OncoImmuno Clinical Scientist Intern

Johnson & Johnson • Spring House, PA

406d • Remote

About The Position

The OncoImmuno Clinical Scientist Intern position at Johnson & Johnson is a full-time internship designed for undergraduate and graduate students interested in oncology and immunology. This role provides a comprehensive learning experience in clinical research and drug development, allowing interns to contribute to clinical trials and gain exposure to various aspects of the pharmaceutical industry. Interns will work closely with clinical teams, participate in cross-functional activities, and present their research findings at a symposium at the end of the internship.

Requirements

• Legally authorized to work in the US with no required sponsorships.
• Currently enrolled in an accredited University or College program throughout the duration of the internship.
• Undergraduate students must have completed a minimum of four semesters.
• Student in good standing, working towards an undergraduate or graduate degree.
• Currently enrolled in a biology, cell/molecular biology, biochemistry, chemistry, pre-med, pharmacy, nursing program, or similar areas of study.
• Graduate students must be pursuing a master's, PharmD, PA, PhD, or other clinical-related degree.
• Self-motivated and 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 and senior leadership teams.
• Enthusiastic, collaborative, and able to build relationships 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.

Nice To Haves

• Experience in clinical research or drug development is a plus.
• Familiarity with clinical trial protocols and regulatory submissions.

Responsibilities

• Gain an overall understanding of clinical research and drug development including Good Clinical Practices (GCPs) and International Conference of Harmonization (ICH) guidelines.
• Assist with the management of trial activities including patient tracking and eligibility/enrollment reviews.
• Assist with document processing and management within the electronic master file (i.e., vTMF).
• Participate in department and team meetings.
• Participate in cross-functional team and clinical team meetings.
• Develop study training materials/documents.
• Shadow key clinical and/or functional roles for learning opportunities.
• Observe Site Initiation Visit (SIV) Meetings.
• Support Clinical Team with study start-up activities and other study tasks during conduct and close out.
• Assist with the review and cleaning of clinical data, query generation, and resolution.
• Assist with interpretation, reporting, and preparation of results for health authority submissions.
• Review medical literature, related products, and new technologies.
• Provide necessary training to local operational teams.
• Collaboration and/or assigned projects from various functional disciplines.
• Leadership opportunities on specific program and/or group projects.
• Prepare and present an abstract/poster at an organization-wide research symposium.
• Other projects as assigned.

Benefits

• Comprehensive learning experience in a leading healthcare company.
• Opportunity to work on real-world clinical trials and research projects.
• Exposure to various aspects of oncology and immunology drug development.

What This Job Offers

• Job Type: Full-time
• Career Level: Intern
• Industry: Chemical Manufacturing
• Education Level: Master's degree