Global Site Activation Leader

IQVIA; Madrid; Presencial; EUR 70.000 - 110.000; Jornada completa

Descripción de la vacante

IQVIA is seeking a Site Activation Manager in Madrid to lead start-up activities across global trials, coordinating with sponsors, sites and cross-functional teams to accelerate study delivery and regulatory compliance.

You will drive activation timelines, manage regulatory submissions and site contracting, while mentoring colleagues and contributing to process improvements in a fast-paced global environment.

Formación

• Bachelor's degree in Life Sciences or related field.
• Experience in site activation, study start-up, regulatory affairs or clinical operations.
• Strong knowledge of ICH-GCP and trial regulations.
• Experience managing timelines, budgets and cross-functional stakeholders.
• Excellent communication and stakeholder management skills.
• Ability to lead complex projects in a global environment.

Responsabilidades

• Lead site identification, feasibility, regulatory submissions and site contracting.
• Develop and execute Site Activation Management Plans aligned to study strategy.
• Drive study start-up timelines and milestones.
• Regulatory strategies, approvals and essential study documentation.
• Negotiate contracts and regulatory documents ensuring compliance.
• Mentor colleagues and contribute to continuous improvement.

Conocimientos

Site activation

Regulatory affairs

Cross-functional leadership

ICH-GCP

Stakeholder management

Project scheduling

Educación

Bachelor's degree in Life Sciences

Descripción del empleo

IQVIA is seeking a Site Activation Manager in Madrid to lead start-up activities across global trials, coordinating with sponsors, sites and cross-functional teams to accelerate study delivery and regulatory compliance.

You will drive activation timelines, manage regulatory submissions and site contracting, while mentoring colleagues and contributing to process improvements in a fast-paced global environment.