21 ago - Italia
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Experteer Overview In this role you design and analyze contracts for clinical trials, ensuring compliance and efficiency. You collaborate with crossâfunctional teams to assess risks and drive improvements, while maintaining accurate contract records. You will negotiate terms with clients and vendors, and provide guidance on interpretation and dispute resolution. This position supports ICON's mission to bring new medicines to patients faster by enabling robust, compliant contracting.
Retribuzione / Benefits Reviewing and analyzing contracts, agreements, and legal documents for clinical trial activities and vendor relationships
Negotiating contract terms with clients, vendors, and stakeholders to ensure regulatory compliance and policy alignment
Collaborating with crossâfunctional teams to assess contract risks and develop mitigation strategies
Maintaining accurate records of contract status, milestones, and deliverables in contract management systems
Providing guidance on contract interpretation, compliance, and dispute resolution to internal teams
ResponsabilitĂ Bachelor in business, life sciences, communications, or related discipline
3â5 years of experience in contract administration/management, preferably in pharma or clinical research
Strong understanding of contract law, legal terms, and regulatory requirements for trials and vendor agreements
Excellent analytical and problemâsolving skills with ability to handle complex contractual issues
Strong attention to detail, organizational skills, and ability to manage multiple tasks in a fastâpaced environment
Willingness to travel ~5%
Languages: Spanish and Italian
Requisiti fondamentali Competitive base salary
Health and wellbeing programmes (medical, dental, vision)
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities
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