Capability Development Specialist

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🇮🇳 India – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👻 Ghost score 10%

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ICON plc

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1990

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.

📋 Description

• 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