Intern Opportunity at IQVIA | Apply Now
The IQVIA Internship Madrid is a part-time, hybrid opportunity for aspiring professionals to gain hands-on experience in clinical trial start-up and site activation. Based in Madrid, Spain, it offers valuable exposure to the clinical research environment. Interested candidates should apply before the deadline.
- Position: Intern – Country Site Activation
- Location: Madrid, Spain (Hybrid)
- Duration: 6 Months/1 year
About IQVIA
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. The organization creates intelligent connections to accelerate the development and commercialization of innovative medical treatments to improve patient outcomes and population health worldwide. With a commitment to integrity and diversity, IQVIA fosters a culture of belonging among its employees.
IQVIA Internship Madrid: Job Description
This Country Site Activation internship involves supporting clinical trial start-up activities by assisting with regulatory, contractual, and document management processes. This role offers valuable exposure to the clinical research environment and site activation lifecycle.
Eligibility Criteria
- Bachelor’s or higher-level degree preferable in life science.
- Equivalent combination of education, training, and experience.
- Computer skills including working knowledge of Microsoft Word, Excel, and PowerPoint.
- Written and verbal communication skills – must be fluent in both English and Spanish.
- Effective time management and organizational skills.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
- Awareness of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.
- Knowledge of applicable protocol requirements as provided in company training.
What You’ll Gain
- Hands-on experience in clinical trial start-up and site activation.
- Exposure to regulatory and clinical research processes.
- Opportunity to develop professional skills within a global clinical research organization.
IQVIA Internship Madrid – Key Responsibilities
- Support the preparation and processing of contract addendums.
- Assist with regulatory submissions to relevant authorities and ethics committees.
- Prepare and track regulatory notifications.
- Support implementation and tracking of regulatory submissions and approvals.
- Conduct Trial Master File (TMF) reviews to ensure completeness and compliance.
- Maintain and update clinical trial systems and databases.
- Assist with administrative and operational site activation activities as required.
The IQVIA Internship Madrid presents a unique opportunity for candidates to enhance their skills and gain insight into the clinical research field. Qualified individuals are encouraged to apply before the deadline to seize this valuable experience.
