Principal Clinical Scientist (Neurodegenerative)
Chaska, MN - USA
Job Summary
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences diagnostics and biotechnology
Within Danaher the work our diagnostic businesses do saves livesand were all united by a shared commitment to innovate for tangible impact.
Youll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danahers system of continuous improvement you help turn ideas into impact innovating at the speed of life.
Were accelerating the development of cutting-edge diagnostics to solve some of the worlds most pressing health challenges. Across our diagnostics operating companieswe are drivinginnovationthroughpartnerships with top academic institutions and leading players in biopharma and translational research.Were bringing the best minds together toaccelerateinnovation and unlock the full potential of the latest scientific advances. Together were expanding access to precision diagnostics for millions of people worldwide - and were using our unmatched global scale and proven playbook to make it happen from hospital labs to mobile clinics. By helping providers patients and families get faster more precise diagnostic results were improving treatment options and saving lives.
Learn about theDanaher Business Systemwhich makes everything possible.
Principal Clinical Scientist. This role is responsible for clinical trial strategies within the US and EU regions for Danaher Diagnostics Neurodegenerative program. This role will specifically support Beckman Coulter Diagnostics and Life Sciences operating companies of Danaher Diagnostics. You will drive strategic study designs ensuring regulatory compliance and achieving key milestones for critical clinical studies in these vital markets.
This position is part of the Danaher Diagnostics Beckman Coulter Inc. organization and will be remote based (can also be onsite in Chaska MN). At Danaher Diagnostics our vision is to be the leading provider of seamlessly connected diagnostic solutions.
In this role you will have the opportunity to:
- Design clinical studies and evidence strategies supporting global regulatory submissions (e.g. FDA 510(k)/PMA CEIVDR) across multiple diagnostic modalities.
- Act as a scientific and clinical liaison with regulatory bodies key opinion leaders and external sites to develop protocols claims and evidence plans.
- Partner crossfunctionally with R&D Regulatory Medical Affairs Quality and Commercial teams to align clinical programs with product development and market access needs.
- Author and review clinical and regulatory documentationincluding study reports technical files and publicationsto support product clearance and commercialization.
- Build strong internal and external collaborations mentor junior scientists and maintain expertise in evolving regulatory standards clinical guidelines and diagnostic technologies
The essential requirements of the job include:
- Bachelors degree in Life Sciences Healthcare or a related field with 9 years of experience in clinical research specifically with significant experience in US and/or EU trials or a Masters degree with 12 years of experience or Doctoral degree with 4 years of same experience.
- In-depth understanding of clinical study design and methodology in the diagnostics medical device or pharmaceutical industry with products intended for the US and EU markets.
- Demonstrated ability to identify and solve complex issues in clinical trial conduct and scientific interpretation.
- Ability to critically review and interpret scientific and clinical trial data and oversee the scientific aspects of study protocols and reports.
- Excellent communication (written and verbal) and interpersonal skills for collaborating with cross-functional stakeholders.
It would be a plus if you also possess previous experience in:
- Experience in study designs for diagnostic technologies (IVD) is highly preferred specifically for Neurodegenerative Biomarkers.
- Advanced degree in Science Healthcare or Regulatory/Clinical Affairs.
- Professional certification in Clinical Research (e.g. SoCRA ACRP).
Danaher Diagnostics a Danaher company offers a broad array of comprehensive competitive benefit programs that add value to our lives. Whether its a health care program or paid time off our programs contribute to life beyond the job. Check out our benefits at .
This job is also eligible for bonus/incentive pay.
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$120K-$130K.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. 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 Companys sole discretion unless and until paid and may be modified at the Companys sole discretion consistent with the law.
Join our winning team today. Together well accelerate the real-life impact of tomorrows 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.
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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.
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We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process to perform essential job functions and/or to receive other benefits and privileges of employment please contact:1- or .
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WHO WE ARE We are a global science and technology innovator committed to helping customers solve complex challenges and improving quality of life around the world. These are the moments that make a difference. Performing a delicate operation on an unborn baby. Minimizing waste at ever ... View more