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Safety & Pv Specialist I (Gurugram-Night Shift)

Syneos Health
3-4 years
INR 8-14 LPA
Gurugram, Haryana, India
10 June 17, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Communication Skills, CPC Certified, CPT, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, HCPCS Level II, ICD-10-CM, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICD-10-PCS, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding

Key Responsibilities

ICSR Processing

  • Receive and track Individual Case Safety Reports (ICSRs).

  • Perform ICSR triage and case assessment.

  • Evaluate case completeness and reportability.

  • Process cases according to SOPs and safety plans.

Safety Database Management

  • Enter safety data into PV databases.

  • Maintain case tracking systems.

  • Ensure data quality and accuracy.

Medical Coding

Perform coding of:

  • Adverse Events

  • Medical History

  • Concomitant Medications

  • Laboratory Tests

  • Drug Products

Using:

  • MedDRA

  • Drug Dictionaries

Narrative Writing

  • Prepare complete medical narratives.

  • Summarize case information accurately.

  • Ensure regulatory compliance of narratives.

Case Follow-Up Activities

  • Identify missing information.

  • Raise and manage follow-up queries.

  • Track resolution of outstanding queries.

Regulatory Reporting

  • Support expedited safety reporting.

  • Assist in regulatory submission activities.

  • Ensure timely reporting as per global regulations.

Literature Review & Screening

  • Conduct literature searches and reviews.

  • Identify reportable safety information.

  • Support pharmacovigilance surveillance activities.

xEVMPD Activities

  • Validation and submission of xEVMPD product records.

  • MedDRA coding of indication terms.

  • Product data maintenance activities.

Duplicate Management

  • Identify duplicate ICSRs.

  • Perform duplicate reconciliation.

  • Maintain case consistency.

SPOR / IDMP Activities

  • Support SPOR data management.

  • Assist with IDMP compliance activities.

Quality Review

  • Perform quality review of ICSRs.

  • Ensure compliance with project requirements.

  • Support continuous quality improvement initiatives.

TMF & Documentation

  • Submit documents to:

    • Trial Master File (TMF)

    • Pharmacovigilance System Master File (PSMF)

  • Maintain inspection-ready documentation.

Audit Support

  • Participate in audits and inspections.

  • Support audit readiness activities.


Required Qualifications

Education

Accepted Degrees

✅ B.Pharm

✅ M.Pharm

✅ BDS

✅ BAMS/BMS (as specified by company)

✅ MBBS

Not Eligible

❌ B.Sc.

❌ M.Sc.


Experience Required

Minimum Experience

2.6+ Years

Mandatory experience in:

  • Pharmacovigilance

  • Drug Safety

  • ICSR Processing

  • Case Processing


Technical Skills Required

Pharmacovigilance Skills

  • ICSR Processing

  • Case Triage

  • Case Assessment

  • Safety Reporting

  • Narrative Writing

  • Follow-Up Management

Coding Skills

  • MedDRA Coding

  • Drug Coding

  • Medical Terminology

Regulatory Knowledge

Strong understanding of:

  • ICH Guidelines

  • GCP

  • GVP

  • FDA Safety Reporting Requirements

  • EMA Safety Regulations

  • Global PV Compliance

Safety Systems

Experience with:

  • Safety Databases (Argus, ARISg, etc.)

  • Tracking Systems

  • Case Management Systems

Specialized Areas

  • xEVMPD

  • SPOR

  • IDMP

  • Duplicate Management


Soft Skills Required

Communication Skills

  • Written communication

  • Verbal communication

  • Cross-functional collaboration

Professional Skills

  • Attention to detail

  • Problem-solving

  • Time management

  • Accuracy-focused approach

  • Teamwork and collaboration


Preferred Candidate Profile

  • Immediate joiners

  • Early joiners

  • Previous CRO experience

  • Experience handling global safety cases

  • Experience with quality review activities

  • Knowledge of European pharmacovigilance requirements