Affairs is the medical organization within Janssen’s US business that is
responsible for all medical aspects of life cycle management of approved drugs.
We work in conjunction with key internal Janssen stakeholders such as Health
Economics and Outcomes Research, Marketing, and Medical Communication and
external stakeholders such as health care providers and investigators, to
generate and disseminate medical information and to support the
commercialization of approved products. Scientific development and exchange,
and evidence generation are critical to these responsibilities. Strategic plans
for the upcoming year and the longer term future are developed each summer
through Integrated Evidence Generation Plan (IEGP) and Business Plan (BP) activities.
management group within USMA is responsible for driving the cross-functional
program execution of all operational activities related to the Immunology and
Oncology business units. These activities include project management support
for ongoing and
activities (e.g. Company Sponsored Trials and Interval Safety Reports).
Additionally, program management plays a critical role in the development of
the IEGP and BP strategic plans each summer.
The Oncology Medical Affairs Intern will:
- This individual’s primary role will be to assist with IEGP and BP
activities. This includes attending IEGP and BP meetings, preparation and
distribution of minutes and meeting summaries, and identification of action items
for all scheduled meetings.
- This individual will also assist the program manager and the
Therapeutic Area Lead in other USMA clinical projects and research activities,
such as the development and execution of clinical trials, post-marketing
commitments and strategic data gap analysis projects.
- This internship will
provide exposure to clinical strategy, data generation activities, and life
cycle management of approved drugs.
- Qualified candidates must be enrolled in a Bachelor, Masters or Doctoral
program in life sciences, medical sciences, chemistry, or business
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 (including a high
proficiency with generating pivot tables and graphs), and Power Point, and have
strong 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 academic and/or industrial clinical trial experience are strongly preferred.
- A minimum
G.P.A. of 3.0 is strongly preferred.
must have their own transportation
Janssen Scientific Affairs, LLC (6120)Job Function