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Safet Associate

1-2 years
Not Disclosed
10 June 19, 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 Associate

Job Summary

IQVIA, a global leader in healthcare intelligence and clinical research services, is seeking a Safety Associate for its Kolkata office. This full-time role involves reviewing, processing, and distributing safety data in compliance with global regulatory standards and project-specific guidelines. Ideal for candidates with a scientific background and keen attention to pharmacovigilance practices, this opportunity offers a structured environment to develop expertise in drug safety operations.


Key Responsibilities

  • Review, assess, and process safety data as per regulatory guidelines and SOPs.

  • Perform pharmacovigilance activities such as AE tracking, database entry, narrative writing, coding, and literature review.

  • Meet quality and productivity standards in line with project requirements.

  • Ensure strict adherence to project timelines, deliverables, and processes.

  • Identify and report quality issues to senior team members.

  • Mentor and guide new team members when assigned.

  • Attend project meetings and provide feedback on operational challenges.

  • Maintain 100% compliance with people practices and company policies.

  • Perform other duties as assigned by management.


Required Skills & Qualifications

  • Bachelor’s Degree in scientific/healthcare discipline or allied life sciences (mandatory).

  • 1 to 1.5 years of relevant experience in pharmacovigilance or clinical safety.

  • Good knowledge of medical terminology.

  • Familiarity with safety databases and clinical research regulatory requirements.

  • Proficiency in Microsoft Office and web-based applications.

  • Strong attention to detail, organizational, and time management skills.

  • Good verbal and written communication skills.

  • Ability to multitask, prioritize, and meet deadlines.

  • Flexibility to work in shifts as required.

  • Capability to work both independently and as part of a team.


Perks & Benefits

  • Opportunity to work with a global leader in clinical research and healthcare data analytics.

  • Professional growth and development through cross-functional pharmacovigilance training.

  • Exposure to global clinical safety and regulatory standards.

  • Supportive work environment with mentorship opportunities.

  • Flexibility with shift operations.

  • Occasional travel opportunities, if required.


Company Description

IQVIA is a world-renowned provider of clinical research services, healthcare analytics, and commercial insights, serving the global life sciences industry. The company is dedicated to accelerating innovation and enhancing patient outcomes across diverse therapeutic areas.


Work Mode

On-site (Kolkata, India)


Salary/Compensation

Not explicitly mentioned; compensation will be based on candidate qualifications and experience.


Call to Action

Interested in building a career in drug safety with a global leader? Apply now for the Safety Associate role at IQVIA and contribute to advancing healthcare research worldwide. Last date to apply: June 24, 2025.