Senior Clinical Data Manager

at Danaher Corporation in Richmond, Illinois, United States

Job Description

Leica Biosystems’ mission of “Advancing Cancer Diagnostics, Improving Lives” is at the heart of our corporate culture. We’re a global leader in cancer diagnostics with the most comprehensive portfolio from biopsy to diagnosis. Our easy-to-use and consistently reliable offerings help improve workflow efficiency and diagnostic confidence. Our associates know that every moment matters when it comes to cancer diagnostics. When you come to work, you’re helping develop solutions that enable accurate diagnoses to turn anxiety into answers. Join our diverse, global team of talented people, and be inspired to grow every day.

Leica Biosystems 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.

This position is part of the Biostatistics and Data Management in the Global Regulatory and Clinical Affairs and will be fully remote. At Leica Biosystems, our vision is to advance cancer diagnostics and improve lives.

You will be a part of the Biostatistics and Data Management team and report to the Director of Biostatistics and Data Management, responsible for leveraging the Danaher Business System and tools in the timely and high-quality execution of a clinical data management strategy for pre-market and post-market trials. If you thrive in a collaborative and fast paced environment and want to work to build a world-class diagnostics organization-read on.

In this role, you will have the opportunity to:

+ Plan, implement, and manage clinical trials and influence study design and interpret results.

+ Define clinical trial protocols, standard operating procedures (SOPs) and case report forms (CRFs) for use in clinical trials operations.

+ Independently complete all data management activities related to the set-up, initiation, execution, and close-out of device clinical trials within defined study timelines

+ Lead communications with EDC vendors and their staff regarding database activities in all phases of the trials to ensure study quality and timely deliverables

+ Provide clinical data management support to the clinical team, study projects, and biostatistics team.

The essential requirements of the job include:

+ Bachelor’s or master’s degree in science or health care area

+ 5+ years of experience in developing and executing clinical data management procedures and thorough knowledge of clinical research.

+ Occasional travel up to 25%

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

+ Experience in in-vitro diagnostics (IVD), Pathology, and Companion Diagnostics clinical research

+ Demonstrated ability to explain complex or sensitive information to diverse audiences, including senior leaders

+ Excellent organizational skills and ambition to continuously improve together with the business

At Leica Biosystems 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 Leica Biosystems can provide.

The salary range OR the hourly range for this role is $105,000.00 to $125,000.00. 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 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. 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 (https://www.dol.gov/agencies/ofccp/posters) .

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.