IMM Clinical Scientist Intern

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. Job Function: Career Programs Job Sub Function: Non-LDP Intern/Co-Op Job Category: Career Program All Job Posting Locations: Spring House, Pennsylvania, United States of America

Job Description
Immunology Clinical Scientist Intern 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 We are looking for the best talent in Immunology. Internship Program Overview The Johnson & Johnson Immunology Internship Program offers a full‑time, immersive learning experience within Immunology Therapeutic Area Research and Development. Interns contribute to meaningful projects, engage with leaders and colleagues across functions, and build practical skills through structured learning, mentorship, and exposure to the drug development process. The program is designed to foster professional growth while giving interns an opportunity to support innovative immunology research and clinical development. Designed to cultivate the next generation of talent, the program helps interns develop scientific, technical, and professional capabilities while exploring career opportunities in the pharmaceutical industry. The internship spans approximately three months, from May 17 through August 6, 2027. The position is located in Spring House, PA.

Job Description
As a Clinical Scientist Intern, you will join a clinical development team within the Immunology Therapeutic Area. With guidance from an assigned mentor, you will contribute to clinical trial activities and gain exposure to the development and implementation of clinical strategies across Phase I–III immunology studies. The role offers opportunities to collaborate with colleagues across scientific, medical, operational, regulatory, and other functional disciplines in a global matrix environment. The Clinical Scientist Intern may support cross‑functional trial team activities such as protocol and study‑material development, literature reviews, medical review of clinical data, clinical study report preparation, and documents supporting regulatory filings. In collaboration with the Study Responsible Scientist, Study Responsible Physician, and other team members, the intern may also help monitor or support aspects of clinical trial conduct. Each intern will complete one primary research project and may receive additional assignments based on team needs. Interns will present their work to project teams and conclude the program by presenting a poster or abstract on their primary project at the research symposium. The internship is designed to give undergraduate and graduate students practical experience in a large pharmaceutical research and development environment and a foundational understanding of novel drug development. Interns will learn about immune‑mediated diseases, including disease biology, diagnosis, treatment approaches, and the mechanisms of action of investigational medicines evaluated in clinical trials. The curriculum also includes training on applicable Standard Operating Procedures, study‑specific requirements, clinical database systems, and medical data review tools. You will be responsible for: 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 Developing study training materials/documents Shadowing key clinical and or functional roles for learning/development opportunities Supporting Clinical Team with study start