Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Senior Safety & Pv Submission Specialist (Gurugram/Hyderabad)

Syneos Health
Syneos Health
4-6 years
upto 9 LPA
Hyderabad
8 April 23, 2026
Job Description
Job Type: Full Time Education: B.Pharm, M.Pharm, Pharm D., BSc., MSc. 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

Senior Safety & Pharmacovigilance Submission Specialist

Location: Gurugram / Hyderabad, India (Hybrid)
Company: Syneos Health
Job ID: 25106996
Experience Required: Minimum 6 years (Not suitable for freshers)


About the Company

Syneos Health is a leading global biopharmaceutical solutions organization that supports end-to-end drug development and commercialization. With a strong global footprint and expertise across clinical research and pharmacovigilance, the organization partners with sponsors to deliver high-quality, compliant, and efficient healthcare solutions.


Job Overview

The Senior Safety & Pharmacovigilance Submission Specialist is responsible for managing and overseeing regulatory safety submissions across clinical trials and post-marketing programs. This role requires deep expertise in pharmacovigilance regulations, safety reporting timelines, and submission processes to global regulatory authorities including FDA, EMA, and Indian health authorities.


Key Responsibilities

  • Collaborate with sponsors and internal project teams for the design, preparation, and submission of expedited and periodic safety reports

  • Develop and maintain Safety Reporting Plans for assigned projects

  • Track and manage end-to-end safety submission activities, ensuring compliance with global regulatory timelines

  • Provide regular submission status updates to sponsors and stakeholders

  • Act as a subject matter expert for safety submission-related regulatory queries

  • Apply global pharmacovigilance regulatory intelligence to all submission activities

  • Ensure accurate filing of safety documents in Trial Master File (TMF) and Pharmacovigilance System Master File (PSMF)

  • Support project teams in resolving safety reporting issues and audit readiness

  • Participate in internal project review meetings and audits

  • Monitor KPIs, cycle times, and submission performance metrics

  • Coordinate workload distribution and support team-level deliverables


Required Qualifications

  • Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or related field

  • Minimum 6 years of experience in Pharmacovigilance and Safety Submissions

  • Proven experience in regulatory safety submissions to authorities such as FDA, EMA, and CDSCO

  • Strong understanding of ICH-GCP, GVP guidelines, and global safety reporting requirements

  • Hands-on experience with safety databases and medical terminology

  • Experience in TMF management and oversight

  • Proficiency in Microsoft Office tools and clinical systems

  • Strong communication, organizational, and stakeholder management skills

  • Ability to work independently and manage multiple projects simultaneously


Preferred Skills

  • Experience working in a CRO environment

  • Exposure to Phase II–IV clinical trials and post-marketing safety reporting

  • Leadership experience in managing safety submission projects


Why This Role Matters

This position plays a critical role in ensuring patient safety and regulatory compliance across global clinical trials and post-marketing surveillance. You will contribute directly to the safe and timely delivery of life-saving therapies to patients worldwide.


Important Note for Applicants

This is a senior-level pharmacovigilance role requiring hands-on experience in safety submissions and regulatory compliance. Freshers or entry-level candidates are advised to apply for roles such as Drug Safety Associate or PV Case Processing Associate to build foundational experience.


How to Apply

Apply through the official careers page of the company or explore verified global pharmacovigilance job opportunities on ThePharmaDaily.com