Clinical Affairs Scientific Study Manager
Company: Danaher Corporation
Location: Chicago
Posted on: May 8, 2024
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Job Description:
Wondering what's within Beckman Coulter Diagnostics? Take a
closer look.At first glance, you'll see that for more than 80 years
we've been dedicated to advancing and optimizing the laboratory to
move science and healthcare forward.
You could be just the right applicant for this job Read all
associated information and make sure to apply.
Join a team where you can be heard, be supported, and always be
yourself.
We're building a culture that celebrates backgrounds, experiences,
and perspectives of all our associates.
Look again and you'll see we are invested in you, providing the
opportunity to build a meaningful career, be creative, and try new
things with the support you need to be successful.Beckman Coulter
Diagnostics is proud to work alongside a community of six fellow
Diagnostics Companies at Danaher.
Together, we're working at the pace of change to improve patient
lives with diagnostic tools that address the world's biggest health
challenges. -The Clinical Affairs Scientific Study Manager for
Beckman Coulter Diagnostics is responsible for Managing the
In-Vitro Diagnostic Clinical Research for the Neurodegenerative
Disease Portfolio.This position is part of the Clinical Affairs
Department located in Chaska, MN and remote.
At Beckman Coulter, our vision is to relentlessly reimagine
healthcare, one diagnosis at a time.You will be a part of the
Clinical Affairs Team and report to the Senior Manager of Clinical
Affairs responsible for In-Vitro Diagnostic Clinical Research.
If you thrive in an innovative, dynamic role and want to work to
build a world-class Clinical organization-read on.In this role, you
will have the opportunity to:Design and lead early phase clinical
research focused on neurodegenerative disease clinical evidence
planning and portfolio development.Develop clinical strategy,
protocol design, case report form and informed consent
design.Manage clinical study timelines, resource demand and budget
across the disease portfolio.Develop internal and external
partnerships to ensure stakeholder satisfaction.Support good
clinical practice and scientific integrity concepts.Proactively
identify and resolve business challenges and/or regulatory
issues.The essential requirements of the job include:Bachelor's
Degree in field with 14+ years of experience or a master's degree
with 12+ years of experience or PhD/MD degree with 9+ years of
experienceExperience designing sponsored clinical studies for in
vitro diagnostic (IVD), pharmaceutical, or medical device.Advanced
knowledge of Good Clinical Practice and global IVD medical
deviceExperience developing regulatory strategy as it relates to
clinical study design and negotiating with regulatory agencies as a
subject matter expert.Experience in neurodegenerative disease
clinical researchIt would be a plus if you also possess previous
experience in:Experience working with external strategic
partners.Experience collecting real world evidence.At Beckman
Coulter Diagnostics we believe in designing a better, more
sustainable workforce.
We recognize the benefits of flexible, remote working arrangements
for eligible roles and are committed to providing enriching
careers, no matter the work arrangement.
This position is eligible for a remote work arrangement in which
you can work remotely from your home.
Additional information about this remote work arrangement will be
provided by your interview team.
Explore the flexibility and challenge that working for Beckman
Coulter Diagnostics can provide.The annual salary range for this
role is $150
- $200 K.
This is the range that we in good faith believe is the range of
possible compensation for this role at the time of this
posting.
We may ultimately pay more or less than the posted range.
This range may be modified in the future.This job is also eligible
for bonus/incentive pay.We offer comprehensive package of benefits
including paid time off, medical/dental/vision insurance and 401(k)
to eligible employees.Note: No amount of pay is considered to be
wages or compensation until such amount is earned, vested, and
determinable.
The amount and availability of any bonus, commission, benefits, or
any other form of compensation and benefits that are allocable to a
particular employee remains in the Company's sole discretion unless
and until paid and may be modified at the Company's sole
discretion, consistent with the law.At Danaher we bring together
science, technology and operational capabilities to accelerate the
real-life impact of tomorrow's science and technology.
We partner with customers across the globe to help them solve their
most complex challenges, architecting solutions that bring the
power of science to life.
Our global teams are pioneering what's next across Life Sciences,
Diagnostics, Biotechnology and beyond.
For more information, visit .Danaher Corporation and all Danaher
Companies are committed to equal opportunity regardless of race,
color, national origin, religion, sex, age, marital status,
disability, veteran status, sexual orientation, gender identity, or
other characteristics protected by law.
We value diversity and the existence of similarities and
differences, both visible and not, found in our workforce,
workplace and throughout the markets we serve.
Our associates, customers and shareholders contribute unique and
different perspectives as a result of these diverse attributes.The
EEO posters are available here.We will ensure that individuals with
disabilities are provided reasonable accommodation to participate
in the job application or interview process, to perform crucial job
functions, and to receive other benefits and privileges of
employment.
Please contact us at applyassistance@danaher.com to request
accommodation.Job SummaryJob number: R1260468Date posted :
2024-03-01Profession: ScienceEmployment type: Full time
Keywords: Danaher Corporation, Chicago , Clinical Affairs Scientific Study Manager, Healthcare , Chicago, Illinois
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