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Title |
Location |
Type |
Rate |
Apply Now |
| Dir.
Medical Affairs, Pharmaceutical 2924 |
Rochester,
NY |
Perm/Full |
$143,000 -
$168,000 |
Submit Resume |
Director Medical Affairs,
Pharmaceutical
Job Description: Act as
thought partner to
marketing and R&D on
designing Clinical
Development Projects,
labeling, and
communications all
within compliance
parameters.
Takes an active role in
managing Phase IV
clinical programs
supporting both products
in development as well
as marketed product
globally.
Strong ability to
interpret and
communicate clinical
studies. Ability to
recommend, present and
defend appropriate
product claims,
scientific opinions and
interpretations for
products in prelaunch,
launch and post launch
phases.
The Medical Director
will play a major role
in developing the
research agenda for the
Company
categories and will be
an active contributor to
business plan.
Ability to lead direct
reports and oversee
large-scale projects.
Individuals in this
position collaborate
with internal
stakeholders, external
customers and key
thought leaders to
develop phase IIIb/IV
research initiatives,
and create clinical
education and support
programs.
Knowledge of Marketplace
medical trends and works
closely with the sales
and marketing group to
provide clinical input
for marketing
initiatives, sales
materials, education and
training. Industry
specific knowledge
medical & legal
regulations, procedures,
and practices that
impact the business.
Oversees scientific
communication planning
process, and coordinate
closely with the medical
education and CME
groups.
Ability to forge strong
external relationships
with KOLs, PBMs, and the
FDA.
Acts as a liaison
between company and
clinical investigators.
Develops credible
relationships with
opinion leaders, medical
directors, and key
regulatory officials.
Build functional
excellence by attracting
and retaining top
quality talent,
maintaining strong
external relationships,
and maintaining strong
internal lines to ensure
appropriate flow of
medical information.
Provides editorial
content and comments for
phase IV clinical study
reports & manuscripts.
Manages Phase IV
Clinical programs.
Qualifications
Education: MD/OD/PhD
with Opthalmic
experience.
Experience: 7- 10 years
in Ophthalmic industry,
Pharmaceutical Industry,
ideally as a clinical
leader. Demonstrated
experience with several
products, led through
clinical development,
regulatory approval, and
launch.
Work Location NY -
Rochester |
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