Instagram
youtube
Facebook

Safety Administrator

0-2 years
₹4.5 – ₹6.5 LPA
10 Aug. 8, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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: Remote (Available in 2 locations)
Job Type: Full Time
Category: Clinical Research
Work Schedule: Monday to Friday
Environment: Office (Remote Setup)
Estimated Salary: ₹4.5 – ₹6.5 LPA (based on industry standards for entry-to-mid level pharmacovigilance support roles in India)

Job Description:

Join our dedicated Clinical Research Services team, a crucial part of our global CRO (Contract Research Organization), committed to advancing life-saving therapies. As a Safety Administrator, you will report to the Pharmacovigilance (PV) Manager and provide essential administrative support to our Global Safety Writing Team.

This team handles the preparation of key safety documents such as:

  • Aggregate safety reports

  • Responses to regulatory authority assessments

  • Risk Management Plans (RMPs)

Key Responsibilities:

  • Manage the team mailbox and monitor key team- and project-related activities

  • Assist document authors in preparing deliverables

  • Draft planning documents and data requests

  • Format, compile, and file final safety documents

  • Schedule meetings and support overall team logistics

  • Generate and maintain compliance metrics

  • Ensure quality standards and meet deadlines for assigned tasks

Qualifications:

  • Strong organizational and multitasking skills

  • Excellent attention to detail and ability to meet deadlines

  • Proficient in MS Office tools, especially Word and Excel

  • Good typing skills and fluency in written English

  • Effective oral and written communication

  • Prior experience in pharmacovigilance (preferred)

Ideal Candidate Traits:

  • Proactive and adaptable mindset

  • Strong prioritization and task management

  • Capable of working independently and collaboratively in a remote setup

  • Comfortable with fast-paced and evolving workflows

This role is perfect for individuals seeking to work in the global clinical research space and gain experience in pharmacovigilance writing and documentation support.