Country Site Activation Internship - 6 months

QPL IQVIA RDS Poland Sp. z o.o.; Paris; On-site; EUR 35,000 - 55,000; Full time

Job summary

IQVIA’s Global Site Activation Team is seeking an enthusiastic professional to support site activation and maintenance activities at country level. You will work under supervision as a SPOC, ensuring regulatory and SOP adherence while coordinating with SAM, PM and cross-functional teams.

Candidates should have a Life sciences degree and some clinical research exposure; 1–3 years' experience is desirable. This role offers growth in a global, data-driven environment within Paris and beyond.

Qualifications

• Bachelor's Degree Life sciences or related field.
• Desirable training in clinical research or CRA school.
• Desirable 1-3 years clinical research or related experience.

Responsibilities

• Serve a single point of contact (SPOC) to perform site activation and maintenance activities per regulations and SOPs.
• Review documents for completeness and accuracy under supervision.
• Prepare and review site documents for completeness.
• Inform team members of completion of regulatory and other documents for individual sites.
• Distribute completed documents to sites and project teams.
• Update and maintain internal systems, databases and timelines with project data.
• Review, track and follow up on progress and approvals for regulatory, ethics, and ICF documents.

Skills

Clinical research

Documentation

Regulatory knowledge

SPOC coordination

Education

Bachelor's Degree Life sciences

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. 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 Responsibilities

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 youre career! Unleash the 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.

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.