IQVIA Biotech

ppThe Sr Manager, Global Site Activation, Legal Liaison is responsible for providing expert operational support and guidance for clinical trial contracting activities when IQVIA Biotech is a contracting party. This role serves as a key point of contact for contracting matters, ensuring efficient issue resolution, consistency in contract practices, and alignment with internal legal and organizational requirements. /p h3Key Responsibilities /h3 ul liProvide study-specific contracting support to Project Managers, SSUMs, Site Contract Negotiators, and Global Template Developers. /li liAct as the primary operational contact for complex contracting issues and facilitate timely resolution while escalating legal matters internally to Legal Department as appropriate. Note: this position is not an in-house legal in legal department /li liAdvise stakeholders on approved contracting positions, templates, and IQVIA contracting policies. /li liOwn and maintain the Global Site Contracts Library, including country-specific contract templates, guidance documents, and supporting materials. /li liLead the development, validation, maintenance, translation coordination, version control, and continuous improvement of contract templates. /li liEnsure consistency with IQVIA Legal guidance and implement updated contracting practices across site contracting team. /li liDeliver training and ongoing support to Site Contracts teams on templates, contracting processes, governance, and escalation procedures. /li liCollaborate cross-functionally to drive standardization, operational excellence, and compliance in contracting activities. /li liSupport the evolution of contracting processes and tools to meet changing business and country-specific requirements. /li /ul h3Experience /h3 ul liMaster's degree in law and a minimum of 5 years' demonstrable experience as a qualified lawyer, preferably in a Law firm or as an In-House Legal Counsel. /li li5 years' relevant sponsor or clinical research organization (CRO) or with Pharma Clients, preferably in clinical site contracting /li liPreference, exposure to pharmaceutical and/or CRO environment /li liStrong negotiating and communication skills with ability to challenge /li liAbility to coordinate and collaborate across and within complex projects /li liExcellent legal, financial and/or technical writing skills /li liThorough understanding of regulated clinical trial environment and knowledge of drug development process /li liKnowledge and ability to apply GCP/ICH and applicable regulatory guidelines /li /ul pIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at /p pIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. /p /p