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Argus Safety Jobs (NOW HIRING)

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 ...

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 ...

Verastem

Senior PV Operations Specialist

Boston, MA

Experience with Argus safety databases, EDC systems, and electronic document management systems. * Knowledge of GCPs, GVPs, FDA, EMA, ICH guidelines, and international regulations. * Proficiency in ...

Verastem

Senior PV Operations Specialist

Boston, MA · On-site

$116K - $143K/yr

Experience with Argus safety databases, EDC systems, and electronic document management systems. * Knowledge of GCPs, GVPs, FDA, EMA, ICH guidelines, and international regulations. * Proficiency in ...

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

$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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How much do argus safety jobs pay per hour?

As of Jul 3, 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 June 2026, with employment types broken down into 1% As Needed, 96% Full 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.
Pharmacovigilance Scientist

Pharmacovigilance Scientist

Tonix Pharmaceuticals

Berkeley Heights, NJ

Other

Posted 2 days ago

Job description

Position Overview

Tonix is seeking an experienced Pharmacovigilance Scientist to join our Drug Safety and Pharmacovigilance team. Reporting to the Associate Director, Drug Safety and Pharmacovigilance this role is pivotal in ensuring the safety profiles of our products are effectively monitored and assessed. The PV Scientist will play a key role in cumulative safety data reviews, safety surveillance, and regulatory reporting.

Essential Duties

  • Perform cumulative safety data reviews across trials or programs to assess safety profiles and identify emerging risks or trends
  • Coordinate and document ongoing safety surveillance activities. Activities will include safety data review, signal validations, signal evaluations, literature reviews
  • Lead aggregate report (PSUR/PADER/DSUR) activities, including vendor oversight and project management, database requests, data analysis, report authoring, and quality checks
  • Manage literature review plan for assigned product(s) and provide feedback to vendor on routine literature surveillance activities
  • Coordinate responses for ad hoc safety queries (eg, health authority requests) in collaboration with the cross functional team members, as needed. Perform safety data analyses, draft query responses, and prepare documents for cross functional review and finalization
  • Represent safety at cross functional product meetings
  • For investigational product(s): Support activities relevant to investigational program including (but not limited to):
  • Routine/ad hoc updates to safety content of Investigator Brochure (IB), safety content of protocols, CRFs, ICFs
  • Ongoing data review, including lab, vitals, ECG, and AE data review
  • Review preliminary data and prepare presentations for safety review committees
  • Maintain strong working knowledge of relevant regulations associated with the above activities
  • Contributes to initiatives for process improvement and cross-product process consistency
  • Other tasks as assigned or required

Necessary Skills and Abilities

  • Demonstrated experience in analysis and interpretation of medical and scientific data and excellent verbal and written skills
  • Demonstrated ability to work effectively either independently or collaboratively in a team environment (including Safety, Clinical Development, Medical Affairs, Clinical Operations, and Regulatory), as well as with external colleagues
  • Demonstrated ability to prioritize multiple assignments and proactively identify solutions, as needed
  • Strong organizational, project management and leadership skills: Leads and conducts (independently and/or collaboratively) all aspects of substantive projects such as signaling, authoring of aggregate data reports, and responses to regulatory agency requests.
  • Scientifically sound and clinically accurate approaches to interpret data involving patient safety.
  • Familiarity with pharmacovigilance and drug development, including knowledge of applicable clinical trial safety regulations and post-marketing safety regulations. Includes familiarity with case processing, expedited reporting rules, and safety database concepts
  • Strong knowledge of common data processing software (EXCEL, PowerPoint, Microsoft Word, Business Objects), MedDRA, and Argus Safety System

Education and Experience Requirements

  • Advanced degree in a relevant healthcare or life sciences field (e.g., PharmD, MD, PhD, MPH, or equivalent clinical degree such as RN or NP).
  • Minimum 5 years relevant medical, scientific/clinical, or pharmaceutical experience, including 3 years of experience in drug safety serving in a PV Scientist role

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