IQVIA Biotech - Global Site Activation, Senior Manager, Legal Council

The 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.

Key Responsibilities

• Provide study-specific contracting support to Project Managers, SSUMs, Site Contract Negotiators, and Global Template Developers.
• Act 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
• Advise stakeholders on approved contracting positions, templates, and IQVIA contracting policies.
• Own and maintain the Global Site Contracts Library, including country-specific contract templates, guidance documents, and supporting materials.
• Lead the 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 site contracting team.
• Deliver training and ongoing support to Site Contracts teams on templates, contracting processes, governance, and escalation procedures.
• Collaborate cross-functionally to drive standardization, operational excellence, and compliance in contracting activities.
• Support the evolution of contracting processes and tools to meet changing business and country-specific requirements.

Experience:

• Master’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.
• 5 years’ relevant sponsor or clinical research organization (CRO) or with Pharma Clients, preferably in clinical site contracting
• Preference, exposure to pharmaceutical and/or CRO environment
• Strong negotiating and communication skills with ability to challenge
• Ability to coordinate and collaborate across and within 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