Site Activation Specialist, France

IQVIA; France; Hybrid; EUR 45,000 - 60,000; Full time

Job summary

IQVIA in France is seeking a Site Activation Specialist to oversee development, review and rollout of Informed Consent Forms across studies and countries. You will partner with global and country teams, ensuring accuracy, compliance and timely delivery.

The role requires a life sciences background, 3+ years in clinical research in France, strong communication and project management skills, and fluency in French and English. Hybrid or homebased work model offered.

Qualifications

• Clinical research knowledge in France (ideally +3 years hands-on)
• Strong communication, negotiation and problem solving skills
• Ability to manage multiple projects
• Knowledge of ICH/GCP and regulatory requirements
• Previous experience handling submissions and/or site contracts in France
• Native French speaker with advanced English proficiency

Responsibilities

• Prepare site regulatory documents for multiple sites and studies.
• inform team of completion of regulatory and contractual documents.
• Distribute documents to sites and internal team members.
• Maintain project tracking tools, timelines and plans.
• Track progress and approvals of regulatory documents, ICF and IP release documents.

Skills

Clinical research knowledge

Regulatory knowledge

Communication & negotiation

Project management

Problem solving

French language proficiency

English proficiency

Education

Bachelor’s in Life Sciences or related field

Job description

# **Site Activation Specialist** **Location: France** **Work Model:** Hybrid or Homebased **Make an impact on patient health with IQVIA!** Join our Global Site Activation Team, a 2,000‐strong network driving high‐quality site activation and ensuring patients gain access to safe and effective treatments. We lead with innovation and offer exceptional opportunities for growth.## ## **Role Overview** As a **Site Activation Specialist** , you will oversee the development, review, and rollout of Informed Consent Forms across multiple countries and studies. You’ll partner with global and country teams, ensuring accuracy, compliance, and timely delivery.## **What You’ll Do*** Prepare site regulatory documents, reviewing for completeness and accuracy.* Inform team members of completion of regulatory and contractual documents for individual sites.* Distribute completed documents to sites and internal project team members.* Support the updating and maintenance of internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information.* Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents.## ## **What We’re Looking For*** Bachelor’s in Life Sciences or related field* Clinical research knowledge in France (ideally with +3 year hands-on experience).* Strong communication, negotiation, and problem‐solving skills* Ability to manage multiple projects* Knowledge of ICH/GCP and regulatory requirements* **Previous experience handling submissions and/or site contracts in France.*** Native French speaker with advanced English proficiency## ## **Why IQVIA?*** Work across 21 therapeutic areas* Global exposure in 141 locations* Access to innovative technologies* Collaborative, growth‐focused environment **Unleash your potential and help drive healthcare forward.**It takes passion to make the extraordinary possible for patients. Our culture of innovation and collaboration enables us to explore new possibilities and help improve health around the world.When you join our diverse, global team, you’ll harness the power of unparalleled data, advanced analytics, cutting-edge technologies, and deep healthcare and scientific expertise to drive healthcare forward.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.comIQVIA 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.