Intern GCO

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.

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

• 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.

• 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.

• 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

• 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.

• 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 

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