Clinical Research Internship: Operations and Monitoring

GSK·Madrid, Spain

What they offer

  • €12,600 a year

    Gross, as stated in the ad.

  • Full-time hours

    Per the ad.

What they ask for

  • Have the right to work in Spain

    GSK doesn't mention sponsorship in the ad.

  • Speak native-level Spanish

    Listed as a requirement in the ad.

  • Work on-site in Madrid

    No relocation package mentioned.

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About the role

🏢About the Company and the Department

The intern will join the Clinical Operations area of GSK's Medical Department, where they will learn about the processes supporting clinical research and the coordination of national and international clinical studies.

During the training placement, and always under supervision, the intern will participate in activities related to document organization, procedure monitoring, coordination of clinical research activities, and knowledge of the applicable regulatory framework. They will also receive training provided by the Medical Operations unit, the different therapeutic areas, and other units within the Medical Department.

The training plan will enable the development of skills through supervised participation in activities such as:

  • Learning about the structure and functioning of the Clinical Operations area within an international biopharmaceutical company.
  • Learning the procedures that govern the development of clinical trials in accordance with national and international regulations.
  • Participating in the preparation and organization of documentation required for clinical research studies.
  • Becoming familiar with document management processes and the maintenance of regulatory files.
  • Learning how the management of clinical trial medication works within established procedures.
  • Understanding the process of preparing regulatory documentation for clinical studies.
  • Participating in learning the administrative coordination of contracts with research sites and collaborating entities.
  • Collaborating in the organization of scientific meetings, clinical research events, and scientific dissemination activities.
  • Learning administrative follow-up procedures and documentation related to external vendors.
  • Developing skills in preparing internal reports and corporate documentation.
  • Understanding the dynamics of collaboration with international teams and clinical research sites.
  • Observing the development of activities related to clinical trial monitoring by accompanying specialized professionals, including educational visits to hospital sites when applicable.

What we're looking for

Requirements:

  • C1 level of English.
  • Interest in clinical research and the pharmaceutical industry.
  • Organizational and learning skills.
  • Strong written and verbal communication skills.
  • Ability to work in multidisciplinary teams.

Education & certifications

🎓Candidate Profile

Final-year students (only pending their final degree project/thesis where applicable) or graduates in the following fields may apply:

  • Business Administration and Management
  • Pharmacy
  • Biology
  • Biotechnology
  • Chemistry

What you'll get

  • Monthly gross stipend of €900.00

  • 8 hours per day, full-time

  • Hybrid internship (semi-onsite)

  • 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)

Skills

Agile Thinking, Business Acumen, Clinical Development, Clinical Trial Designs, Clinical Trials Monitoring, Communication, Creativity, Decision Making, Fostering Collaboration, Good Clinical Practice (GCP), Influencing Without Authority, Pharmaceutical Industry, Time Management. This 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, current regulations, or GSK site policy. More detailed information will be provided during the recruitment process.

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases - to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we're committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

Should you require any reasonable adjustments or arrangements to support you during the recruitment process, specific to your individual needs, please contact us on [email protected].

Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels.

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

Additional information

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) Via the following link on Talentoteca: Administrative Support Internship - Clinical Operations | GLAXOSMITHKLINE, S.A. | T/2026/50451

You'll most likely need Spanish to apply.This job was automatically translated to English, .

About the company

GSK

GSK

Pharma

View company profile
International company
70000 employees