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Medical Surveillance Specialist 1

2-6 years
Not Disclosed
10 July 16, 2025
Job Description
Job Type: Full Time Hybrid 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

 

Medical Surveillance Specialist 1 – Bengaluru

Location: Bengaluru, India
Job Type: Full-time
Work Mode: Hybrid
Experience Level: 2 to 6 years
Salary Range: Not specified


Job Summary

IQVIA is hiring a Medical Surveillance Specialist in Bengaluru to provide critical support in clinical data monitoring, narrative writing, and communication with investigator sites. The role involves evaluating clinical lab data from central laboratories and ensuring protocol compliance through proactive surveillance in global clinical trials. This is a hybrid role requiring expertise in clinical lab analysis and healthcare data interpretation.


Key Responsibilities

  • Monitor and evaluate lab data daily from sponsor-designated central laboratories.

  • Analyze laboratory data using eDC platforms and assess deviations from protocol-specific ranges.

  • Compare current and previous lab results to identify clinical significance and escalate issues.

  • Communicate with investigator sites for additional clinical information when necessary.

  • Liaise between Medical Services, central laboratories, and IQVIA project teams.

  • Identify and report potential trends or safety signals in lab data.

  • Support setup and implementation of project-specific surveillance processes.

  • Assist Lead Medical Surveillance Specialists during project initiation.

  • Participate in project team meetings and ensure study objectives are met.


Required Skills & Qualifications

  • Bachelor's degree in Life Sciences, Pharmacy, Biotechnology, Nursing, Physiotherapy, Medical Laboratory Sciences, or similar healthcare disciplines.

  • 2 to 6 years of total experience, with at least 2.5 years in medical surveillance or related roles.

  • Strong knowledge of clinical laboratory data analysis and patient safety monitoring.

  • Experience with data management platforms or eDC systems.

  • Excellent written and verbal communication skills.

  • Proficiency in Microsoft Word and Excel.

  • Strong analytical, organizational, and time management skills.

  • Ability to work collaboratively with cross-functional teams and global clients.


Perks & Benefits

  • Be part of global safety and surveillance initiatives with a leading CRO.

  • Hybrid work flexibility supporting work-life balance.

  • Access to international training programs and continuing education.

  • Collaborative work environment in cutting-edge life sciences research.

  • Exposure to global clinical safety regulations and compliance frameworks.


Company Overview

IQVIA is a global leader in clinical research, real-world data analytics, and healthcare technology. The company partners with top pharmaceutical and life sciences organizations to accelerate innovation, ensure compliance, and improve patient outcomes through smart data-driven solutions.


Work Mode

Hybrid – Based in Bengaluru, with flexibility to collaborate with global teams and support remote operations as needed.


Call to Action

If you’re a healthcare professional passionate about clinical lab monitoring, data integrity, and patient safety, apply today to join IQVIA’s expert medical surveillance team.