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41185 - Safety Associate Trainee

0-2 years
₹3.6 – 5.0 LPA
10 Aug. 21, 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 Trainee
Locations: Kolkata, India | Kochi, India
Company: IQVIA
Job Type: Full-Time
Application Deadline: August 23, 2025
Job ID: R1492205

About the Company:
IQVIA is a leading global provider of advanced analytics, clinical research services, and technology solutions for the life sciences industry. We create intelligent connections across healthcare to accelerate innovation and improve patient outcomes worldwide.

Role Overview:
As a Safety Associate Trainee, you will gain hands-on experience in pharmacovigilance operations, supporting the processing of safety data, adverse events, and regulatory documentation. This role is ideal for recent graduates in life sciences or healthcare fields seeking to build a career in drug safety.

Key Responsibilities:

  • Complete all required trainings on time and with high proficiency.

  • Process safety data according to regulations, SOPs, and project-specific requirements.

  • Perform pharmacovigilance activities, including:

    • Collection and tracking of Adverse Events (AEs) and endpoint information.

    • Determining status of events (initial/update).

    • Database entry, AE/product coding, and narrative writing.

    • Literature review and related safety activities.

  • Ensure productivity and quality targets are met consistently.

  • Identify quality issues and escalate to senior team members/mentors.

  • Participate in project team meetings and share operational feedback.

  • Ensure full compliance with people practices and organizational policies.

  • Perform additional responsibilities as assigned by managers.

Qualifications:

  • Bachelor’s degree in a scientific/healthcare discipline (Life Sciences, Pharmacy, Nursing, etc.) required.

  • Strong knowledge of medical terminology.

  • Excellent verbal and written communication skills.

  • Ability to work effectively as part of a team.

  • Good knowledge of Microsoft Office and web-based applications.

  • High attention to detail, accuracy, and time management.

  • Self-motivated, adaptable, and willing to learn new skills.

  • Flexibility to work in shifts and occasional travel if required.

Work Environment:

  • Extensive keyboard usage (data entry).

  • Regular sitting for extended periods.

  • Frequent communication via phone and virtual tools.

Why Join IQVIA?

  • Exposure to end-to-end pharmacovigilance processes.

  • Learning opportunities under senior safety professionals.

  • Strong foundation for career growth in clinical research and drug safety.

  • Be part of a global leader in healthcare intelligence and innovation.

Estimated Salary: ₹3.6 – 5.0 LPA (based on trainee pharmacovigilance industry standards in India).