Global Medical Safety Intern

Johnson & Johnson • Full-time • US026 PA Spring House - 1400 McKean Rd, United States of America • 1w ago

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 https://www.jnj.com

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:

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.Our Oncology team is focused on the elimination of cancer by discovering new pathways and modalities to finding treatments and cures. We lead where medicine is going and need innovators with an unwavering commitment to results.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 http://www.jnj.com/innovative-medicine

Oncology Internship Program Overview:

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 forother opportunities at Johnson & Johnson (http://www.careers.jnj.com/students)upon successfully completing their degree program.The internship position is a full-time opportunityexpecting to last approximately 3 months(May 18 - August 14, 2026).

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.

Job Description

We offer an inclusive work culture that is open, innovative, and performance driven.As a summer intern in the Global Medical Safetyrole, you will be a member of a global matrixed 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 PhaseI to IIIclinical oncologystudies. The selectedcandidates will be assigned mentors and will have the opportunity to contribute to the project work within Global Medical Safety.This role may involve global team matrix interactions with colleagues from several different disciplines.

The OncologyGlobal Medical SafetyIntern may contribute to Cross-Functional Trial Team (CFTT) activitiesand may also collaborate with other project teams across various functional disciplines supporting various function specific projects.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. Students will have the opportunity to learn aspects of disease states, diagnosis,treatments, and the mechanism of action behind the emerging drugsbeing developed in conduct of our clinical trials. Students will also receive training onStandard Operating Procedures (SOPs),specific functiontraining, and related systems and tools.

Responsibilities may include:

Engagement in routine safety surveillance activities for clinical trial and post marketed data

Assist with planning and preparation for Periodic Safety Review (PSR) and Signal Management Team(SMT) meetings via thorough data review of cumulative and interval data

Contributions to efforts supporting any upcoming global submissions

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 broader knowledge of the drug development process and clinical research

Participating in department and team meetings

Participating in clinical and cross-functional team meetings

Collaboration with and/or assigned projects from other various functional disciplines

Leadership opportunities on specific internship program activities and/or group projects

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

Other projects as assigned

Qualifications

Legally/permanently authorized to work in the US 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

Graduate students in good standing, currently in a matriculated program and must be pursuing a master’s degree (Clinical Sciences, Clinical Research, Nursing, etc.), Physician’s Assistant, PharmD or PhD degreeor similar degrees

Undergraduate students in good standing with completion of at least six semestersenrolled in clinical,pharmacy,premed, physician’s assistant, nursing programs or similar areas of study will be considered

Self-motivated future scientists 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 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 key Microsoft suite of business tools including but not limited to Outlook, Excel, PowerPoint, Word, Teams, Slack, SharePoint, OneNote, etc.

Permanently authorized to work in the U.S., must not require sponsorship of an employment visa (e.g., H-1B or green card) at the time of application or in the future. Students currently on CPT, OPT, or STEM OPT usually requires future sponsorship for long term employment and do not meet the requirements for this program unless eligible for an alternative long-term status that does not require company sponsorship.

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 http://www.jnj.com/contact-us/careers or contact AskGS to be directed to your accommodation resource.

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