Sr. Manager, Clinical Science

Radiometer

United States

Remote

USD 170,000 - 190,000

Full time

14 days+
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Benefits offered by this job

Medical/dental/vision insurance
401(k) plan
Paid time off
Remote work arrangement

Job summary

Leica Biosystems, a Danaher operating company, seeks a Sr. Manager, Clinical Science (Global - Remote) to lead global clinical strategies and mentor a team of clinical scientists.

You will shape study designs for Digital Pathology, IHC/ISH, CDx and medical devices with cross‑functional partners across R&D, Regulatory, Medical Affairs and QA. This role emphasizes regulatory‑compliant study design, data interpretation, and publication-ready results, with strong leadership and collaboration across

Qualifications

  • Bachelor’s degree in Life Sciences, Healthcare, or related field with 12+ years in clinical research.
  • Masters/Doctoral degree with 10+ years in clinical research preferred.
  • Strong leadership and ability to guide clinical scientists.
  • Deep understanding of US/EU trial design and regulatory expectations.

Responsibilities

  • Oversee global clinical trial strategies for Digital Pathology, IHC/ISH, CDx and Medical Device.
  • Lead cross-functional teams with R&D, Regulatory, Medical Affairs and QA.
  • Ensure regulatory submissions support with robust clinical study data.
  • Mentor and develop a high‑performing team of clinical scientists.
  • Collaborate with CROs and investigators; communicate findings internally.

Skills

Leadership
Clinical trial design
Regulatory compliance
Cross-functional collaboration
Data interpretation
Mentorship
Scientific rigor
Strategic planning
Communication

Education

Bachelor's degree in Life Sciences
Master's or Doctoral degree

Job description

Sr. Manager, Clinical Science (Global - Remote)

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Leica Biosystems, one of Danaher's 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. At Leica Biosystems, we're not just shaping the future of cancer diagnostics - we’re transforming lives. Our mission of "Advancing Cancer Diagnostics, Improving Lives" is the driving force behind everything we do. As a global leader with the most comprehensive portfolio spanning from biopsy to diagnosis, we empower clinicians with innovative, reliable solutions so they can give patients timely, accurate answers when they need them most. When you join Leica Biosystems, you're not just taking a job; you're becoming part of a passionate team that knows every moment matters when it comes to cancer. You'll help develop diagnostic solutions that turn anxiety into answers, and aid the acceleration of next-generation, life-changing therapies. Surrounded by a diverse and collaborative global community, you'll be inspired each day to stretch, grow, and make an impact. Learn about the Danaher Business System which makes everything possible.

This leadership role is responsible for the oversight of all clinical trial strategies globally for Danaher Diagnostics. This role will specifically support Leica Biosystems, an operating company of Danaher Diagnostics. You will lead a team of clinical scientists, driving 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, Leica Biosystems organization and will be a remote role. 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:

  • Oversee the scientific planning and design of clinical studies for Digital Pathology, and Immunohistochemistry (IHC) & In Situ Hybridization (ISH), Companion Diagnostics (CDx) and Medical Device, ensuring scientific validity and alignment with overall clinical strategy.
  • Ensure the scientific rigor and accuracy of clinical protocols, case report forms, study reports, and other clinical documentation.
  • Serve as a key scientific liaison, working cross-functionally with R&D, Regulatory, Medical Affairs, and other teams to integrate clinical insights into product development and commercialization strategies.
  • Collaborate closely with Regulatory Affairs to support regulatory submissions and interactions with regulatory agencies by providing scientific expertise and clinical study data interpretation.
  • Build, lead, and mentor a high-performing team of clinical scientists, providing mentorship, guidance, and fostering their professional development to ensure high performance and scientific excellence.
  • Establish and maintain strong collaborative relationships with internal cross-functional teams (e.g., R&D, Regulatory Affairs, Medical Affairs, Quality Assurance, Data Management, Clinical Operations, Commercial) and external partners (e.g., CROs, investigators, key opinion leaders) to ensure successful clinical program execution.
  • Manage the analysis and interpretation of clinical study data, contribute to the preparation of regulatory submissions, and guide the dissemination of research findings through publications, presentations, and internal reports.

The essential requirements of the job include:

  • Bachelor's degree in Life Sciences, Healthcare, or a related field with 12+ years’ experience in clinical research, specifically with significant experience in US and/or EU trials, or a Masters or Doctoral degree with 10+ years of same experience.
  • 4+ years direct leadership experience, including experience managing clinical research scientists.
  • 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 leadership, communication (written and verbal) and interpersonal skills for managing a team and collaborating with cross-functional stakeholders.

It would be a plus if you also possess previous experience in:

  • Experience in study designs for in-vitro diagnostic technologies (IVD) is highly preferred, specifically for Digital Pathology and Immunohistochemistry (IHC) & In Situ Hybridization (ISH).
  • Advanced degree in Science, Healthcare, or Regulatory/Clinical Affairs.
  • Professional certification in Clinical Research (e.g., SoCRA, ACRP).

Leica Biosystems, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info. 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.

We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.

The annual salary range for this role is $170,000 to $190,000. 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.

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 We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.

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. For more information, visit www.danaher.com.

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. The U.S. EEO posters are available here.

For candidates who are based outside of New York City or who are applying for roles outside of New York City, for more information about conditions of any job offer please click here.

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: 1-202-419-7762 or applyassistance@danaher.com.

Danaher is a leading global life sciences, biotechnology, and diagnostics innovator, helping to solve many of the world’s most important health challenges, ultimately improving quality of life for billions of people today, while setting the foundation for a healthier, more sustainable tomorrow. The Danaher ecosystem is made up of more than 15 businesses united by a shared commitment to innovate for tangible impact.

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