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RTSM Technical Project Manager - Level I

£39.1 - £45.2 per hourEstimated
Full-time
Description

Key Accountabilities of the Technical Project Manager/Business Systems Analyst include the following:

System Implementation
  • Partnering closely with project leads in support of the implementation of configuration changes and to enable client start-up targets to 4G Clinical's PRANCER technology
  • Attend client meetings and design sessions as appropriate
  • Support logging, tracking and resolution of functional and technical issues discovered during implementation and prior to applying changes to production
  • Reviews and understands change impacts and risks with project leads to focus project testing efforts accordingly
  • Ensures adherence to required deliverables and milestones of Project Management SOP
  • Drive project specific validation activities including Build Verification Testing, Validation Testing, system setup and implementation activities.
  • Supports project validation activities including testing, setup, and implementation activities
  • Develops and executes scripts for testing
  • Supports changes to integrations, including implementing changes to integration specifications
  • Assist with client user acceptance testing (UAT) activities
System Operations
  • Serve as Customer Support point of escalation for any system or support issues where required; assist with creation of training materials.
  • Maintain issue logs for builds or validation activities of the RTSM.
  • Participate in client audits as needed.
This JOB description should not be deemed all-inclusive. Additional requirements and expectations may be assigned. At all times, employees are expected to adhere to company policies and company SOPs

Requirements

  • The position requires 1-3 years of experience in the clinical research field.
  • RTSM/IRT services delivery and eClinical systems implementation.
  • Software implementation and testing experience required in clinical research or supply chain related industry.
  • Project management experience working with cross-functional business and technical teams as project lead is required.
  • Knowledge of US FDA Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) GCP regulations, Electronic Records; Electronic Signatures regulation (21 CFR Part 11) and EU Annex 11 is a plus.
Education and/or Certification Requirements

The candidate must possess at minimum a bachelor's degree in a life science, supply chain management, or information technology field, or equivalent experience.
Vacancy posted 12 hours ago
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