Argus Database Programmer Analyst
Location: Remote, India
Job ID: R-01323511
Job Type: Full-time
Department: Clinical Research
Shift: Second Shift (Afternoons)
Estimated Salary: ₹11 – ₹17 LPA (based on current CRO and PV tech standards in India)
About the Role:
Thermo Fisher Scientific is hiring an experienced Argus Database Programmer Analyst to support day-to-day administration and configuration of the Oracle Argus Safety Database. This fully remote role will operate on East Coast U.S. hours, making it ideal for professionals comfortable with second shift timings. You’ll play a critical role in pharmacovigilance technology services, supporting drug safety reporting and compliance across global clinical research operations.
Key Responsibilities:
Serve as the subject matter expert (SME) for Oracle Argus PV safety database
Collaborate with pharmacovigilance (PV) users to understand technical and business requirements
Configure and manage Oracle Argus system, tenants, distribution rules, and change controls
Generate custom and ad-hoc safety reports using built-in tools, SQL, or OBIEE
Lead data migration and validation projects, and develop technical documents (Design Specs, Plans, Summary Reports)
Resolve end-user queries and support Argus dictionary upgrades and enhancements
Liaise with vendors for system upgrades, ongoing maintenance, and troubleshooting
Assist in SOP development and support audits (internal/external) for the safety database
Provide programming support for safety data review and generate high-quality deliverables
Mentor junior staff and lead database improvement initiatives
Ensure compliance with industry standards, SOPs, and applicable regulations
Required Qualifications:
Bachelor’s degree or equivalent in life sciences, computer science, or a related discipline
Minimum 5 years’ experience in pharmacovigilance safety systems administration, particularly with Oracle Argus
Previous case processing experience is desirable
Proven record in Argus J administration and safety data migrations
Strong SQL programming and data management experience
Experience working with relational database structures and transformation rules
Familiarity with pharmacovigilance regulatory requirements and GxP systems
Excellent problem-solving, analytical, and communication skills
Ability to handle multiple tasks independently in a time-sensitive, regulated environment
Strong team collaboration skills and ability to lead project initiatives
Why Join Thermo Fisher Scientific?
Work in a mission-driven global organization committed to health, safety, and innovation
Competitive salary with comprehensive benefits and professional development programs
A truly inclusive, collaborative, and flexible remote work culture
Be part of a leading CRO team supporting the PPD® clinical research portfolio
Grow your career by contributing to groundbreaking clinical and safety innovations
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