Capability Development Specialist
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Job Description
Capability Development Specialist advancing trial data capabilities at ICON, a global healthcare intelligence and clinical research organisation. Leading stakeholder alignment, data maturity, quality, and roadmap delivery.
Responsibilities:
- Work with GDO, R&D and cross-functional stakeholders to elicit requirements and gain alignment for trial data capabilities defined by the Trial Data Delivery Strategy
- Build, develop and maintain collaborative working relationships with BPO/PEL and data initiative leads to deliver functional priorities in the trial data roadmap
- Provide leadership to advance trial data maturity and excellence in data quality
- Define functional capabilities for trial data capabilities in alignment with GDO business and strategic priorities
- Advise stakeholders on prioritizing requirements and ensure the total solution meets or exceeds customer expectations
- Execute and integrate small- to large-scale changes and requirements in project data delivery
- Use analytical approaches and independent judgment to identify and prioritize opportunities to streamline business processes
- Follow company and departmental policies, procedures, documentation, Takeda QMS, Software Development Life Cycle and Project Life Cycle standards
- Work independently with stakeholders to prioritize requirements and act as a primary resource on complex issues
- Establish relationships across Takeda, analyze issues, and guide solution development
- Build and maintain relationships with key business stakeholders
Requirements:
- Bachelor’s Degree or international equivalent preferred
- Advanced degree preferred
- 5+ years of experience in business analysis, data analysis, data transfer, data model roles or 6+ years relevant experience in lieu of bachelor’s degree or international equivalent
- 3+ years of experience in the life sciences preferred, with experience in clinical trial management/operations preferred
- Advanced understanding of the pharmaceutical industry, particularly clinical trial operations and trial management
- Understanding of GXP requirements, including 21CFR part 11 and validation methodologies
- Demonstrated skills to identify opportunities and anticipate changes in the business landscape through an understanding and ongoing assessment of the data environment affecting the business
- Experience with communication and presentation to cross-functional audiences
- Demonstrated ability to effectively work cross-functionally within a highly matrixed organization
- Legal right to work in the country where the role is based
Benefits:
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
- Benefits may vary depending on role and location
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