Abogado/A En Badalona

Cronoshare.Com; Badalona; On-site; EUR 110,000 - 150,000; Full time

Job summary

IQVIA Biotech seeks a Senior Manager, Global Site Activation, Legal Liaison to provide expert operational support for clinical trial contracting when IQVIA is a contracting party. You will be a key contact for contracting matters, ensuring efficient issue resolution and alignment with internal legal requirements.

The role involves maintaining contract templates, leading template development, and implementing standardized practices across site contracting teams.

Qualifications

• Master's degree in law required.
• 5+ years' demonstrable experience as a qualified lawyer.
• Experience in sponsor/CRO or pharma site contracting preferred.
• Solid knowledge of GCP/ICH and regulatory guidelines.

Responsibilities

• Provide study-specific contracting support to PMs, SSUMs, Site Contract Negotiators, and Global Template Developers.
• Serve as the primary operational contact for complex contracting issues and escalate to Legal as needed.
• Advise stakeholders on approved contracting positions, templates, and IQVIA contracting policies.
• Own and maintain the Global Site Contracts Library and country-specific templates.
• Lead development, validation, and translation coordination of contract templates with version control.
• Ensure consistency with IQVIA Legal guidance and update contracting practices across the site 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.
• Support evolution of contracting processes and tools to meet changing business and country requirements.

Skills

Negotiation

Communication

Legal writing

Project coordination

GCP/ICH knowledge

Education

Master's degree in law

Job description

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

Sofia, Bulgaria
Belgrade, Serbia
Vienna, Austria
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Zaventem, Belgium
Madrid, Spain
Full time
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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

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 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.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

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