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

Safety & Pv Specialist I

Syneos Health
Syneos Health
1-3 years
Not Disclosed
10 Jan. 1, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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: Safety & PV Specialist I
Category: Pharmacovigilance / Drug Safety
Location: Remote, India
Employment Type: Full-Time
Job ID: 25104378


About Syneos Health

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization, dedicated to accelerating the delivery of therapies and improving patient outcomes globally. With a presence in 110 countries and a workforce of over 29,000 employees, we provide innovative solutions across clinical development, medical affairs, and commercial operations.

Our Clinical Development model centers patients and customers in every decision, and we are committed to simplifying processes while fostering a collaborative and inclusive work environment.


Role Overview

We are seeking a Safety & PV Specialist I to join our pharmacovigilance team. In this role, you will be responsible for processing Individual Case Safety Reports (ICSRs), ensuring data accuracy, regulatory compliance, and timely reporting in alignment with ICH GCP, GVP, and global safety regulations. You will support clinical development and post-marketing programs while contributing to the detection of safety signals and risk management initiatives.


Key Responsibilities

  • Receive, triage, and process ICSRs using company PVG systems and tracking tools.

  • Evaluate case data for completeness, accuracy, and reportability according to SOPs and project-specific safety plans.

  • Enter safety data, code adverse events, medical history, concomitant medications, and tests.

  • Compile narrative summaries, identify missing information, and follow up until queries are resolved.

  • Assist in generating expedited safety reports in compliance with regulatory requirements.

  • Maintain safety tracking and perform literature screening for safety signals.

  • Conduct MedDRA coding, maintain drug dictionaries, and validate product records (xEVMPD) including indications coding.

  • Identify and manage duplicate ICSRs and perform quality reviews.

  • Ensure relevant documentation is submitted to Trial Master File (TMF) and Pharmacovigilance System Master File.

  • Maintain compliance with global drug/biologic/device regulations, GCP, ICH guidelines, GVP, SOPs, and project plans.

  • Participate in audits, internal training, and continuous process improvement initiatives.

  • Foster professional relationships with team members, internal stakeholders, and external clients.


Qualifications & Experience

  • Education: Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or equivalent.

  • Experience: Minimum 1–3 years in pharmacovigilance or drug safety, with hands-on exposure to safety database systems.

  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint), email, and shared content management platforms.

  • Strong understanding of clinical trial processes across Phases II–IV and post-marketing safety requirements.


Skills & Competencies

  • Strong knowledge of medical terminology, safety coding, MedDRA, and PV systems.

  • Excellent written and verbal communication skills in English.

  • Ability to work independently and collaboratively in a remote team environment.

  • Highly detail-oriented with strong organizational and multitasking capabilities.

  • Knowledge of safety reporting regulations and guidelines across EU, US, and global markets.

  • Ability to prioritize tasks and meet project deadlines.


Why Join Syneos Health

  • Work with a global leader in clinical development and pharmacovigilance supporting FDA-approved drugs and EMA-authorized products.

  • Gain exposure to international clinical trials, including innovative approaches in safety signal detection and risk management.

  • Be part of a diverse and inclusive culture that encourages professional growth, skill development, and peer recognition.

  • Contribute to meaningful work that improves patient safety worldwide.


Equal Opportunity Employer: Syneos Health is committed to creating a diverse, inclusive, and authentic workplace. We encourage applicants with transferable skills to apply. Reasonable accommodations are available to individuals with disabilities during the recruitment process.