Global Site Activation Lead

IQVIA; Lisboa; On-site; EUR 40,000 - 56,000; Full time

Job summary

IQVIA is seeking a Site Activation Specialist in Portugal to act as a single point of contact for feasibility, site activation and maintenance across studies, ensuring regulatory compliance and timely document management. You will review regulatory, ethics, and contract documents, coordinate with the Site Activation Manager and other teams, and maintain trial systems and timelines.

A Life Science degree and at least 3 years in Clinical Research are required; you should work well independently

Qualifications

• Bachelor’s degree in Life Science or related field.
• Minimum of 3 years’ experience in Clinical Research.
• Experience with ethics/regulatory submissions and site activation processes.
• Familiarity with global site activation responsibilities.
• Ability to work independently and with others.
• Strong interpersonal, communication and organisational skills.
• Ability to manage multiple projects.
• Knowledge of regulatory requirements including SOPs and ICH/GCP.

Responsibilities

• Serve as Single Point of Contact for feasibility, site activation and maintenance activities.
• Review regulatory and contractual documents and keep track of approvals.
• Distribute completed documents to sites and project teams; update systems and timelines.
• Monitor progress and ensure required documents (ethics, regulatory, CDA, etc.) are tracked.

Skills

Independent work

Team collaboration

Interpersonal skills

Organisational skills

Multitasking

Communication skills

Education

Bachelor’s Degree in Life Science or related field

Job description

IQVIA is seeking a Site Activation Specialist in Portugal to act as a single point of contact for feasibility, site activation and maintenance across studies, ensuring regulatory compliance and timely document management. You will review regulatory, ethics, and contract documents, coordinate with the Site Activation Manager and other teams, and maintain trial systems and timelines.

A Life Science degree and at least 3 years in Clinical Research are required; you should work well independently