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Contact Info
Alan O'Riordan
Life Science

+353873657522
[email protected]
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Details

Data Analyst - Setup and Implementation


Reference:AOORAEME-667428 Location: Cork
Cork City
Qualification:DegreeExperience:1-2 Years
Job Type:PermanentSalary: Not Disclosed
May be suitable for: Data Management, Database Administrator

Data Analyst – Setup and Implementation

Overview
The Management Team is currently looking for a customer focused and quality centric IRT Setup and Implementation colleague to join its new team in Cork. This individual will be an exceptional professional, who consistently exceeds expectations, thrives in a challenging and dynamic work environment, and will be an active contributor to our team.

Roles and Responsibilities include the execution of the study set-up process and ensuring the IRT is configured and functions according to approved customer requirements. This position requires strong collaboration with other business partners to ensure successful IRT execution and compliance.

Key Responsibilities

  • Consultation, study set-up and execution
  • Build and maintain effective business partnerships with clinical study teams and key functions
  • Understand system functionalities, including capabilities and limitations, for the company’s internal IRT.
  • Participate in Study Development Process to review study-specific protocol requirements and establish implementation timelines
  • Participate in all aspects of the System Development Cycle, including but not limited to: Strong understanding of study-specific system requirements
  • Executing the study set-up process from requirements approval thru implementation
  • Creating study-specific documents including clinical-trial site IRT user tools
  • Ensuring timelines are met according to agreed-upon system-need dates
  • Provide a validated study-specific IRT build that meets approved customer requirements
  • Ensure confidentiality and blinding is appropriately maintained at all times
Maintain Operational Excellence
  • Sustain a culture of quality and compliance.
  • Proactively identify ways to improve day-to-day activities and practices, and actively communicate opportunities to peers and leadership team
  • Participate in and/or support the implementation of local/divisional projects and other process improvement initiatives
  • Take proactive measures to avoid or reduce crises. When emergencies occur, identify root cause of issues and communicate countermeasures and lessons learned
  • Demonstrate excellent project management abilities and strong understanding of IRT processes.
  • Troubleshooting configuration and execution problems (which could include logging formal incidents), identifying root causes, and implementing solutions
Basic Requirements
  • Fluent in English
  • Self-motivated professional with excellent customer service and strong working/team building relationship skills
  • Proven interpersonal and communication skills
  • Demonstrates good judgment and is solution orientated
  • Ability to work independently and within a team environment
  • Strong organizational and multitasking capabilities
  • Attentive to details to ensure compliance and accurate reporting
  • Experience of working to tight deadlines
  • Flexibility in adapting to a non-routine and fast paced environment
Additional Preferences
  • Systems experience especially IRT and/or electronic data capture
  • Ability to managing multiple IRT study builds simultaneously
  • Experience with Clinical Trial Materials supply chain
  • Understanding of clinical development and roles
Education Requirements
  • Bachelor’s degree or higher

For additional information, please contact Alan O Riordan on +353 87 365 7522 / [email protected]