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Remote Oracle Argus Safety Jobs (NOW HIRING)

A.C. Coy

Oracle Developer (Remote)

Columbus, OH · Remote

$54.50 - $67.75/hr

... seeking an Oracle Developer for our direct US Government client. * This will be a 100% remote ... safety. * Identify problems uncovered by testing or customer feedback and correct problems.

A.C. Coy

Oracle Developer (Remote)

Columbus, OH · On-site +1

$54.50 - $67.75/hr

... seeking an Oracle Developer for our direct US Government client. * This will be a 100% remote ... safety. * Identify problems uncovered by testing or customer feedback and correct problems.

A.C. Coy

Oracle Developer (Remote)

Columbus, OH · Remote

$54.50 - $67.75/hr

... seeking an Oracle Developer for our direct US Government client. * This will be a 100% remote ... safety. * Identify problems uncovered by testing or customer feedback and correct problems.

ICU Medical

Applications Programmer/EDI Oracle

... medication safety software providing full IV-EHR interoperability with the highest customer ... This role is based remotely; the incumbent may be remote in any state other than Colorado;

Apex IT

Oracle Cloud HCM Solution Architect

$64.50 - $85/hr

Work is remote or on-site at the customer location. Travel is required. The percentage of travel to ... Health & Safety § Oracle Cloud Talent Management • Workforce Compensation • Learning • ...

Spectra force

Medical Safety Physician

Lincolnton, NC · On-site +1

Company Description Medical Safety Physician 6-month assignment 100% Remote What are the three most important qualifications: Argus experience, self starter, experience in pharmacovigilance and ...

SPECTRAFORCE

Medical Safety Physician

Lincolnton, NC · Remote

Medical Safety Physician 6-month assignment 100% Remote What are the three most important qualifications: Argus experience, self starter, experience in pharmacovigilance and infection disease ...

Oracle

Senior Data Center Construction Manager

Abilene, TX · On-site +1

$50 - $67.75/hr

... safety and quality expectations, and supporting turnover readiness for commissioning and startup ... miles from the Oracle Cloud Infrastructure Abilene AI Data Center. It does not offer remote ...

Oracle

Senior Data Center Construction Manager

Abilene, TX · On-site +1

$50 - $67.75/hr

... safety and quality expectations, and supporting turnover readiness for commissioning and startup ... miles from the Oracle Cloud Infrastructure Abilene AI Data Center. It does not offer remote ...

Oracle

Senior Data Center Construction Manager

Abilene, TX · On-site +1

$117K/yr

... safety and quality expectations, and supporting turnover readiness for commissioning and startup ... miles from the Oracle Cloud Infrastructure Abilene AI Data Center. It does not offer remote ...

Oracle

Senior Data Center Construction Manager

Abilene, TX · On-site +1

$117K/yr

... safety and quality expectations, and supporting turnover readiness for commissioning and startup ... miles from the Oracle Cloud Infrastructure Abilene AI Data Center. It does not offer remote ...

Oracle

Senior Data Center Construction Manager

Abilene, TX · On-site +1

$50 - $67.75/hr

... safety and quality expectations, and supporting turnover readiness for commissioning and startup ... miles from the Oracle Cloud Infrastructure Abilene AI Data Center. It does not offer remote ...

Oracle

Senior Data Center Construction Manager

Abilene, TX · On-site +1

$50 - $67.75/hr

... safety and quality expectations, and supporting turnover readiness for commissioning and startup ... miles from the Oracle Cloud Infrastructure Abilene AI Data Center. It does not offer remote ...

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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.
Director, Drug Safety and Pharmacovigilance

Director, Drug Safety and Pharmacovigilance

BridgeBio Pharma

Remote

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 4 days ago

Job description

Mavericks Wanted
When was the last time you achieved the impossible? If that thought feels overwhelming, you might want to pause here, but if it sparks excitement...read on
In 2015, we pioneered a "moneyball for biotech" approach, pooling projects and promising early-stage research from academia together under one financial umbrella to reduce risk and unleash innovation. This model allows science and small teams of experts to lead the way. We build bridges to groundbreaking advancements in rare disease, and develop life-changing medicines for patients with unmet needs as fast as humanly possible.
Together we define white space, push boundaries, and empower people to solve problems. If you're someone who defies convention, join us and work alongside some of the most respected minds in the industry. Together, we'll ask "why not?" and help reengineer the future of biopharma. At BridgeBio, we value curiosity and experimentation-including the ethical & thoughtful use of AI to improve clarity, speed, and quality of work.
What You'll Do
  • Serve as the business-side system owner and subject matter expert for the Veeva Safety platform, ensuring the system is compliantly configured, validated, and operationally effective in support of Eidos' global pharmacovigilance program.

Responsibilities
  • Configure and administer the Veeva Safety platform (Vault Safety Suite: Safety, SafetyDocs, Signal, Workbench), including user administration, workflow routing, coding configurations (MedDRA, WHO Drug), and business rules
  • Author and execute validation documentation in accordance with 21 CFR Part 11, GxP, and GAMP 5 principles, including User Requirements Specifications (URS), IQ/OQ/PQ protocols, UAT scripts, and traceability matrices
  • Lead User Acceptance Testing (UAT) cycles for new releases, configuration changes, and system enhancements; maintain change control governance
  • Configure and run safety reports and operational dashboards within Veeva Safety; ensure all outputs are validated and fit for regulatory submission or internal review
  • Apply expert knowledge of the end-to-end adverse event lifecycle to inform system design and support case processing operations
  • Ensure system configuration supports compliance with global ICSR reporting timelines (7-day, 15-day) and periodic reporting frameworks (IND, NDA/PADER, PBRER/PSUR, DSUR)
  • Maintain current knowledge of worldwide pharmacovigilance regulations including ICH E2B(R2/R3), FDA, EMA, PMDA, and MHRA requirements; update system configurations accordingly
  • Oversee E2B(R3) gateway configurations for regulatory submissions to EudraVigilance, FDA ESG, and trading partners
  • Support PSMF maintenance activities related to PV system descriptions and IT infrastructure documentation
  • Develop and maintain system SOPs, work instructions, and user training materials; deliver training to system users
  • Lead inspection readiness activities related to the Veeva Safety system; support regulatory audits and agency inspections
  • Partner with IT, Quality, and Regulatory Affairs on system upgrades, integrations, and vendor governance

Where You'll Work
This a U.S-based remote role that will require quarterly, or as needed visits to our San Francisco Office. Travel for unannounced Regulatory Authority Inspections is required.
Who You Are
  • Bachelor's degree in life sciences, pharmacy, nursing, health informatics, or a related field required; advanced degree preferred
  • Minimum 8-10 years of experience in pharmacovigilance or drug safety operations within a pharmaceutical, biotechnology, or CRO environment
  • Demonstrated history of self-direction and accountability
  • Demonstrated Regulatory Agency Inspection history
  • Experience in both clinical trial and post-marketing safety required
  • Direct participation in agency inspections including FDA, EMA, Health Canada and others
  • Management of change management, compliance deviations, and CAPAs
  • Minimum 3-5 years of direct hands-on experience as a business administrator or power user on Veeva Safety (Vault Safety) or comparable safety database (Oracle Argus, ARISg)
  • Demonstrated experience authoring and executing GxP validation documentation (URS, IQ/OQ/PQ, UAT) in a regulated environment
  • Deep knowledge of ICH E2B(R2/R3), MedDRA, WHO Drug coding, and global ICSR reporting requirements
  • Experience with aggregate reporting frameworks: IND, NDA/PADER, PBRER/PSUR, DSUR, and CTPR
  • Experience with Veeva Safety migration projects (e.g., Argus-to-Veeva) a plus
  • Familiarity with AI/automation capabilities for AE processing and MedDRA coding within the Veeva ecosystem preferred
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) required
  • Must be able and willing to travel

At BridgeBio, we strive to provide a market-competitive total rewards package, including base pay, an annual performance bonus, company equity, and generous health benefits. Below is the anticipated salary range for candidates for this role who will work in California. The final salary offered to a successful candidate will depend on several factors that may include but are not limited to the type and length of experience within the job, type, and length of experience within the industry, educational background, location of residence and performance during the interview process. BridgeBio is a multi-state employer, and this salary range may not reflect positions based in other states.
Salary
$222,300-$255,000 USD
As a global company, our comprehensive benefits may vary based on location. We have high expectations for our team members. We make sure those working hard for patients are rewarded and cared for in return.
For Full-Time U.S Based Roles:
Financial & Rewards
  • Market-leading compensation
  • 401(k) with employer match
  • Employee Stock Purchase Program (ESPP)
  • Pre-tax commuter benefits (transit and parking)
  • Referral bonus for hired candidates
  • Subsidized lunch and parking on in-office days

Health & Well-Being
  • 100% employer-paid medical, dental, and vision premiums for you and your dependents
  • Health Savings Account (HSA) with annual employer contributions, plus Flexible Spending Accounts (FSA)
  • Fertility & family-forming benefits
  • Expanded mental health support (therapy and coaching resources)
  • Hybrid work model with flexibility
  • Flexible, "take-what-you-need" paid time off and company-paid holidays
  • Comprehensive paid medical and parental leave to care for yourself and your family

Skill Development & Career Paths:
  • People are part of our growth and success story - from discovery to active drug trials and FDA pipelines, there are endless opportunities for skill development and internal mobility
  • We provide career pathing through regular feedback, continuous education and professional development programs via LinkedIn Learning, LifeLabs, & BetterUp Coaching
  • We celebrate strong performance with financial rewards, peer-to-peer recognition, and growth opportunities

Apply