Country Site Activation Internship - 6 months

IQVIA Inc; Paris; On-site; EUR 52,000 - 76,000; Full time

Benefits offered by this job

Exposure across 21 Therapeutic Areas

Global team across 141 locations

Access to new technologies

Collaborative and vibrant environment

Job summary

IQVIA in Paris seeks a Site Activation Associate to execute site identification, regulatory start-up, and maintenance activities for clinical trials under supervision. You will review and prepare site documents, coordinate with the Site Activation Manager and PM teams, and maintain accurate project records.

Join IQVIA’s global Site Activation network to gain exposure across therapeutic areas and develop your career within a collaborative, innovative environment focused on patient health.

Qualifications

• Bachelor's degree in Life Sciences or related field; CRA training optional.
• Desirable 1–3 years in clinical research or related experience.

Responsibilities

• Perform site activation, regulatory, start-up, and maintenance activities under supervision.
• Review documentation for completeness and accuracy with senior staff guidance.
• Update internal systems and project plans with accurate site information.
• Track regulatory, ethics, CDA and ICF documents and site releases.

Education

Bachelor's Degree Life sciences or a related field

Job description

Make an impact on patient health!

IQVIA’s Global Site Activation Team of 2000 employees, drives best in class site and customer experience, with industry leading outcomes.

Make an impact on patient health!

IQVIA’s Global Site Activation Team of 2000 employees, drives best in class site and customer experience, with industry leading outcomes.

We keep the patient at the forefront; ‘Always Impatient for the Patient’ and we excel in our collaboration with our external/internal customers.

IQVIA’s Country Site Activation team are a global network who identify and activate sites to the highest quality to ensure patients on Clinical trials have access to safe and effective medication.

We are leaders in innovation and first to new technologies, meaning a vast amount of career development opportunities are available.

Job Overview

Under supervision, executes the site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at country level.

Job Responsbilities

• With supervision, serve a Single Point of Contact (SPOC) to perform site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Site Activation Manager (SAM), Project Management team, and other departments as necessary. Review documents for completeness, consistency and accuracy, under guidance of senior staff.
• Prepare site documents, reviewing for completeness and accuracy.
• Inform team members of completion of regulatory contractual. and other documents for individual sites.
• Distribute completed documents to sites and internal project team members.
• Update and maintain 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 required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents.

Qualifications

• Bachelor's Degree Life sciences or a related field. Desirable specific training in clinical research or CRA school.
• Desirable 1 - 3 years’ clinical research or other relevant experience; or equivalent combination of education, training and experience.

Join IQVIA and let’s create a healthier world together:

• Exposure across 21 Therapeutic Areas
• Be part of a global team who operate across 141 locations
• Exposure across a variety of studies and projects
• Access to new, innovative technologies
• Work within a collaborative and vibrant environment
• Own your career!

Unleash your potential!

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.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.