Analyst Engineer

Job ID: 08811
Location: Wilmington, DE  [Hybrid]
Employment Type: Contract
Apply Now
Back to Search

Apply Now

Fill out the form below to submit your information for this opportunity. Please upload your resume as a doc, pdf, rtf or txt file. Your information will be processed as soon as possible.

(Word, PDF, RTF, TXT)
Apply Now
* Required field.

RxLogix Consultant

Location: Remote / Hybrid (as applicable)

Employment Type: Contract / Contract-to-Hire / Full-Time

Overview

We are seeking an experienced RxLogix Consultant to support the implementation, configuration, validation, and ongoing optimization of pharmacovigilance and drug safety solutions. The ideal candidate will possess a strong understanding of drug safety processes, system implementation, data migration, and regulatory compliance within the Life Sciences industry.

Responsibilities

  • Gather and analyze business requirements from Pharmacovigilance and Drug Safety stakeholders.
  • Configure and support RxLogix applications based on business and regulatory requirements.
  • Support data migration, mapping, and reconciliation activities from legacy systems.
  • Perform system validation, testing, and documentation, including IQ/OQ/PQ activities.
  • Conduct user training sessions, workshops, and go-live support.
  • Coordinate integrations with enterprise systems and external applications.
  • Troubleshoot system issues and support change requests and enhancements.
  • Collaborate with business, technical, and vendor teams to ensure successful project delivery.
  • Provide post-implementation support and continuous improvement recommendations.

Required Qualifications

  • Experience with RxLogix or similar Pharmacovigilance platforms.
  • Strong understanding of Pharmacovigilance (PV) and Drug Safety processes.
  • Experience with software implementation and system configuration.
  • Knowledge of SQL and relational databases.
  • Experience with system validation and testing methodologies.
  • Experience with data migration, mapping, and reconciliation activities.
  • Excellent communication, documentation, and stakeholder management skills.

Preferred Qualifications

  • Experience working within regulated Life Sciences, Pharmaceutical, or Biotechnology environments.
  • Familiarity with safety databases, regulatory reporting, and compliance requirements.
  • Experience integrating enterprise applications and third-party systems.
  • Knowledge of SDLC, CSV, and GxP practices.

Skills

  • Pharmacovigilance (PV)
  • Drug Safety
  • RxLogix
  • Business Analysis
  • System Configuration
  • SQL
  • Data Migration
  • Validation & Testing
  • Requirements Gathering
  • User Training
  • Life Sciences Technology

Apply Now
View All Jobs

Similar Jobs

Software Developer
Columbia, MD  [On-Site]
Our client is seeking Software Developers and DevSecOps Engineers with experience in modern software development, cloud technologies, Linux, automation, and CI/CD practices to support mission-critical systems in a secure, fast-paced environment....

Level 2 Network Consultant
DE  [Hybrid]
Our client is seeking a Network Administrator with strong hands-on experience in networking, Microsoft infrastructure, Active Directory, DNS/DHCP, virtualization, backup technologies, and network security who can work independently, support enterprise environments, and provide exceptional customer...

Enterprise Resource Planning Manager
Bethlehem, PA  [On-Site]
Our client is looking for ERP Manager that oversees ERP system development, customization, and business process enhancements to support internal operational requirements beyond core platform functionality....

Business Subject Matter Expert 3
Dover, DE  [Hybrid]
-...

Help Desk Analyst 3
Dover, DE  [Hybrid]
Our client is seeking a customer-focused Help Desk Analyst III to provide high-volume phone and remote support, troubleshooting technical issues, documenting incidents, and escalating complex problems in a fast-paced service desk environment....