In Vitro Malaria Internship

• Monthly gross stipend of €900.00

• 8 hours per day, full-time

• 1-year scholarship

• 25 days of vacation throughout the year

• Free on-site cafeteria

• Internship location in Spain: Severo Ochoa, 2, Tres Cantos (Madrid)

• The fellowship includes enrollment in the CITIUS Professional Initiation Program (Autonomous University of Madrid)

📚 Training Objectives

• Preparation of regulated clinical documentation: Learn the preparation, review, and organization of regulatory documentation related to clinical trials, understanding the submission procedures to Research Ethics Committees (CEIm) and the Spanish Agency of Medicines and Medical Devices (AEMPS).

• Physical and digital document management: Acquire knowledge regarding filing systems, classification, updating, and traceability of clinical files in accordance with the quality standards of the Clinical Operations area.

• Participation in a personalized CITIUS training itinerary: Design, together with academic and corporate tutoring, a learning itinerary adapted to the participant's profile, integrating practical experience with the training provided by the Universidad Autónoma de Madrid within the CITIUS Program. According to the call, the academic plan includes passing the ECTS credits established to obtain the university-specific degree.

• Logistical monitoring of research products: Learn the procedures associated with the documentary and logistical control of clinical research products, understanding the supply and traceability circuits established in the studies.

• Updating of clinical-epidemiological databases: Apply the knowledge acquired during university training to the maintenance and review of clinical records and databases, respecting quality and confidentiality criteria.

• Training in clinical trial monitoring: Participate, under supervision, in activities to prepare monitoring visits alongside the Clinical Research Associates (CRA) team, collaborating in document review, preparation of follow-up reports, and understanding applicable quality standards.

• Legal and regulatory training: Understand the regulatory framework governing clinical trials, Good Clinical Practice (GCP), GSK's internal procedures, and applicable regulations through training activities provided by both the CITIUS Program and the company.

This position will give you the opportunity to participate in key activities for your development. Your responsibilities include:

• Integrate into the in vitro unit of Global Health Medicines R&D and support active projects in the malaria area.
• Plan and execute in vitro assays for the potency evaluation of compounds against different strains of P. falciparum in medium and high-throughput formats.
• Characterization of compounds: Determination of speed of action, drug resistance, and target identification.
• Collaborate in the development, optimization, and validation of new cellular assays.
• Operate plate readers, dispensers, washers, and other automated laboratory equipment.
• Work in a level 3 biosafety laboratory*, following safety procedures and quality standards.
• Process, analyze, and check the quality of experimental data using Excel, SVV, and Spotfire.
• Collecting data, preparing reports, and presenting experimental results for internal meetings.

• Problem-solving mindset and eagerness to learn
• Scientific curiosity and initiative to propose improvements in assays and processes.

IMPORTANT: Please note that all individuals interested in applying for this fellowship must complete 2 applications to be considered:

1) Via the LinkedIn link (GSK/ViiV Healthcare Platform)

2) Through the following Talentoteca: link: Clinical Trials Internship | GLAXOSMITHKLINE, S.A. | T/2026/50413

Biotechnology, Cell Biology, Data Quality, Following Instructions, Interpersonal Communication, Life Science, Listening Effectively, Molecular Biology, Proper Documentation, Scientific ResearchThis is a temporary internship opportunity focused on professional development. Any reimbursement, scholarship, allowance, or financial support will be provided in accordance with applicable local laws, regulations, and GSK site policies. More detailed information will be provided during the recruitment process.Se trata de una oportunidad de prácticas de carácter temporal, orientada al desarrollo profesional. Los gastos elegibles, así como las becas o tasas podrán ser reembolsados de acuerdo con la legislación local aplicable, la normativa vigente o la política del centro de GSK. Se proporcionará información más detallada durante el proceso de selección.