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Argus Safety Jobs (NOW HIRING)

Global Pharmatek

NJ

Argus experience. Additional Information All your information will be kept confidential according to EEO guidelines.

Viatris

Safety Submission Associate

Morgantown, WV · On-site

$37K - $80K/yr

Oracle Argus) upon receipt acknowledgment and prepares final submission documentation for case ... Assists Lead Safety Submission Specialist in the generation of US PADERs. * Assembles and bookmarks ...

Viatris

Safety Submission Associate

Morgantown, WV · On-site

$37K - $80K/yr

Oracle Argus) upon receipt acknowledgment and prepares final submission documentation for case ... Assists Lead Safety Submission Specialist in the generation of US PADERs. * Assembles and bookmarks ...

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Argus Safety information

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How much do argus safety jobs pay per hour?

As of Jul 24, 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 job?

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 July 2026, with employment types broken down into 5% Locum Tenens, 4% Full Time, 89% Nights, and 2% Summer. Highlights an 88% Physical, 5% Hybrid, and 7% Remote job distribution, with an average salary of $53,254 per year, or $25.6 per hour.
Drug Safety Data Management Specialist

Drug Safety Data Management Specialist

Global Pharmatek

NJ

Contractor

Posted 20 days ago

Job description

Company Description

We are proud to be part of the most precious thing on Earth: human life. Applying the technological expertise to the medical knowledge to derive near infallible results comes naturally to Global Pharma Tek, LLC. Global Pharma Tek is a fast-growing premier global pharmaceutical company that provides end-to-end services in pharmaceutical industry round the globe. Global Pharma Tek offers services like Drug Discovery, Clinical Trials, Drug Delivery, Regulatory and Intellectual Property Rights, Marketing and Strategic Human Resourcing. Global Pharma Tek is specialized in providing highly technical pharmaceutical and healthcare solutions and services in a cost effective way around the globe.

We are enterprise-class clinical software and clinical functional services provider, offers unique blend of both clinical trial domain and core IT expertise with thorough understanding of healthcare and pharma industry and regulatory standards. Global Pharma Tek, clinical functional services practice (FSP) enable pharmaceutical and life sciences industry customers realize their vision of safe, effective, and FDA approved delivery of drug at the lowest cost and at the fastest time to market. 

With core technology focus in the areas of statistical programming, business intelligence & data warehousing, enterprise application integration and enterprise architecture development, enterprise resource planning and custom applications development, along with clinical domain expertise, Global Pharma Tek offers a full range of specialized functional clinical & IT in-sourcing, IT projects development, clinical functional & IT projects outsourcing, software enabled services.

Job Description

Job Description:

  • Enter applicable information into the global safety database for initial or follow up cases received via paper, fax or email.
  • Book-in, quality check and initially assess cases from suppliers sending cases to DSS via paper, email or fax.
  • Accept E2B cases received through the Argus Electronic Submissions Module (ESM) from European Health Authorities on behalf of Pfizer Country Offices that are not online with Argus and other submitters as necessary.
  • Monitor electronic mailboxes and Argus ESM to ensure timely acceptance of Adverse Event (AE) Reports Perform data entry into databases, as needed.
  • Ensure proper coding of events and drugs for cases to ensure correct forwarding to the relevant Therapeutic Area Teams and Licensing Group.
  • Upload AE reports to the Drop in Data Entry II application on behalf of country offices cannot on their own.
Qualifications

BA degree required with 1-3 years of Safety/ Pharmacovigilance Data experience. Argus experience.

Additional Information
All your information will be kept confidential according to EEO guidelines.
Global Pharmatek logo

About Global Pharmatek

Sourced by ZipRecruiter

Global Pharmatek is a leading Contract Research Organization (CRO) and integrated drug discovery solutions provider in the pharmaceutical industry. The company is located in Edison, New Jersey, USA. Their comprehensive range of services includes Drug Discovery, Clinical Trials, Regulatory Affairs, and Biometrics, designed with the goal of swiftly translating scientific innovation into a novel product. Founded with an unwavering commitment to enhance health and well-being worldwide, this leading-edge company lays emphasis on the highest quality standards, efficient delivery, and transparency.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

2011

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