HomeBiotech JobsBS Clinical ResearchLife Sciences Internship at IQVIA, France | Clinical Research | Apply Now

Life Sciences Internship at IQVIA, France | Clinical Research | Apply Now

Life Sciences Internship at IQVIA, France | Clinical Research | Apply Now

Securing an internship at a top-tier clinical research organization is one of the most effective ways to launch a high-trajectory career in clinical operations. If you are a life sciences student or graduate looking for a premier Life Sciences Internship in France, IQVIA is offering a 6-month Country Site Activation Internship at their Courbevoie office. Operating in a flexible hybrid model, this position serves as an exceptional entry point into study start-up and trial maintenance. For those looking to secure a competitive Clinical Research Internship and explore a long-term IQVIA Career, here is a comprehensive, scannable breakdown of the role, your daily responsibilities, and the qualifications required.

  • Job Position: Country Site Activation Internship – 6 months
  • Location: Courbevoie, France
  • Job ID: R1546279

About The Company

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. The company utilizes unparalleled data, advanced analytics, cutting-edge technologies, and deep scientific expertise to drive healthcare forward. IQVIA’s Global Site Activation Team consists of over 2,000 employees across 141 locations worldwide, operating with a strict “patient-first” urgency to ensure clinical trials have access to safe and effective medications. As industry leaders in clinical innovation, they offer vast career development opportunities for early-career professionals looking to accelerate the development and commercialization of innovative medical treatments.

Life Sciences Internship – Key Responsibilities 

As a Site Activation Intern, you will work under direct supervision to execute site identification, regulatory submission, study start-up, and maintenance activities in accordance with global regulations, Standard Operating Procedures (SOPs), and country-level project requirements.

Your day-to-day operational and administrative duties will include:

  • Single Point of Contact (SPOC): Serving as a supervised point of contact to perform site activation and select maintenance activities for assigned investigative clinical sites, working closely with the Site Activation Manager (SAM) and Project Management teams.
  • Document Management: Preparing, reviewing, and checking essential site documents for completeness, consistency, and absolute accuracy under the guidance of senior staff.
  • System Updates: Updating and maintaining critical internal systems, databases, tracking tools, timelines, and project plans with accurate, study-specific information.
  • Milestone Tracking: Reviewing, tracking, and following up on the progress, approval, and execution of site questionnaires, Confidential Disclosure Agreements (CDAs), Ethics Committee submissions, Informed Consent Forms (ICFs), and Investigator Pack (IP) release documents.
  • Internal Communication: Informing internal project team members of the completion of regulatory or contractual milestones and distributing finalized documents to clinical sites.

Qualifications & Preferred Skills Required For Life Sciences Internship

This internship is tailored for highly organized, detail-oriented individuals with a foundational knowledge of clinical trial structures.

  • Educational Foundation: A Bachelor’s Degree in Life Sciences or a closely related scientific field is required to qualify for this Life Sciences Internship.
  • Preferred Training: Specific specialized training in clinical research or completion of a Clinical Research Associate (CRA) school is highly desirable.
  • Experience Profile: While this is an internship, 1 to 3 years of clinical research exposure or other relevant administrative experience in a regulated setting is an asset, though an equivalent combination of education and training is fully considered.
  • Core Competencies: Strong organizational skills, a high attention to detail, and the ability to work collaboratively within a multi-disciplinary, vibrant team environment.

In summary, this 6-month Country Site Activation Internship at IQVIA is an exceptional gateway into the clinical research sector. By securing this position, you will master the foundational mechanics of study start-up, regulatory document tracking, and clinical site engagement within a world-class framework. If you hold a life sciences degree, possess a passion for healthcare innovation, and are ready to gain hands-on experience in France, apply today to secure this premier Clinical Research Internship and kickstart your IQVIA Career.

APPLY ONLINE HERE

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