Janssen Research & Development, LLC, a member of the
Johnson & Johnson Family of Companies is recruiting for Regulatory Medical
Writing Summer Interns to support the Neuroscience, Oncology, and
Cardiovascular & Metabolism Therapeutic Areas and Established Products.
The Regulatory Medical Writing group comprises scientific
and regulatory experts who provide high-quality clinical documents in support
of Janssen products to address important unmet medical needs in oncology,
immunology, neuroscience, infectious diseases and vaccines, and cardiovascular
and metabolic diseases.
The Internship Program is focused on providing college
students with practical industrial scientific and clinical experience. This position works as a
member of a team under specific direction of a Regulatory Medical Writing manager
The Regulatory Medical Writing Intern has an opportunity to:
collaboratively with Regulatory Medical Writing staff
to the preparation of sound scientific/clinical documents in assigned areas
under direct supervision using established templates and guidelines
that sections conform to Janssen style and formatting guidelines
in ongoing project team meetings
exposed to various other functions within the larger Global Clinical
Development Operations group
support for conduct and reporting of clinical studies within neuroscience Regulatory
support for ongoing data transparency activities within oncology Regulatory Medical
Writing (ie, preparation of redaction proposal packages for publication by
European Medicines Agency in accordance with Policy 70)
support for Regulatory Medical Writing submission-related activities for
cardiovascular compounds as well as Regulatory Medical Writing safety
monitoring reports and submission activities for Established products.
must be enrolled in an accredited college/university and pursuing a Bachelor
degree or higher in biological science, medicine, or other health-related
must be available to work full-time (up to 40 hours/week) for 10 to 12 weeks
from May to August.
who have completed at least two years of college coursework will be considered.
must be legally authorized to work in the United States and not require
sponsorship for employment visa status (e.g. H1-B status) now or in the
leadership is required.
must be detail-oriented, highly organized and able to manage multiple tasks.
must have the ability to work individually (independently) as well as on a team.
need to be proficient with Microsoft Office, Word, Excel, and Power Point, and
have strong interpersonal,
oral and written communication skills. Additional technical competencies in
SharePoint and other information technology systems are highly desirable, as is
experience with PubMed databases and other literature databases.
with ability to interpret and organize scientific data or preclinical
laboratory experience are strongly preferred.
minimum G.P.A. of 3.0 is strongly preferred.
in campus/community service activities is desired.
are based in Titusville, NJ (neuroscience), Springhouse, PA (oncology), or
Raritan, NJ (cardiovascular & metabolism and established products) and
require the candidates to work on site.Primary Location
United States-New Jersey-RaritanOrganization
Janssen Research & Development, LLC. (6084)Job Function