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As a summer intern in the Immunology Clinical Scientist role, you will be a member of a clinical team dedicated to the research and development of oncologic therapeutics including, execution of clinical strategies; the clinical and operational implementation of complex compound programs in Phase I to III clinical immunology studies. The selected candidates will be assigned a mentor and will have the opportunity to contribute to clinical trials in our pediatric immunology group. This role involves extensive global team matrix interactions with colleagues from several different disciplines.

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 the Study Responsible Scientist (SRS), the Study Responsible Physician (SRP), and or other project teams in various functional disciplines in monitoring and or supporting various aspects of clinical trial conduct. Each intern will have their own or group assigned projects and will be expected to present their work to their project teams and 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 experience in working in a large pharmaceutical R&D setting and to gain basic understanding of the science and process of novel drug development. Students 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 in conduct of our clinical trials. Students will also receive detailed 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

• 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)

• 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

• Development of study training materials/documents

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

• Observing Site Initiation Visits (SIVs)

• Supporting Clinical Team with study start up activities during trial set up, and other study tasks during conduct, and close out

• 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

• Review of medical literature, related products, and new technologies

• Collaboration and or assigned projects from other various functional disciplines

• Leadership opportunities on specific program and or group projects

• Abstract/poster preparation and presentation at organization-wide research symposium

• Other projects as assigned

Qualifications

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

· Undergraduate college students with completion of a minimum of four semesters of B.A./B.S/B.S.N. or 4 of 6 years of a PharmD

· Currently enrolled in a biology, chemistry, pre-med, PharmD or nursing program

· Graduate students must be pursuing a master’s, PharmD or PhD degree

· Must have a minimum cumulative GPA of 3.0

· Fluent in written and spoken English

· Good verbal and written communication skills

· Good presentation skills; leading presentations to peers, project teams and senior leadership teams.

· Working knowledge and or experience using key Microsoft suite of business tools including but not limited to Outlook, Excel, PowerPoint, Word, Teams, SharePoint, OneNote, etc.

Push the boundaries of science to transform health—and your career.

Join us and advance life-changing treatments for people who need them most. At Johnson & Johnson, our focus is on improving global health equity and developing MedTech and pharmaceutical innovations that impact the future of health. Using AI and robotics to transform surgery or helping data scientists and clinicians formulate new ways to diagnose and treat disease, this work may sound like sci-fi, but it’s all science, all real, and could be your career. Whatever your background, skills, or career goals, there’s a place for you to help solve some of the world’s most pressing health challenges with us.

Accelerate your career while changing the world.

Each of our broadly-based family of companies offers an inclusive and empowering culture and employee benefits (like paid time off to volunteer, transgender-inclusive and same-sex partner health insurance coverage, and more) designed to help you live your best life, however you define it. And our best-in-class learning and development approaches, mentorship, and access to innovators across the world will help you grow your skills and reach your career goals. Because when you're at your best, nothing stands between you and your next breakthrough.