Manager, Clinical Science & External Research
Company: Disability Solutions
Location: Irvine
Posted on: October 24, 2024
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Job Description:
Biosense Webster Inc. is recruiting a Manager, Clinical Science
& External Research (Scientific Communications) located in Irvine,
California. This role will work a hybrid schedule and must live
within a commutable distance to Irvine, CA to report to the office
on assigned days 2-3 times per week.The Manager, Clinical Science &
External Research (CSER) will be responsible for leading and
developing internal and external scientific communication contents
for assigned projects. We are looking for someone with high
standards of scientific analysis, teamwork, creative thinking, and
interpersonal skills for the advancement of clinical programs via
evidence generation and dissemination. You will collaborate closely
with a cross-functional team, including Scientific Affairs,
R&D, Health Economics, Marketing, and Education to conduct
literature reviews and gap analyses, lead strategic analysis of
scientific data, craft and implement comprehensive publication
plans, and support internal and external scientific communication
plans for various target audiences. In collaboration with
cross-functional teams and research investigators, you will
generate clinically relevant evidence for the company's innovative
pipeline that impacts patient lives. You will be joining a growing
function that drives research innovations! This role will have
broad reach and visibility with the Company.You should possess
advanced understanding and maintain current knowledge of industry
standards on scientific communication and publication development.
You will demonstrate understanding of the disease area, develop a
keen understanding of the Operating Company product portfolio and
clinical strategies to provide strategic input to publication
planning & evidence generation and dissemination strategies. We are
looking for a highly motivated and independent individual with
abilities to problem solve and run projects effectively. You are
expected to provide quality feedback and keep management informed
of key developments and issues related to your projects.You will
understand, incorporate, and follow all applicable laws and
regulations related to business activities, and Policies and
Procedures of Healthcare Compliance and Code of conduct. You will
serve as an internal subject matter expert on guidelines governing
the ethical publication of clinical study data, including mastering
the guidelines set forth by the International Committee of Medical
Journal Editors and Good Publication Practices, and applicable
policies governing compliant scientific communications.You may be
asked to provide training for employees, as needed. Additionally,
you may support associates that handle a variety of clinical
studies (investigator Initiated, registries, real-world evidence or
company sponsored post-market studies/premarket collaborative
studies) that collectively drive the generation of clinical
evidence for the Company's portfolio.You will consistently strive
to improve the performance, reputation, and image of the team and
ensure efficient use of resources to provide high quality
deliverables.Key Responsibilities:
Keywords: Disability Solutions, Florence-Graham , Manager, Clinical Science & External Research, Executive , Irvine, California
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