we streven naar gelijke kansen voor iedereen en hanteren een competentiegerichte selectieprocedure. alle gekwalificeerde kandidaten zijn welkom, ongeacht leeftijd, seksuele geaardheid, nationaliteit, geloof, geslacht, handicap,...
klik op de "solliciteer nu" knop, maak je profiel aan en motiveer waarom jij de beste kandidaat bent voor deze job. tip: hou je profiel up-to-date, zodat je altijd snel kan solliciteren.
zo weet je dat wij met je sollicitatie aan de slag gaan. heel concreet bekijken we of jouw profiel beantwoordt aan de eisen van de job.
dan nemen we contact op. we overlopen samen je cv en de verdere stappen van je sollicitatie (gesprek, testing, referenties, rondleiding, ...)
we maken hem duidelijk waarom jij de geknipte kandidaat bent. zodra hij zijn feedback geeft - dat kan soms enkele dagen duren - brengen we je op de hoogte.
...en ben jij dat ook nog altijd? dan kan je het contract tekenen en is het tijd voor een feestje!
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volgende stappen
The Global Oncology Internship Program at Johnson & Johnson is a comprehensive learning and professional experience at one of the world’s leading health care companies. This program is designed to build a future pool of talent/candidates who may pursue and apply for other opportunities at Johnson & Johnson (https://www.careers.jnj.com/student ...
We work on a “hybrid model” if you are NOT lab based. This means that you will be asked to report on site three times a week and can work remotely twice a week.
We offer an inclusive work culture that is open, innovative, and performance driven. As a summer intern in the Clinical Scientist role, you will be a member of a clinical team dedicated to the research and development (R&D) of oncologic therapeutics. Selected candidates will be assigned a mentor and will have the opportunity to contribute to clinical trials. This role involves extensive global team matrix interactions with colleagues from several different disciplines and may provide exposure to the execution of clinical strategies and the clinical and operational implementation of complex compound programs in Phase I to III clinical oncology studies.
The Clinical Scientist Intern may contribute to Cross-Functional Trial Team (CFTT) activities, including but not limited to developing the clinical trial protocol, clinical trial materials, literature searches and review, medical review of trial data, coordinating completion of clinical study reports and providing support (as needed) for preparation of relevant documents for regulatory filings. The intern may also collaborate with Study Responsible Scientists (SRS), Study Responsible Physicians (SRP), and or other project team members in various functional disciplines in monitoring and/or supporting various aspects of clinical trial conduct. Each intern will have one primary research project and may have additional assigned projects as determined by the mentor and team. Interns will be expected to present their work to their project teams, the Oncology Senior Leadership Team (SLT), and are required to present their primary research project as a poster/abstract at the annual global summer intern research symposium towards the end of the internship.
The goal of this internship program is to provide undergraduate and graduate students with experience in working in a large pharmaceutical R&D setting and to gain basic understanding of the science and process of novel drug development. The intern will have the opportunity to learn aspects of cancer disease states, diagnosis, treatments, and the mechanism of action behind the emerging drugs being developed in our clinical trials. Students will also receive training on Standard Operating Procedures (SOPs) as part of the Clinical Scientist Intern curriculum, trial specific training, and the clinical database software and medical data review tool.
The Global Oncology Internship Program at Johnson & Johnson is a comprehensive learning and professional experience at one of the world’s leading health care companies. This program is designed to build a future pool of talent/candidates who may pursue and apply for other opportunities at Johnson & Johnson (https://www.careers.jnj.com/students) upon successfully completing their degree program. The internship position is a full-time opportunity expecting to last approximately 12 weeks (May 18 - August 14, 2026). Some flexibility is possible due to exams.
We work on a “hybrid model” if you are NOT lab based. This means that you will be asked to report on site three times a week and can work remotely twice a week.
We offer an inclusive work culture that is open, innovative, and performance driven. As a summer intern in the Clinical Scientist role, you will be a member of a clinical team dedicated to the research and development (R&D) of oncologic therapeutics. Selected candidates will be assigned a mentor and will have the opportunity to contribute to clinical trials. This role involves extensive global team matrix interactions with colleagues from several different disciplines and may provide exposure to the execution of clinical strategies and the clinical and operational implementation of complex compound programs in Phase I to III clinical oncology studies.
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The Clinical Scientist Intern may contribute to Cross-Functional Trial Team (CFTT) activities, including but not limited to developing the clinical trial protocol, clinical trial materials, literature searches and review, medical review of trial data, coordinating completion of clinical study reports and providing support (as needed) for preparation of relevant documents for regulatory filings. The intern may also collaborate with Study Responsible Scientists (SRS), Study Responsible Physicians (SRP), and or other project team members in various functional disciplines in monitoring and/or supporting various aspects of clinical trial conduct. Each intern will have one primary research project and may have additional assigned projects as determined by the mentor and team. Interns will be expected to present their work to their project teams, the Oncology Senior Leadership Team (SLT), and are required to present their primary research project as a poster/abstract at the annual global summer intern research symposium towards the end of the internship.
The goal of this internship program is to provide undergraduate and graduate students with experience in working in a large pharmaceutical R&D setting and to gain basic understanding of the science and process of novel drug development. The intern will have the opportunity to learn aspects of cancer disease states, diagnosis, treatments, and the mechanism of action behind the emerging drugs being developed in our clinical trials. Students will also receive training on Standard Operating Procedures (SOPs) as part of the Clinical Scientist Intern curriculum, trial specific training, and the clinical database software and medical data review tool.
Gaining overall understanding of clinical research and drug development including but not limited to Good Clinical Practices (GCPs), International Conference of Harmony (ICH) guidelines, and Standard Operating Procedures (SOPs)
Attend “Bench to Bedside” Lecture Series to gain knowledge of the drug development process and clinical research
Assisting with management of trial activities including patient tracking through screening process, and eligibility/enrollment reviews
Assisting with document processing and management within the electronic master file (i.e., vTMF)
Participating in department and team meetings
Participating in cross-functional team and clinical team meetings
Developing study training materials/documents
Shadowing key clinical and or functional roles for learning/development opportunities
Observing Site Initiation Visit (SIV) Meetings (if applicable for assigned projects)
Supporting Clinical Team with study start up activities during trial set up, and other study tasks during conduct, and close out (depending on the stage of the trial)
Assisting with review and cleaning of clinical data (i.e., medical review), query generation and resolution
Assisting with interpretation, reporting, and preparation of oral and written results of product research, in concert with senior clinical personnel, in preparation for health authority submissions (if applicable)
Reviewing medical literature, related products, and new technologies
Providing necessary training to local operational teams
Collaboration with and/or assigned projects from other various functional disciplines
Leadership opportunities on specific program activities and/or group projects
Abstract/poster preparation and presentation at organization-wide annual research symposium
Other projects as assigned
Legally/permanently authorized to work in Belgium with no required sponsorships. Curricular Practical Training (CPT) requirements must be communicated at time of application
Must be currently enrolled in an accredited University or College program throughout the duration of the internship.
Must not be graduating before, during, or after the start or end of the internship program
Currently enrolled in biology, cell/molecular biology, chemistry, pre-med, nursing program, public health, biochemistry, biomedical engineering, oncology, clinical pharmacology, clinical or translational research, computational biology, precision medicine, or similar areas of study
Undergraduate students with completion of a minimum of four semesters at program start or graduate students are eligible
Minimum cumulative GPA of 3.0 which is reflective of all college coursework
Students in good standing, working towards the completion of an undergraduate or graduate degrees
Graduate students must be pursuing a master’s, PharmD, Physician Assistant or PhD or other clinical related degrees
Self-motivated, future scientist leaders passionate about drug development and clinical research
Proven leadership/participation with campus programs and/or service programs is desired
Detailed oriented with good organizational skills
Possess strong leadership skills to participate and contribute to internship program initiatives and events
Fluent in written and spoken English
Great interpersonal, verbal and written communication and presentation skills
Ability to lead peers, project teams and present to project and senior leadership teams
Enthusiastic, collaborative, able to build relationships and work within global matrixed and cross-functional teams
Ability to work on and balance multiple project deliverables
Working knowledge and/or experience using Slack, Microsoft suite of business applications/tools including but not limited to Excel, OneNote, Outlook, PowerPoint, Sharepoint, Teams, and Word, etc.
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please contact us via https://www.jnj.com/contact-us/careers or contact AskGS to be directed to your accommodation resource.
We provide an allowance of €20 per worked day, to cover for your daily expenses. Additional support for housing opportunities is available depending on the distance to campus.
The candidate must be a registered student for the entire course of the internship. If you are interested in applying for this challenging internship, please send an e-mail to ra-rndbe-internbelg@its.jnj.com, including your resume and a short motivation.
Note: AN INTERNSHIP CAN ONLY START IF YOUR SCHOOL AGREES TO SIGN THE STANDARDIZED INTERNSHIP CONTRACT OF J&J BELGIUM. We cannot accept external contracts from the schools. Please, check this with your school BEFORE applying for an internship position.