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Safety Database Specialist

1-2 years
Not Disclosed
10 Oct. 30, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Safety Database Specialist

📍 Location: Navi Mumbai, India
🏢 Department: Clinical Safety
📄 Job ID: 11432


Job Summary

Medpace is seeking a skilled and detail-oriented Safety Database Specialist to join our Clinical Safety team. This role plays a critical part in maintaining and supporting our global safety systems. If you have a strong technical background, attention to detail, and a desire to make an impact in clinical research, this opportunity is for you.


Key Responsibilities

  • Configure and maintain safety databases (Argus and Argus J) including product, study, and license setups.

  • Create and generate reports using Oracle Business Intelligence (OBIEE) tools.

  • Troubleshoot and resolve safety database-related issues.

  • Prepare and execute User Acceptance Testing (UAT) for safety system updates or changes.

  • Assist in training new users on the Argus database.

  • Generate safety data outputs to support periodic safety reports (DSUR, PSUR, PBRER).

  • Contribute to the development of SOPs, Work Instructions, and user manuals for system support.

  • Provide support during inspections and audits related to safety systems.


Qualifications

Minimum Requirements:

  • Bachelor’s degree in a scientific discipline or Business Informatics, or a related field.

  • 1–2 years of directly related experience.

Preferred Qualifications:

  • Experience in a CRO, biotech, or pharmaceutical setting.

  • Hands-on experience with Argus or Argus J safety databases.

  • Proficiency in SQL and familiarity with reporting tools like OBIEE.

  • Experience configuring studies in safety systems.

  • Strong problem-solving and client service orientation.

  • Ability to identify and implement the best business solutions through technical insight.


About Medpace

Medpace is a full-service Clinical Research Organization (CRO) providing Phase I–IV clinical development services to the biotechnology, pharmaceutical, and medical device industries.
Our mission is to accelerate global development of safe and effective therapeutics through scientific discipline and operational excellence.

Headquarters: Cincinnati, Ohio
Global Presence: 40+ countries
Team Size: 5,000+ employees


Why Medpace?

People. Purpose. Passion. Make a difference tomorrow — join us today.

  • Over 30 years of impact in advancing global health.

  • Involvement in studies across oncology, cardiology, metabolic disease, CNS, antiviral, and more.

  • Work that contributes directly to improving patient outcomes.


Perks & Benefits

  • Flexible work environment

  • Competitive salary and benefits package

  • Generous PTO and structured career paths

  • Professional growth and training opportunities

  • Employee appreciation and wellness initiatives


Awards & Recognition

🏆 Forbes: America’s Most Successful Midsize Companies (2021–2024)
🏆 Life Science Leader Magazine: Multiple CRO Leadership Awards (Expertise, Quality, Reliability & Compatibility)


Next Steps

A Medpace team member will review your application. If shortlisted, you’ll be contacted for the next phase of the recruitment process.