Clinical Research Associate (CRA)

Clinical Research AssociateAre 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 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.This position reports to the Manager, Clinical Site Operations and is part of the Global Clinical Affairs organization. The position will be fully remote within the United States.In this role, you will have the opportunity to:Oversee clinical study protocol execution at external sites, from start-up to close-out, ensuring timely data collection and compliance with FDA standards and Good Clinical Practice (GCP)Develop and maintain relationships with institutions, study investigators, internal stakeholders, and vendors to ensure successful trial execution, data integrity and adherence to project requirementsConduct study monitoring, including site coordination, investigational product accountability, and assessments of protocol deviations and/or adverse eventsManage IRB submissions and all study regulatory documentationContribute to study planning including budget and timeline forecasts, site identification and qualifications, and process improvement initiatives within the Global Clinical Affairs organization; as well as prepare study documents, including creating clinical templates, such as informed consent forms, clinical monitoring plan, etc.The essential requirements of the job include:Bachelor's degree with 2+ years clinical research experience OR Master's degree with 0-2 years clinical research experienceBasic knowledge of regulatory requirements and Good Clinical Practice for in vitro diagnostic and medical device productsPrevious experience with managing clinical research sites and monitoring clinical study dataGood technical background to understand and communicate current and new technologiesAbility to work on multiple projects simultaneouslyTravel, Motor Vehicle Record & Physical/Environment Requirements:Ability to travel 20-70%– including overnight(s), within the US. Travel may be up to 70% during project initiation periodsIt would be a plus if you also possess previous experience in:Retrospective/prospective biological sample procurementExperience with electronic Trial Master Files and Clinical Trial Management SystemsDemonstrated understanding of CLSI standards and their application to IVD clinical studies, including method comparison, precision/reproducibility, reference interval, specimen stability, clinical performance, and point-of-care evaluations.Within Danaher Diagnostics, we offer 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.Within Danaher 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.The annual salary range for this role is $85,000 - $95,000. 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.We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.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.