Intern GCO

Johnson Johnson; Madrid; On-site; EUR 10,000 - 12,000; Full time

Benefits offered by this job

6 months internship

Start March 2027

1000 € per month

Full time

Location: Madrid

Job summary

Johnson & Johnson in Madrid invites motivated students to join our Innovative Medicine internship program. As a Non-LDP Intern/Co-Op, you will support study planning, site start-up and execution activities, and contribute to trial documentation and regulatory submissions.

This full-time internship lasts six months, starts March 2027, and offers a 1000 € monthly stipend. English level B2-C1 is required, and you are pursuing a Master’s degree in clinical trial monitoring.

Qualifications

• English proficiency at B2-C1 level.

Responsibilities

• Study Planning Activities: country/site feasibility, trial documentation prep.
• Study Start Up: provide trial docs and materials, assist ECs and Health Authorities submissions.
• Study Execution: support drug distribution and maintain study files.
• Study Close Out: assist site closure and follow-up items.
• General Activities: ensure compliance with policies, train and update systems.

Skills

English B2-C1

Education

Master's degree in clinical trial monitoring

Degree in Pharmacy, Biology, Biotechnology, Biochemistry or similar

Job description

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com .

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Career Programs

Job Sub Function:

Non-LDP Intern/Co-Op

Job Category:

Career Program

All Job Posting Locations:

Madrid, Spain

Job Description:

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

What you will do:

1. Study Planning Activities

   Site Identification: Support the local study team in performing country and site feasibility

   Trial documentation: Support the preparation of study files and of any other document required pre-trial.

2. Study Start Up Activities / Site start-up

   Help LTM/SM in ensuring that the current versions of the required trial documents, trial-related materials and supplies are provided to the investigational site.

   Support the LTM or the SM in ECs and Health Authorities Submissions.

   Help the SM in obtaining site related trial documents.

   Support the LTM/SM in collecting and processing as appropriate the IFDF and related documents throughout the trial.

   Assist the LTM/SM in conducting local investigator meeting or in making arrangements for the investigators participating in an international meeting as applicable

   Help in the distribution, collection, reviewing, and tracking of regulatory documents, agreements and training documentation.

3. Study Execution Activities

   Support LTM/SM in drug distribution process, where applicable.

   Support LTM/SM in ensuring that during the trial all relevant trial related documentation is provided to investigators and central IEC (if applicable) within the timelines.

   Support the LTM/SM in maintaining the study files.

   Provide administrative and logistic support to LTM/SM in tracking of progress of the trial, management of study data, budget, organizing meetings, mailing and correspondence and other relevant tasks as appropriate, where applicable

4. Study Close Out Activities

   Site closure: Provide administrative and logistic support to the LTM/SM in activities related to study/site closure, as appropriate, and follow up of all items identified.

5. General Activities

   Base all actions on Credo. Protect the rights of others, protect privacy and company assets.

   Work in line with the HCC, company policies and procedures, including SOPs, having the ethical aspect in mind. Comply with ICH-GCP and all applicable local laws and regulations.

   Maintain communication with relevant parties within and outside the company

   Actively follow trainings to ensure adequate qualification

   Regularly update information in applicable systems and templates

   Contribute to maintain quality standards and timelines that are consistent with business needs

   Report every J&J product related complaint you receive to the company, according policies

Requirements

• Degree in Pharmacy, Biology, Biotechnology, Biochemistry or similar.
• Studying the Master's degree in clinical trial monitoring.
• English B2-C1.

We offer:

• Duration of the internship - 6 months
• Start date: March 2027
• 1000 € per month
• Full time
• Location : Madrid

The anticipated pay range and benefits for this position is: Dado que esta posición se publica en un pais sujeto a los requisitos de transparencia salarial de la EU, el equipo de Adquisición de talentos proporcionara información sobre el rango salarial a peticion y a los candidatos invitados a una entrevista.