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

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.

Requirements:

• Master’s degree in law and demonstrable experience as a qualified lawyer

• 5 years’ relevant sponsor or clinical research organization, clinical site contracting experience, including demonstrable experience acting as an EU Legal contract expert

• 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

IQVIA 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 https://jobs.iqvia.com

IQVIA 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.

The potential base pay range for this role, when annualized, is zł201,500.00 - zł374,100.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.