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Safety & Pv Ops Specialist Ii - Technology Support (Argus Console Or Veeva Safety Preferred)

0-2 years
Not Disclosed
10 Oct. 10, 2025
Job Description
Job Type: Full Time Remote 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 Ops Specialist II – Technology Support
(ARGUS Console or Veeva Safety preferred)

Company: Syneos Health
Location: Remote – Chile (CHL)
Job ID: 25101877
Updated: Yesterday


About Syneos Health

Syneos Health® is a fully integrated biopharmaceutical solutions organization that accelerates client success by translating clinical, medical affairs, and commercial insights into actionable outcomes.

  • Our Clinical Development model centers on patients and customers.

  • We aim to simplify processes, enhance collaboration, and accelerate delivery of therapies.

  • Over 29,000 employees in 110 countries work together to transform patient care.

Work Here Matters Everywhere.


Why Join Syneos Health

  • Career development and progression opportunities

  • Supportive and engaged line management

  • Technical and therapeutic area training

  • Peer recognition and total rewards program

  • Commitment to Total Self culture, promoting authenticity and inclusion

  • Inclusive workplace fostering diversity of thought, background, and perspective


Position Summary

The Safety & PV Ops Specialist II – Technology Support ensures regulatory compliance, system accuracy, and data integrity for pharmacovigilance (PV) operations. The role involves supporting safety databases such as ARGUS Console or Veeva Safety, contributing to projects, and maintaining operational excellence.


Key Responsibilities

General Responsibilities

  • Develop and maintain Job Aids and process documentation.

  • Ensure compliance with SOPs, Policies, and SMPs.

  • Maintain up-to-date knowledge of FDA/EU/ICH guidelines for PV reporting.

  • Support annual revenue targets by collaborating with operational teams and Project Managers.

  • Provide metrics and updates as required.

  • Perform other work-related duties as assigned.

Technology Responsibilities

  • Manage and maintain Safety Databases, including:

    • User setup and maintenance

    • Project-specific configurations

    • Routine patches and updates

    • MedDRA and WHO Drug Dictionary updates

    • Performance Qualification (PQ) scripts for updates/changes

    • System maintenance for reporting compliance

  • Assist with other SPVG applications (e.g., SharePoint).

  • Support data migrations, queries, and report generation.

  • Participate in project meetings and provide technical guidance.

  • Ensure compliance with regulatory requirements, company policies, and standards.

  • Maintain expertise in Safety & PV systems through internal meetings and professional development.

  • Support other SPVG initiatives as needed.


Qualifications

Education

  • Bachelor’s degree in Life Sciences, Pharmacy, Nursing, Computer Science, or related technical field.

  • Equivalent combinations of education and experience considered.

Skills & Experience

  • Experience with Safety Database systems (ARGUS Console or Veeva Safety preferred).

  • Knowledge of medical terminology and pharmacovigilance principles.

  • Understanding of ICH guidelines and global safety regulations.

  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Visio, Outlook).

  • Strong communication, presentation, and interpersonal skills.

  • Excellent organizational, documentation, and time management abilities.

  • Attention to detail, accuracy, and ability to meet deadlines.

  • Ability to manage multiple priorities and work independently or in a team.


About Syneos Health’s Global Impact

  • Partnered in 94% of Novel FDA Drug Approvals (past 5 years)

  • Supported 95% of EMA Authorized Products

  • Delivered 200+ clinical studies across 73,000 sites and 675,000+ trial patients


Additional Information

  • Duties and responsibilities may change at the company’s discretion.

  • Equivalent education and experience may be considered.

  • Syneos Health is committed to diversity, equality, and inclusion.

  • Reasonable accommodations provided under ADA to support applicants and employees.


How to Apply


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