Country Site Activation Internship - 6 months

IQVIAParis, Île-de-FranceOn-siteInternshipListed 5 hours ago

Apply now

About this role

Make an impact on patient health!

IQVIA’s Global Site Activation Team   of 2000 employees,   drive s   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.