Job Overview
Location
USA - Remote
Job Type
Full-time
Category
Product Management
Date Posted
June 25, 2026
Full Job Description
đź“‹ Description
- • Oversee the end-to-end execution of IVD and medical device clinical trials at external clinical research sites and laboratories, ensuring compliance with FDA standards and Good Clinical Practice (GCP) from study start-up through close-out.
- • Independently train, manage, and monitor external clinical research sites to ensure protocol adherence, data integrity, and timely collection of clinical data.
- • Conduct site monitoring activities including investigational product accountability, assessment of protocol deviations, and follow-up on incomplete data entries or outstanding queries to maintain high-quality clinical data.
- • Manage all regulatory documentation for clinical trials, including IRB submissions and maintenance of the Trial Master File to ensure it remains audit-ready at all times.
- • Develop and sustain collaborative relationships with clinical investigators, institutions, internal stakeholders, and vendors to facilitate successful trial execution and operational efficiency.
- • Contribute to clinical study planning by participating in budget and contract negotiations, timeline forecasting, site identification and qualification, and process improvement initiatives within Global Clinical Affairs.
- • Prepare essential clinical study documents such as informed consent forms, clinical monitoring plans, and other trial-related templates to standardize operations across studies.
- • Work on multiple clinical trials simultaneously, prioritizing tasks and managing competing deadlines in a fast-paced, global environment.
- • Travel 20-70% within the United States, including overnight trips, with travel intensity potentially reaching 70% during peak study initiation phases.
- • Apply technical knowledge to understand and communicate about evolving diagnostic technologies and their clinical application in real-world settings.
- • Support retrospective and prospective biological sample procurement processes when required, ensuring proper handling and documentation of samples in alignment with study protocols.
- • Utilize electronic Trial Master Files (eTMF) and Clinical Trial Management Systems (CTMS) to maintain accurate, real-time records and streamline trial operations.
- • Demonstrate familiarity with point-of-care research environments and blood gas testing methodologies, particularly when supporting diagnostic trials in decentralized or mobile clinical settings.
- • Operate within Danaher’s Business System to drive continuous improvement, innovation, and scalable processes across global clinical operations.
- • Ensure all clinical activities align with Danaher’s mission to accelerate precision diagnostics and improve patient outcomes through faster, more accurate diagnostic results.
🎯 Requirements
- • Bachelor’s degree with 5+ years of clinical research experience OR Master’s degree with 3+ years of clinical research experience OR Doctoral degree in a relevant field with clinical research experience
- • Basic knowledge of regulatory requirements and Good Clinical Practice (GCP) for in vitro diagnostic (IVD) and medical device products
- • Proven experience managing clinical research sites and monitoring clinical trial data
- • Ability to work on multiple clinical projects simultaneously with strong organizational and time management skills
- • Willingness and ability to travel 20-70% within the United States, including overnight trips
🏖️ Benefits
- • Annual salary range of $103,000.00 - $130,000.00
- • Eligibility for bonus/incentive pay
- • Comprehensive benefits package including medical, dental, and vision insurance
- • 401(k) retirement plan
- • Paid time off
- • Remote work arrangement eligible within the United States
Skills & Technologies
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About Danaher Corporation
Danaher Corporation is a global science and technology innovator headquartered in Washington, D.C. Founded in 1969, it designs, manufactures, and markets medical, industrial, and commercial products and services to professional, medical, and scientific customers. Operating through three segments—Life Sciences, Diagnostics, and Environmental & Applied Solutions—Danaher owns brands such as Beckman Coulter, Cepheid, Leica Microsystems, and Hach. The company applies the Danaher Business System, a continuous-improvement methodology, to drive quality, delivery, cost, and innovation. With approximately 63,000 associates worldwide, Danaher focuses on accelerating diagnostics, advancing life-science research, and ensuring water quality and public health.
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