Safety System Administrator (Required Argus Safety Systems, system configuration and safety data migration experience)

Posted Yesterday
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Hiring Remotely in Pune, Mahārāshtra, IND
In-Office or Remote
Entry level
Biotech • Pharmaceutical
The Role
Administer Argus Safety databases, including configuration, library maintenance, upgrades, validation, change control, and legacy data migration. Provide user access management, troubleshooting, training, database outputs, case-processing metrics, and quality compliance support. Collaborate with clients, project teams, IT, and vendors on data-handling guidelines, software fixes, business continuity testing, and system improvements.
Summary Generated by Built In
Company Description

Medicine moves forward here. So will you. 

At PrimeVigilance, patient safety is not one part of the job. It is why we exist. 

We are a global pharmacovigilance specialist. Our teams help clients navigate complex regulations while keeping patient safety at the center of every decision, from early development through to post-marketing surveillance. Increasingly, the value we create is not only in processing safety data but in interpreting it: spotting the signal that matters early and turning it into insight our clients can act on. 

That work takes curious minds, problem-solvers and experts who care about getting it right. It also takes a culture worth staying for. Across Europe, North America, South America, Asia and Australia, we work in an environment built on kindness, flexibility, growth and belonging, where colleagues support one another and good ideas are heard wherever they come from. 

If you want a role with real purpose, global reach and the chance to keep growing while you help protect patients, you will feel at home here. We would love to hear from you. 

Job Description

Position Summary
This role requires working as part of the Safety & MI System Administrator Team performing database administration activities; supporting creation and upgrade of database instances; change control and data migration activities; first line user support and troubleshooting; and training users on databases.
 

Principal Responsibilities
The Safety System Administrator is primarily responsible for:
• Maintenance of database libraries
• Involvement in system validation activities
• Interrogating the database and generating outputs for internal and client use
• Training and providing database access to internal and client users

Principle Functions For the Client (may include but is not limited to the following)
• Set up and maintenance of project specific database libraries including:
         o Products 
         o Licenses
         o Studies
         o Reporting destinations 
• Documenting and validating any change to the project specific database
• Support during legacy data transfer e.g., validation
• Supporting/providing guidance to the Project Manager / Client / Project Start Up Team during the development of project specific data handling guidelines (to ensure project specific guidelines are necessary and will not impact line listings and report generation)
• Prepare line listings and tabulations and other database outputs for use in aggregate reports, signal detection, reconciliation and other activities as required
• Provide case processing metrics required for invoicing (e.g., number of submissions, number of spontaneous vs initial cases processed)
• Provide database training to clients
• Providing and documenting client / internal team access upon receipt of an approved access request.

For the Company (may include but is not limited to the following)
• Coordinate user access (including maintenance and revoking access)
• Maintain database procedures including core data handling conventions
• Provide database training and certification to PrimeVigilance users
• Provide user support
• Involvement in root cause investigation of database related deviations and ensure timely and complete documentation of resulting actions in line with Quality procedures
• Provide case processing quality and compliance metrics to the Quality Team
• Identify areas for improvement and address via training, clarifying changes to data handling guidelines, user guides etc.
• Execute business continuity periodic testing for database failure
• Ensure that existing software bugs, user requests, changes to regulatory requirements etc., are considered and appropriate changes are made and validated as required
• Support IT, database vendor and technical colleagues in troubleshooting and implementing software fixes and enhancements as required
 

Other Supportive Responsibilities
Assist PrimeVigilance senior management on an as needed basis. Potentially provide chargeable consulting / training activities to clients regarding Argus, and if required LSSMV.

Qualifications

Educated to degree standard

Demonstrated work experience within Argus Safety Systems.

Additional Information

When you join Ergomed Group, you make a difference by helping to bring safe and effective pharmaceutical treatment to patients around the world. You’ll join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting.  

We are diverse in many ways, yet our values unite us. Our values are how we work, not words on a wall. If they sound like you, you will feel at home here. 

  • Quality: we hold ourselves to the standard patients deserve. 
  • Integrity and trust: we do the right thing, especially when it is hard. 
  • Drive and passion: we care about the outcome, because someone is waiting on it. 
  • Agility and responsiveness: we move quickly, because patients cannot wait. 
  • Belonging: everyone is welcome, and every voice counts. 
  • Collaborative partnerships: we go further by going together. 

We look forward to welcoming your application.

Skills Required

  • Degree-level education
  • Demonstrated work experience with Argus Safety Systems
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The Company
HQ: London
535 Employees
Year Founded: 1997

What We Do

Founded in 1997, Ergomed is a global provider of high-quality services to the biopharmaceutical industry, spanning all phases of clinical trials, post-approval pharmacovigilance, and medical information. Ergomed’s fast-growing services business includes an industry-leading suite of specialist pharmacovigilance (PV) solutions, integrated under the PrimeVigilance brand, and Ergomed Clinical Research, a complete, global Phase I-IV clinical development and trial management services with a strong heritage in the development of drugs in rare diseases and oncology. • 1,400+ highly qualified professionals • Global full-service CRO • 25+ years of experience • Therapeutic specialization in oncology • Strong expertise in rare disease trials • Robust clinical safety system • Choice of leading drug safety databases Our key services include: • Clinical Research Services • Pharmacovigilance • Medical Information • Regulatory • Medical Writing • Site Management • Study Physician Support • Biostatistics • Patient Study Support

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