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Safety & Pv Specialist I

Syneos Health
Syneos Health
0-2 years
Not Disclosed
10 Dec. 31, 2025
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 & Pharmacovigilance Specialist I
Location: Remote – India
Job ID: 25104378
Experience Required: 0–2 years in Pharmacovigilance or Drug Safety

Company Overview:
Syneos Health® is a global, fully integrated biopharmaceutical solutions organization dedicated to accelerating customer success. By translating clinical, medical affairs, and commercial insights into actionable outcomes, we address modern healthcare challenges while keeping patients at the center of everything we do. With 29,000 employees across 110 countries, Syneos Health drives innovation to deliver therapies efficiently and safely.

Why Join Syneos Health:

  • Structured career development, technical training, and peer recognition programs.

  • Inclusive Total Self culture fostering diversity, equity, and belonging.

  • Opportunities to work across functional service provider partnerships and full-service environments.

  • Active participation in shaping global pharmacovigilance practices and patient safety initiatives.

Job Summary:
The Safety & PV Specialist I is responsible for executing pharmacovigilance activities, ensuring compliance with global regulatory requirements, and supporting clinical safety operations. This role involves processing Individual Case Safety Reports (ICSRs), performing medical coding, assisting with narrative writing, and supporting safety reporting activities under supervision. The specialist contributes to maintaining data integrity, quality, and regulatory compliance throughout the drug lifecycle.

Key Responsibilities:

  • Enter, triage, and track ICSRs in pharmacovigilance databases following SOPs and safety plans.

  • Perform data evaluation for completeness, accuracy, and regulatory reportability.

  • Code adverse events, medical history, concomitant medications, and lab tests using MedDRA.

  • Draft and review narrative summaries for ICSRs.

  • Identify data gaps, follow up on queries, and ensure timely resolution.

  • Assist in expedited report generation in line with regulatory timelines.

  • Conduct literature screening, safety reviews, and product coding maintenance.

  • Validate and submit xEVMPD product records, including indication coding.

  • Identify and manage duplicate ICSRs.

  • Maintain quality standards through ICSR reviews, TMF submissions, and compliance with GCP, ICH, and GVP guidelines.

  • Support audits, regulatory intelligence application, and process improvement initiatives.

Qualifications:

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

  • Knowledge of safety database systems and medical terminology.

  • Understanding of clinical trial phases II–IV, post-marketing safety requirements, and global PV regulations (GVP, ICH, GCP).

  • Proficiency in Microsoft Office (Word, Excel, PowerPoint), Visio, Outlook, Teams, and other digital collaboration tools.

  • Strong communication, interpersonal, and organizational skills.

  • Detail-oriented, capable of managing multiple tasks with high accuracy and adherence to deadlines.

Career Growth & Impact:
This role provides exposure to pharmacovigilance operations, case processing, safety signal detection, and risk management. As an individual contributor, you will collaborate with cross-functional teams, gaining expertise in regulatory compliance and clinical safety processes. This position is ideal for professionals starting their career in drug safety or PV, aiming to advance into senior roles.

How to Apply:
Interested candidates can apply directly through The Pharma Daily Job Portal or join our Talent Network to stay connected with future opportunities.

About Syneos Health:
Over the last five years, Syneos Health has supported 94% of novel FDA-approved drugs, 95% of EMA-authorized products, and over 200 clinical studies across 73,000 sites and 675,000+ trial patients globally. Join a team where your work in pharmacovigilance and patient safety matters everywhere.

Disclaimer:
The responsibilities and qualifications listed are not exhaustive. Equivalent education or experience may be considered. The company may assign additional tasks as required and complies with applicable local employment and disability laws.