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Career Programs

Global Policy Summer Intern

  • Título Global Policy Summer Intern
  • Función Career Programs
  • Sub función Non-LDP Intern/Co-Op
  • Ubicación New Brunswick, New Jersey, United States
  • Publicado
  • Identificación requerida (Req ID) 2406167660W
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Descripción

At Johnson & Johnson, we use technology and the power of teamwork to discover new ways to prevent and overcome the world’s most significant healthcare challenges. Our Corporate, Medical Technologies, and Innovative Medicine teams leverage data, real-world insights, and creative minds to make life-changing healthcare products and medicines. We're disrupting outdated healthcare ecosystems and infusing them with transformative ideas to help people thrive throughout every stage of their lives. With a reach of more than a billion people every day, there’s no limit to the impact you can make here. Are you ready to reimagine healthcare? 

Here, your career breakthroughs will change the future of health, in all the best ways. And you’ll change, too. You’ll be inspired, and you’ll inspire people across the world to change how they care for themselves and those they love. Join us!     

Regulatory affairs (RA) is a profession developed from the desire of governments to protect public health by controlling the safety and efficacy of products in areas including pharmaceuticals, medical devices and consumer products among others, and by the companies responsible for the discovery, testing, manufacture and marketing of these products wanting to ensure that they supply products that are safe and make a worthwhile contribution to public health and welfare. 

Assignment Summary: 

The Global RA Policy Internship will provide graduate students the opportunity to develop practical experience in working with a public-private partnership. The Summer 2024 Internship will focus on supporting the IDERHA program (Integration of Heterogeneous Data and Evidence towards Regulatory and HTA Acceptance). IDERHA ( https://www.iderha.org ) is a European public-private partnership (PPP) launched in April 2023 between the European Union and the European life science industries that supports transformative research and innovation. IDERHA addresses the obstacles in accessing, integrating and analyzing health data to maximize their value for patient care and medical research. The intern may also support other Global RA Policy team activities.  

The IDERHA Internship Program will provide students with practical experience in public-private partnerships, working with cross-functional teams, while exposed to global regulatory and health technology assessment agency (HTA) policies.  

Responsibilities Include: 

  • Support the IDERHA policy team with a variety of complex activities in research, writing, and analysis of real-world evidence research and policies 

  • Conduct health policy-focused background research, drafting summary documents, performing literature reviews, contributing to a range of written deliverable types (e.g., policy briefs, white papers, blog posts, peer-reviewed publications) 

  • Contribute to a series of reports advancing policies that cover global health, health systems transformation, biomedical innovation, medical product development, real-world data and evidence, regulatory science, medical device and pharmaceutical policy, and the intersection of scientific and regulatory advancement  

  • Manage administrative tasks to support project work  

  • Synthesize and translate complex information from a wide range of inputs into clear and accessible written material for a range of audiences 

  • Prepare oral and/or written reports and analyses to present findings, establish progress, and analyze trends 

  • Support public and expert convenings (e.g., workshops, roundtables, seminars, other varied stakeholder meetings). 

  • Develop draft presentations and speaking points 

Calificaciones

Basic Qualifications: 

  • Education/Training: Currently enrolled in a graduate degree program in a relevant field (e.g., policy, public health, public administration, medical product regulation, economics, science, engineering, law, or field directly related to the position) is required 

  • Legal Authorization to work in the United States, without requiring sponsorship for employment visa status (e.g. H1-B status) now or in the future is required 

  • Ability to work full-time schedule in a virtual setting 

  • Excellent academic research, writing and professional communication skills 

  • Experience collaborating with a team  

  • Experience working in a detail-oriented project management support role desired  

  • Willingness to manage administrative duties and support senior staff project needs (e.g., meeting scheduling, note taking, task follow-up) 

  • Ability to exercise sound judgment and discretion, independently assess and resolve complex situations and shift priorities as the need arises 

Extended Qualifications: 

  • Problem solving and time management skills 

  • Experience developing graphic communications for data and research 

  • Ability to work independently with direction and the confidence to seek guidance when needed 

  • Experience within a healthcare setting and familiarity with medical product industry  

  • Proficiency with productivity tools including TEAMS and SharePoint 

  • Proficiency with Office 365  

  • Proficiency developing PowerPoint slides  

  • Handle confidential information in a professional and discrete manner 

The anticipated base pay for this position is Sophomore $21.00/hr, Junior $22/hr, Senior $23/hr, Master’s degree $29/hr.  

This job posting is anticipated to close on 03/12/2024.  The Company may however extend this time-period, in which case the posting will remain available on https://www.careers.jnj.com to accept additional applications.  

Johnson & Johnson is an Affirmative Action and 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, or protected veteran status and will not be discriminated against on the basis of disability. 

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