The Global Onco logy Intern ship 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 ( http://www.careers.jnj.com/students ) upon successfully completing their degree program. The i nternship position is a full-time opportunit y expecting to last approximately 3 months (May 1 8 - August 1 4 , 202 6 ).

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 tw ice a week.

Job Description

We offer an inclusive work culture that is open, innovative, and performance driven . As a s ummer i ntern in the Clinica l Scientist role, you will be a member of a clinical team dedicated to the research and development (R&D) of on cologic therapeutics . S elected 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 I ntern may contribute to C ross- F unctional T rial T eam (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 provid ing support (as needed) for preparation of relevant documents for regulatory filings. The intern may also collaborate with Study Responsible Scientist s (SRS) , Study Responsible Physician s (SRP) , and or other project team member s 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 O ncology S enior L eadership 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 state s , diagnosis, treatment s , 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.

Responsibilities may include:

• Gain ing overall understanding of clinical research and drug development including but not limited to Good Clinical Practices (GCPs), International Conference of Harmony (ICH) guidelines, and St andard O perating P rocedures (SO Ps)

• Attend “Bench to Bedside” Lecture Series to gain knowledge of the drug development process and clinical research

• Assist ing 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 )

• Participati ng in department and team meetings

• Participat ing in cross-functional team and clinical team meetings

• Develop ing study training materials /documents

• Shadow ing key clinical and or functional roles for learning/development opportunities

• Observ ing Site Initiation Visit (SIV) Meetings (if applicable for assigned projects)

• Support ing 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 )

• Assist ing with review and cleaning of clinical data (i.e., medical review), query generation and resolution

• Assist ing with interpretation, report ing, and prepar ation of oral and written results of product research, in concert with senior clinical personnel, in preparation for health authority submissions (if applicable)

• Review ing 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/ p oster preparation and presentation at organization-wide annual research symposium

• Other projects as assigned