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Oncology Global Medical Safety Intern
Johnson & Johnson. Engage in routine safety surveillance activities for clinical trial and post-marketed data .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates a strong understanding of clinical research and drug development, including GCPs, ICH guidelines, and SOPs. Capable of engaging in safety surveillance activities and collaborating effectively within global matrixed teams.
Highest-signal resume keywords
Clinical ResearchDrug DevelopmentGCPsICH GuidelinesPresentation Skills
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Safety SurveillanceData ReviewProject ManagementAbstract PreparationSignal Management
Soft Skills
Self-MotivatedLeadershipOrganizational SkillsInterpersonal SkillsCommunication Skills
Tools & Technologies
Microsoft ExcelMicrosoft PowerPointMicrosoft WordMicrosoft OutlookMicrosoft TeamsMicrosoft SharePointSlack
Industry Keywords
Oncologic TherapeuticsClinical Oncology StudiesPeriodic Safety ReviewGlobal SubmissionsCross-Functional Teams
About the role
Key responsibilities & impact- Engage in routine safety surveillance activities for clinical trial and post-marketed data
- Assist with planning and preparation for Periodic Safety Review and Signal Management Team meetings through review of cumulative and interval data
- Support efforts for upcoming global submissions
- Gain understanding of clinical research and drug development, including GCPs, ICH guidelines, and SOPs
- Attend the “Bench to Bedside” Lecture Series
- Participate in department, team, clinical, and cross-functional team meetings
- Collaborate on projects with other functional disciplines
- Lead or participate in internship program activities and group projects
- Prepare and present an abstract/poster at the organization-wide annual research symposium
- Present work to project teams and the Oncology Senior Leadership Team
- Complete other projects as assigned
- Contribute to Global Medical Safety projects within a global matrixed team supporting oncologic therapeutics and clinical oncology studies
Requirements
What you’ll need- Legally/permanently authorized to work in the US with no required sponsorships
- Curricular Practical Training (CPT) requirements must be communicated at time of application
- 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 must be in good standing, currently matriculated, and pursuing a master’s degree, Physician’s Assistant, PharmD, PhD, or similar degree
- Undergraduate students must be in good standing and have completed at least six semesters in clinical, pharmacy, premed, physician’s assistant, nursing, or similar areas of study
- Self-motivated and 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
- Strong leadership skills
- Fluent in written and spoken English
- Strong interpersonal, verbal, written communication, and presentation skills
- Ability to lead peers, project teams, and present to project and senior leadership teams
- Ability to build relationships and work within global matrixed and cross-functional teams
- Ability to balance multiple project deliverables
- Working knowledge and/or experience using Slack and Microsoft business applications including Excel, OneNote, Outlook, PowerPoint, SharePoint, Teams, and Word
- Must not require sponsorship of an employment visa at the time of application or in the future
- Students currently on CPT, OPT, or STEM OPT generally do not meet requirements unless eligible for an alternative long-term status without company sponsorship
Benefits
Comp & perks- Hybrid work model: report on site three times a week and work remotely twice a week
- Full-time internship lasting approximately 12 weeks
- Assigned mentors
- Opportunity to present work to project teams and Oncology Senior Leadership Team
- Opportunity to present a primary research project as a poster/abstract at the annual global summer intern research symposium
- Training on Standard Operating Procedures (SOPs), specific function training, and related systems and tools
- “Bench to Bedside” Lecture Series
- Leadership opportunities on internship program activities and/or group projects
- Inclusive work environment
- Equal Opportunity Employer
- Interview process accommodations for applicants with disabilities