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Safety & Pv Submission Specialist Ii

Syneos Health
4+ years
INR 18-14 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

Role Summary

Syneos Health is looking for an experienced Safety & PV Submission Specialist II to manage and coordinate safety reporting and pharmacovigilance submissions for clinical trials and post-marketing programs.

The role involves preparing safety submission plans, ensuring compliance with global regulations, managing expedited and periodic safety reports, maintaining Trial Master File (TMF) documentation, and serving as a key point of contact for regulatory safety submission activities.


Key Responsibilities

Safety Reporting & Submissions

  • Collaborate with Sponsors and project teams on safety reporting activities.

  • Prepare, review, and assemble expedited and periodic safety reports.

  • Develop Safety Reporting Plans for submission-only projects.

  • Maintain tracking systems for safety submissions.

  • Provide regular submission status updates to sponsors and stakeholders.

  • Ensure timely submission of safety reports to regulatory authorities.

Regulatory Compliance

  • Apply global safety reporting regulations and intelligence.

  • Support compliance with:

    • FDA Regulations

    • EMA Regulations

    • India Safety Guidelines

    • ICH GCP

    • GVP Requirements

Project Management

  • Participate in project launch activities.

  • Lead safety submission-related projects.

  • Monitor team workload and project timelines.

  • Support project review meetings.

TMF & Documentation Management

  • Maintain Trial Master File (TMF) documentation.

  • Ensure filing of safety-related documents according to SOPs.

  • Submit documents to:

    • Trial Master File (TMF)

    • Pharmacovigilance System Master File (PSMF)

Metrics & Reporting

  • Track submission cycle times and KPIs.

  • Generate project progress reports.

  • Support quality and performance metrics collection.

Audit Support

  • Participate in internal and external audits.

  • Maintain audit readiness.

  • Support inspection-related activities.

Stakeholder Management

  • Act as the primary contact for safety submission regulatory issues.

  • Collaborate with Sponsors, Ethics Committees, Regulatory Authorities, and internal teams.


Required Qualifications

Education

Bachelor's Degree in:

  • Life Sciences

  • Pharmacy

  • Nursing

  • Related Healthcare Discipline

OR

Equivalent combination of education and relevant experience.


Experience Required

Mandatory Experience

  • Minimum 4+ years of Safety & Pharmacovigilance experience

  • Experience in:

    • Safety Reporting

    • Safety Submissions

    • Pharmacovigilance Operations

Preferred Experience

  • Clinical Research Organization (CRO) experience

  • Regulatory Authority safety submissions

  • Ethics Committee submissions

  • Site safety reporting

  • TMF Filing and Oversight

  • Leading safety submission projects


Technical Skills Required

Pharmacovigilance & Safety

  • Safety Reporting

  • Pharmacovigilance Operations

  • Safety Submission Management

  • Expedited Reporting

  • Periodic Safety Reports

Regulatory Knowledge

Strong knowledge of:

  • ICH GCP

  • GVP Guidelines

  • FDA Regulations

  • EMA Regulations

  • India Regulatory Guidelines

  • Clinical Trial Regulations

Systems Knowledge

  • Safety Databases

  • TMF Systems

  • Document Management Systems

Software Skills

  • Microsoft Word

  • Microsoft Excel

  • Microsoft PowerPoint

  • Microsoft Visio

  • Outlook

  • TeamShare or similar collaboration platforms


Soft Skills Required

  • Strong communication skills

  • Presentation skills

  • Stakeholder management

  • Project coordination

  • Attention to detail

  • Decision-making ability

  • Time management

  • Ability to prioritize multiple projects

  • Independent and team-based working capability


Travel Requirement

  • Up to 5% travel