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Argus Safety Jobs (NOW HIRING)

Global Pharmatek

Drug Safety Assistant

Piscataway, NJ · On-site

Enter applicable information into the global safety database for initial or follow up cases ... Accept E2B cases received through the Argus Electronic Submissions Module (ESM) from European ...

Global Pharmatek

NJ · On-site

Enter applicable information into the global safety database for initial or follow up cases ... Accept E2B cases received through the Argus Electronic Submissions Module (ESM) from European ...

Talent Groups

Drug Safety Specialist

Waltham, MA · On-site

Experience with Argus, ARISg, or similar safety databases , regulatory safety reporting, and oncology case processing is highly preferred. Required Skills & Qualifications: * Clinical degree (RN, BSN ...

Ionis

Director, PV Systems

Carlsbad, CA · On-site +1

This role serves as the primary bridge between PV business operations and the external vendors responsible for maintaining and implementing Ionis's PV technology stack - including Argus Safety ...

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How much do argus safety jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for argus safety in the United States is $25.60, according to ZipRecruiter salary data. Most workers in this role earn between $22.36 and $28.61 per hour, depending on experience, location, and employer.

What is an Argus Safety?

An Argus Safety job typically involves managing drug safety and pharmacovigilance data using Oracle Argus Safety, a widely used software for adverse event reporting. Professionals in this role handle case processing, report adverse events to regulatory authorities, and ensure compliance with global drug safety regulations. They may work in pharmaceutical companies, contract research organizations (CROs), or regulatory agencies. Skills in medical coding, database management, and regulatory reporting are important for success in this field.

What are the key skills and qualifications needed to thrive in the Argus Safety position, and why are they important?

To succeed in an Argus Safety role, you need a strong background in pharmacovigilance, understanding of drug safety regulations, and typically a degree in pharmacy, life sciences, or a related field. Familiarity with Argus Safety database software and knowledge of regulatory reporting systems such as EudraVigilance or FDA MedWatch are crucial. Attention to detail, analytical thinking, and effective communication skills help professionals excel in analyzing safety data and preparing reports. These competencies ensure accurate adverse event processing and regulatory compliance, which are vital for patient safety and organizational success.

What are the typical daily tasks and responsibilities for someone working in an Argus Safety role?

In an Argus Safety role, your daily tasks typically include processing and entering adverse event reports, performing case triage and data validation, and coding medical terms according to regulatory standards. You’ll also review data for accuracy, prepare regulatory submissions, and generate safety reports within the Argus Safety database. Collaboration with pharmacovigilance scientists, clinical teams, and regulatory authorities is common, requiring strong teamwork and communication. Staying organized and maintaining data integrity are essential as you ensure both patient safety and compliance with global regulations.

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Argus Safety jobs near you
Infographic showing various Argus Safety job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 17% Part Time, 2% Contract, and 1% Nights. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $53,254 per year, or $25.6 per hour.

CSV Validation Consultant

Compsciprep LLC

Chicago, IL • On-site

Other

Posted 4 days ago

Job description

Hi,                                      

 
Greetings from CompSciPrep!!!
 
We have an immediate opening for a position with one of our prestigious clients that may interest you.
 
Below is the job description for your reference. Please go through it and let me know your thoughts so that we can move forward.
 
Job Description:
 
Role: Computer System Validation (CSV) / Validation Consultant – Life Sciences
Location: Multiple Location 
 
Summary:
We are looking for an experienced Computer System Validation (CSV) Consultant with strong experience in Life Sciences/Pharmaceutical domain. The ideal candidate should have hands-on expertise in validating GxP regulated systems, ensuring regulatory compliance, and supporting clinical and quality applications.
 
Must Have Skills
  • 8+ years of experience in Computer System Validation (CSV)
  • Strong understanding of GxP, 21 CFR Part 11, GAMP 5, FDA regulations
  • Experience in IT Compliance and validation lifecycle
  • Validation of IT Systems and regulated applications
  • Hands-on experience with Veeva Quality Docs
  • Experience with JIRA and HP ALM
  • Validation of Safety Systems
  • Experience with Argus Safety
  • Experience with Veeva Vault
  • Experience working on Clinical Trial Systems
  • Knowledge of CTMS (Clinical Trial Management System)
  • Preparation and review of validation documents (URS, IQ, OQ, PQ, RTM, Validation Plan, Validation Summary Report)
  • Strong communication and stakeholder management skills
Preferred Skills
  • ISO 13485 / Quality Management exposure
  • Clinical, Quality, and Pharmacovigilance system validation
  • Experience working with global pharmaceutical clients
  • Knowledge of SDLC and Agile methodology
Responsibilities
  • Execute end-to-end Computer System Validation activities.
  • Prepare and review validation documentation.
  • Ensure systems comply with GxP and regulatory requirements.
  • Coordinate with business, QA, IT, and vendors during validation.
  • Support audits and compliance activities.
  • Validate clinical, quality, and safety applications.
 
 

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