Clinical Programs Manager
Location:
Northeast
Responsibilities:
Develop clinical strategy
and clinical plans.
Design clinical study
protocols to match regulatory pathways, reimbursement strategies, and marketing needs
worldwide.
Supervise small team of CRAs
for site management.
Mange external clinical data
management organizations.
Coordinate trials in
partnership with global clinical affairs groups.
Manage completion of interim
and final study reports.
Build relationships with key
departments, including sales, marketing, reimbursement and R&D.
Build strong relationships
with key medical investigators.
Qualifications:
5-10 years experience in
management of clinical trials
Medical device experience
required
Excellent ability to work
across functions including marketing, reimbursement, clinical, regulatory and R&D
Self Starter
Exceptional interpersonal
skills
Team Player able to work
well with a variety of colleagues
Decisive and quick thinker
able to deal well with abstract concepts and handle ambiguity well
Excellent presentation
skills and ability to relate well to diverse audiences
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