Iqvia Biotech
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OverviewIn this role you will provide expert operational support for clinical trial contracting when IQVIA is a contracting party.
You will act as the main contact for complex contracting issues, aligning practices with internal legal guidance and organizational requirements.
You will maintain and improve the global contract library and templates, and deliver training to Site Contracts teams.
You will work cross-functionally to drive standardization, governance, and compliant contracting processes.
This position offers impact across sites and countries with a focus on efficiency and risk mitigation.
ResponsabilidadesProvide study-specific contracting support to Project Managers, SSUMs, Site Contract Negotiators, and Global Template Developers
Serve as the primary operational contact for complex contracting issues and facilitate timely resolution, escalating to Legal Department as needed
Advise stakeholders on approved contracting positions, templates, and IQVIA contracting policies
Own and maintain the Global Site Contracts Library, including country-specific templates, guidance documents, and materials
Lead development, validation, maintenance, translation coordination, version control, and continuous improvement of contract templates
Ensure consistency with IQVIA Legal guidance and implement updated contracting practices across the site contracting team
Deliver training and ongoing support to Site Contracts teams on templates, processes, governance, and escalation procedures
Collaborate cross-functionally to drive standardization, operational excellence, and compliance in contracting activities
Support evolution of contracting processes and tools to meet changing business and country-specific requirements
Requisitos principalesMaster's degree in law
5 years' relevant sponsor or CRO contracting experience, including demonstrable EU Legal contract expert experience
Preference for pharmaceutical and/or CRO environment exposure
Strong negotiating and communication skills with ability to challenge
Ability to coordinate and collaborate across complex projects
Excellent legal, financial and/or technical writing skills
Thorough understanding of regulated clinical trial environment and knowledge of drug development process
Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines
negotiation
clear communication
cross-functional collaboration
contract templates and governance
legal writing
GCP/ICH regulatory knowledge
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