OncoImmuno Clinical Scientist Intern

e values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.

We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued, and our people can reach their potential.

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OncoImmuno Internship Program Overview:

The OncoImmuno Summer Intern 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 with diverse backgrounds who may pursue and apply for other opportunities at Johnson & Johnson ( https://https://www.careers.jnj.com/students) upon successfully completing their degree program. The i nternship position is a full-time opportunit y expecting to last 3 months (May 1 2 - August 15, 2025).

Based on business needs, internship positions may be available at various J&J locations throughout the US. Including, but not limited to New Jersey, Pennsylvania, Massachusetts, and California. We work on a "hybrid model" if you are NOT lab based. This means that you will be asked to report on site 3 times a week and can work remotely 2 times a week. If you are selected for an internship position, you will work directly with your manager as your start date approaches to confirm your exact schedule.

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 or immunologic 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 or immunology studies.

The Clinical Scientist intern 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 the 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 the Study Responsible Scientist (SRS), the Study Responsible Physician (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 or Immunology S enior L eadership Team (SLT), and are required to present their primary research project as a poster/abstract at the research symposium at 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 a basic understanding of the science and process of novel drug development. Students will have the opportunity to learn aspects of cancer or immunological 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 an 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)

• Assist ing with the management of trial activities including patient tracking through the 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

• Support ing Clinical Team with study start-up activities during the trial set up, and other study tasks during conduct, and close out.

• Assist ing with the 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.

• Review ing medical literature, related products, and new technologies.

• Providing necessary training to the local operational teams.

• Collaboration and/ or assigned projects from other various functional disciplines.

• Leadership opportunities on specific program and/ or group projects.

• Abstract/ p oster preparation and presentation at an organization-wide research symposium

• Other projects as assigned

Qualifications

• Legally/permanently authorized to work in the US with no required sponsorships

• Must be currently enrolled in an accredited University or College program throughout the duration of the internship

• Undergraduate college students must have completed a minimum of four semesters

• Student in good standing, working towards the completion of an undergraduate or graduate degree s

• Currently enrolled in a biology, cell/molecular biology, biochemistry, chemistry, pre-med, pharmacy or nursing program, or similar areas of study

• Graduate students must be pursuing a master's, PharmD, PA or PhD or other clinical-related degree

• Self-motivated, passionate about drug development and clinical research

• Proven leadership/participation with campus programs and/or service programs is desired

• Fluent in written and spoken English

• Great interpersonal, verbal, and written communication skills

• Good presentation skills; ability to lead presentations to peers, project teams, 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 us ing key Microsoft suite of business tools including but not limited to Outlook, Excel, PowerPoint, Word, Teams, Slack, SharePoint, OneNote, etc.

For additional general information on Company benefits, please go to: https://https://www.careers.jnj.com/employee-benefits

Johnson & Johnson is an Affirmative Action and 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, or protected veteran status and will not be discriminated against on the basis of disability.