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Medical Surveillance Specialist 1

Iqvia
IQVIA
2-6 years
preferred by company
10 Jan. 13, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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: Medical Surveillance Specialist I

Location: Kochi, Kerala, India
Work Mode: Full-Time | Hybrid
Experience Required: 2–6 Years (Minimum 2.5 Years in Medical Surveillance)
Job ID: R1478911

Job Overview

We are seeking a Medical Surveillance Specialist I to support global clinical research programs through comprehensive medical surveillance activities. This role focuses on continuous monitoring and evaluation of clinical laboratory data, preparation of medical narratives, and effective coordination with investigator sites and cross-functional project teams. The position is ideal for life sciences and healthcare professionals with hands-on experience in medical surveillance and clinical data interpretation.

Key Responsibilities

  • Perform daily monitoring and evaluation of clinical laboratory results received from sponsor-designated central laboratories.

  • Analyze laboratory data at defined intervals using EDC and clinical data management platforms.

  • Conduct preliminary reviews of laboratory results against protocol-specific reference ranges, identifying clinically relevant abnormalities or trends.

  • Compare current laboratory values with historical data to assess clinically significant increases or decreases.

  • Communicate with investigator sites to obtain additional clinical information and ensure timely dissemination of findings to the project team.

  • Act as a key liaison between the Medical Services Department, sponsor-designated laboratories, and project teams.

  • Identify potential safety signals or laboratory trends and escalate concerns to Medical Advisors as appropriate.

  • Collaborate with central laboratory teams to support accurate monitoring, reporting, and documentation of subject laboratory results.

  • Assist the Lead Medical Surveillance Specialist with study setup and ongoing project activities.

  • Participate in project team meetings and contribute to discussions impacting study objectives.

  • Maintain current knowledge of clinical laboratory practices through continuous education and medical seminars.

  • Perform additional duties related to medical surveillance as assigned.

Qualifications & Experience

  • Bachelor’s degree in Life Sciences or Allied Health Sciences, including:

    • Pharmacy, Biochemistry, Microbiology, Biotechnology

    • Nursing, Medical Laboratory Sciences, Physiotherapy

    • Medical disciplines (Allopathy, Homeopathy, Ayurveda) or Dentistry

  • 2–6 years of total relevant experience, with at least 2.5 years of mandatory experience in medical surveillance.

  • Equivalent combinations of education, training, and experience may be considered.

  • Strong ability to interpret, analyze, and integrate clinical and laboratory data from multiple sources.

  • Excellent written and verbal communication skills with the ability to convey complex medical information clearly.

  • Proficiency in data management systems, documentation tools, and clinical databases.

  • High attention to detail with strong analytical and organizational capabilities.

  • Proven ability to build and maintain effective working relationships with internal teams, investigators, and clients.

Why This Role Matters

  • Contribute directly to patient safety and data quality in global clinical trials.

  • Gain exposure to international clinical research projects and regulatory environments.

  • Work in a hybrid model that supports flexibility and professional growth.

  • Build a long-term career in medical surveillance, clinical safety, and clinical research operations.

About IQVIA

IQVIA is a global leader in clinical research services, healthcare intelligence, and commercial insights for the life sciences and healthcare industries. IQVIA enables faster development and commercialization of innovative medical treatments, improving patient outcomes and population health worldwide.

Apply Now

Qualified candidates with medical surveillance experience and a passion for clinical research are encouraged to apply through thepharmadaily.com.


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