Abogado/A De Familia En Rubí

Cronoshare.Com; Barcelona; On-site; EUR 90,000 - 150,000; Full time

Job summary

IQVIA seeks a Senior Manager, Legal Counsel to provide study-specific contracting support and act as the primary operational contact for complex contracts across global sites.

The role requires a law degree with 5+ years as a qualified lawyer, experience in CRO/pharma settings, and strong negotiation/communication skills. You will maintain contract libraries, ensure policy alignment, and train Site Contracts teams.

Qualifications

• Master's degree in law and a minimum of 5 years' demonstrable experience as a qualified lawyer.
• 5 years' sponsor or CRO or Pharma client experience, preferably in clinical site contracting.
• Experience in pharmaceutical/CRO environments preferred.
• Strong negotiating and communication skills with ability to challenge.
• Ability to coordinate across and within complex projects.
• Excellent legal, financial and/or technical writing skills.
• Thorough understanding of regulated clinical trial environment and knowledge of GCP/ICH and regulatory guidelines.

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; escalate legal matters to Legal Department as appropriate.
• Advise stakeholders on approved contracting positions, templates, and IQVIA contracting policies.
• Own and maintain the Global Site Contracts Library including country-specific templates and materials.
• Lead development, validation, maintenance, translation coordination, and version control of contract templates.
• Ensure consistency with IQVIA Legal guidance and update 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 requirements.

Skills

Negotiation

Communication

Cross-functional collaboration

Legal writing

Regulatory knowledge

Education

Master's degree in law

Job description

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

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