Senior Site Activation Specialist - Belgium

IQVIA LLC; Henegouwen; À distance; EUR 83 000 - 117 000; Plein temps

Résumé du poste

IQVIA LLC in Belgium is seeking a Freelance Senior Site Activation Specialist (home-based) to support country-level clinical trial start-up and site management. You will focus on EU-CTR compilation, regulatory submissions, ICF adaptations, and activation, coordinating with cross-functional teams.

The role requires 2–3+ years in site activation or clinical research, a Life Sciences degree, and fluency in Dutch or French and English.

Qualifications

• Based in Belgium with strong understanding of the local regulatory environment.
• 2–3+ years of experience in site activation, study start-up, or clinical research.
• Bachelor’s degree in Life Sciences or related field.
• Solid knowledge of clinical trial start-up processes and regulatory requirements.
• Experience managing site documentation and submission processes.
• Strong attention to detail and ability to manage multiple sites and timelines.
• Fluent in Dutch or French and English (written and spoken).

Responsabilités

• Act as the primary point of contact for assigned investigative sites.
• Execute feasibility, site identification, and site activation activities in line with SOPs, regulations, and project timelines.
• Prepare, review, and manage essential site and regulatory documents, ensuring completeness and accuracy.
• Maintain and update tracking tools, timelines, and internal systems with accurate project data.
• Monitor and report on site activation progress and performance metrics.
• Ensure compliance with ICH-GCP, local regulations and study requirements.
• Collaborate closely with Site Activation Managers, Project Management, and cross-functional teams.

Connaissances

Site activation

Regulatory submissions

Documentation management

Project coordination

Regulatory compliance

ICH-GCP

Formation

Bachelor’s degree in Life Sciences

Description du poste

Freelance Senior Site Activation Specialist – Belgium (Home-Based)

Location: Belgium (home-based) Contract type: Freelance FTE: 1.0 - full time Start: immediately Duration: around 6 month

About the Role

We are looking for a Freelance Senior Site Activation Specialist based in Belgium to support country-level clinical trial start-up and site management activities. This role focuses on EU-CTR compilation, submission documents, regulatory submissions, ICF adaptions, packages and activation.

Key Responsibilities

• Act as the primary point of contact for assigned investigative sites
• Execute feasibility, site identification, and site activation activities in line with SOPs, regulations, and project timelines
• Prepare, review, and manage essential site and regulatory documents, ensuring completeness and accuracy
• Maintain and update tracking tools, timelines, and internal systems with accurate project data
• Monitor and report on site activation progress and performance metrics
• Ensure compliance with ICH-GCP, local regulations and study requirements
• Collaborate closely with Site Activation Managers, Project Management, and cross-functional teams

Requirements

• Based in Belgium with strong understanding of the local regulatory environment
• 2–3+ years of experience in site activation, study start-up, or clinical research
• Bachelor’s degree in Life Sciences or related field
• Solid knowledge of clinical trial start-up processes and regulatory requirements
• Experience managing site documentation and submission processes
• Strong attention to detail and ability to manage multiple sites and timelines
• Fluent in Dutch or French and English (written and spoken)

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.

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.