • Proficient keyboard and typing skills


Ideal Candidate Attributes

  • Self-starter with a positive, can-do attitude

  • Able to thrive under pressure while maintaining high accuracy

  • Comfortable working across time zones and communicating virtually

  • Eager to contribute to a high-performing, global safety team


Why Join Us

At Thermo Fisher Scientific, you’ll be part of a global team that values:

  • Integrity, Intensity, Innovation, and Involvement

  • Continuous learning and development

  • A collaborative culture with opportunities for career advancement

  • A meaningful mission to improve health outcomes worldwide


Apply Now and become part of a company where your work truly matters.