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Remote Oracle Argus Safety information

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How much do remote oracle argus safety jobs pay per hour?

As of Jul 21, 2026, the average hourly pay for remote oracle argus safety in the United States is $32.38, according to ZipRecruiter salary data. Most workers in this role earn between $25.48 and $39.18 per hour, depending on experience, location, and employer.

What are some common challenges faced by professionals working in a remote Oracle Argus Safety role?

In a remote Oracle Argus Safety position, one common challenge is ensuring seamless communication and collaboration with global pharmacovigilance teams, especially when handling time-sensitive case processing or regulatory reporting. Additionally, remote professionals must navigate secure access to sensitive data and maintain compliance with strict data privacy protocols. Staying updated with evolving regulatory requirements and software updates is also essential, as is managing workload efficiently when working independently. Strong organizational skills and proactive communication are key to overcoming these challenges and maintaining high-quality safety data management.

What is a Remote Oracle Argus Safety professional?

A Remote Oracle Argus Safety professional is a specialist who manages pharmacovigilance tasks using the Oracle Argus Safety software while working off-site. They are responsible for case processing, adverse event reporting, data entry, and ensuring compliance with regulatory requirements for drug safety. By working remotely, they use secure systems to access and manage sensitive safety data for pharmaceutical companies or clinical research organizations. Their expertise helps ensure that drugs on the market are monitored for safety, protecting patient health worldwide.

What is the difference between Remote Oracle Argus Safety vs Remote Pharmacovigilance Associate?

AspectRemote Oracle Argus SafetyRemote Pharmacovigilance Associate
CertificationsOracle Argus Safety certification, pharmacovigilance trainingPharmacovigilance training, sometimes Oracle Argus Safety knowledge
Work EnvironmentClinical safety departments, CROs, pharmaceutical companiesPharmacovigilance teams, clinical research organizations
Industry UsageUsed for safety data management and adverse event reportingMonitoring, reporting, and managing drug safety data

Remote Oracle Argus Safety professionals focus on managing safety data using Oracle Argus Safety software, often requiring specific certifications. Remote Pharmacovigilance Associates handle adverse event reporting and safety monitoring, sometimes with overlapping skills but generally less specialized in software. Both roles are vital in drug safety and often work in similar environments within the pharmaceutical industry.

What are the key skills and qualifications needed to thrive as a Remote Oracle Argus Safety professional, and why are they important?

To thrive as a Remote Oracle Argus Safety professional, you need expertise in pharmacovigilance processes, strong knowledge of drug safety regulations, and experience with Argus Safety software, often supported by a relevant life sciences degree. Familiarity with database management, case processing, and certifications in Oracle Argus Safety or related pharmacovigilance systems are highly valued. Attention to detail, analytical thinking, and effective remote communication are crucial soft skills for success in this role. These skills ensure accurate case processing, regulatory compliance, and timely collaboration in global, distributed pharmacovigilance teams.
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Remote Oracle Argus Safety jobs near you
Infographic showing various Remote Oracle Argus Safety job openings in the United States as of July 2026, with employment types broken down into 2% Locum Tenens, 87% Full Time, 2% Part Time, 1% Contract, 6% Nights, and 2% Summer. Highlights an 88% Physical, 5% Hybrid, and 7% Remote job distribution, with an average salary of $67,344 per year, or $32.4 per hour.
Associate Director, Safety and Pharmacovigilance

Associate Director, Safety and Pharmacovigilance

Kyverna Therapeutics

Emeryville, CA • On-site, Remote

$170K - $200K/yr

Full-time

Re-posted 13 days ago

Job description

Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients suffering from autoimmune diseases. Guided by our core values, Stay True to Why, Collaborate to Accelerate, Lead with Clarity, Boldly Innovative, and Own the Outcome, we are committed to transforming the future of treatment for autoimmune disease. Join us at the forefront of cell therapy innovation and help redefine what's possible.

Title: Associate Director, Safety and Pharmacovigilance

Reports to: Senior Vice President, Head of Safety

Location: Emeryville, CA (Hybrid) or remote

Summary

The Associate Director of Safety and Pharmacovigilance will be an integral part of the Global Patient Safety and PV team, supporting both PV operations and safety science/risk management activities for assigned investigational and marketed products. The individual will contribute across case/vendor oversight, compliance, signal management, aggregate reporting, and benefit-risk evaluation.

Responsibilities

General

  • Ensure adherence to report timelines and communicate issues to management as appropriate
  • Develop and maintain an expert understanding of the latest safety regulations, technology, and safety profile of the assigned product(s) as well as understanding of the relevant strategic context (e.g., disease indication, safety profile of competitors, mechanism of action)

PV Operations/Quality Assurance

  • Manage and support the relationship with safety vendors to ensure effectiveness, quality and compliance of all outsourced activities in collaboration with Director of PV operations.
  • Lead oversight of quality and key performance indicators (case processing and aggregate reports) and present findings to Head of PV and relevant cross-functional stakeholders.
  • Serve as resource for inspections and audits
  • Ensure operational outputs support high-quality scientific safety assessment

Clinical Safety and Safety Science

  • Lead signal detection and management activities, including literature search, data analyses, preparation of safety data for cross-functional safety team meetings, and drafting presentations and regulatory responses, in collaboration and consultation with the safety physician.
  • Lead the drafting of safety sections of IB, aggregate reports (e.g. PADERs, PSURs, PBRERs, DSURs), and Risk Management Plans etc., in collaboration and consultation of the safety team and the cross-functional teams.
  • Support and contribute to global regulatory submissions (e.g. drafting response to Health Authority requests, authoring and reviewing submission packages, etc.) with the safety team and the cross-functional experts.

The above statements are intended to describe the nature of work performed by those in this job and are not an exhaustive list of all duties. Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job at any time which reflects management's assignment of essential functions.

Qualifications

Education

  • Bachelor's Degree in a scientific, life sciences, or medical field; advanced degree in life science, epidemiology, or (certification/licensure) in Nursing or pharmacology preferred

Experience

  • Minimum 8 years of experience working within Pharmacovigilance, experience with both PV operations and clinical safety/safety science (e.g., signal detection, risk management, regulatory responses) required
  • Experience with neurology or autoimmune diseases preferred
  • Advanced knowledge of safety databases (i.e., Argus), MedDRA coding, signal detection, aggregate reports, and RMPs required
  • Understanding of how AI can be applied in Pharmacovigilance is a plus

Skills

  • Advanced knowledge of Good Pharmacovigilance Practices - both U.S. and European Regulations and Directives, CIOMS/MedWatch
  • Advanced knowledge of Working Group, Code of Federal Regulations, International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH)
  • Excellent ability to analyze and effectively communicate product safety information
  • Demonstrates an attention to detail, results oriented, and good organizational skills
  • Self-motivated with the ability to work both independently and collaboratively within a team environment
  • Ability to adapt quickly to a changing business environment

The national salary range for this position is from $170K to $200K USD annually. This salary range is an estimate of what we reasonably expect to pay for this position, and the actual salary may vary based on various factors, including without limitation individual education, experience, tenure, skills and abilities, as well as internal equity and alignment with market data.  This position is also eligible for bonus, benefits, and participation in Company's stock plan.

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