Intern GCO

En Johnson & Johnson creemos que la salud lo es todo. Nuestra fuerza en la innovación en la atención médica nos permite construir un mundo en el que se eviten, traten y curen enfermedades complejas, en el que los tratamientos sean más inteligentes y menos invasivos, y las soluciones sean personales. A través de nuestra experiencia en Medicina Innovadora y MedTech, estamos en una posición única para innovar en todo el espectro de soluciones de atención médica de hoy para ofrecer los avances del futuro y afectar profundamente a la salud para la humanidad. Obtenga más información en jnj.com Guiados por nuestro Credo, en Johnson & Johnson somos responsables de nuestros empleados que trabajan con nosotros en todo el mundo. Proporcionamos un entorno laboral inclusivo donde cada persona es tratada como individuo. En Johnson & Johnson, respetamos la diversidad y la dignidad de nuestros empleados y reconocemos sus méritos. Función de trabajo: Career Programs Subfunção Trabalho: Non-LDP Intern/Co-Op Categoría de trabajo: Career Program Todas las ubicaciones de colocación de trabajo: Madrid, Spain Descripción del trabajo: 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 We offer: - Duration of the internship - 6 months - Start date: March 2027 - 1000 € per month - Full time - Location : Madrid Requirements - Degree in Pharmacy, Biology, Biotechnology, Biochemistry or similar. - Studying the Master's degree in clinical trial monitoring. - English B2-C1. Habilidades requeridas: Habilidades deseables: El rango salarial previsto y los beneficios para este puesto son: 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 petición y a los candidatos invitados a una entrevista.