Phlebotomist and Program Coordinator

Phlebotomist and Program Coordinator

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work saves livesand 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.

As a global leader in clinical diagnostics, Beckman Coulter Diagnostics has challenged convention to elevate the diagnostic laboratory's role in improving patient health for more than 90 years. Our diagnostic solutions are used in routine and complex clinical testing, and are used in hospitals, reference and research laboratories, and physician offices around the world. Every hour around the world, more than one million tests are run on Beckman Coulter Diagnostics systems, impacting 1.2 billion patients and more than three million clinicians per year. From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to more rigorous decision makingwe are enabling clinicians to deliver the best possible care to their patients with improved efficiency, clinical confidence, adaptive collaboration, and accelerated intelligence.

Learn about the Danaher Business System which makes everything possible.

The Phlebotomist and Program Coordinator is responsible for daily internal blood draw activities and coordinating on-site donors to support daily production operations in Chaska, MN. This role serves as the primary point of contact for study execution, including participant recruitment, scheduling, study enrollment, and informed consent, while ensuring compliance with Good Clinical Practice (GCP), protocol requirements, participant safety, and data integrity. This role will also support other production operations as needed. This position reports to Manager Operations and requires direct interaction and collaboration with cross-functional team members.

This position reports to the Manager Operations and is part of the Hardware Operations Team located in Chaska, MN and will be an on-site role.

In this role, you will have the opportunity to:

• Lead the day-to-day operations of the Internal Blood Draw Program, coordinating participant scheduling, supporting study enrollment and informed consent activities, and ensuring compliance with IRB-approved protocols, Good Clinical Practice (GCP), and HIPAA requirements.
• Perform intravenous blood collection procedures while maintaining the highest standards of participant safety, protocol adherence, data integrity, and quality while being a part of the medical device industry.
• Support operational excellence through inventory and equipment management, cross-functional collaboration with EHS and clinical teams, and participation in training and study-related activities that enable successful program execution.

The essential requirements of the job include:

• 2-year associates degree or higher degree required, with credentials demonstrating proficiency and education in phlebotomy
• Required a minimum of 3+ years of experience performing intravenous blood draws.
• Demonstrated ability to maintain strict infection control practices, safety standards, and universal precautions in clinical, medical, and laboratory environments while effectively interacting with participants, explaining technical information, assessing donor eligibility, and ensuring accurate, real-time documentation and data entry.

Travel, Motor Vehicle Record & Physical/Environment Requirements:

• Ability to lift, move or carry equipment up to 30lbs.
• Ability to stand and work on your feet daily.
• This position demands a high degree of autonomy, with responsibility for individual task management.

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

• Preferred background in a medical, laboratory, or clinical research field, such as Medical Laboratory Technology or Clinical Laboratory Science, or certification in phlebotomy.
• Experience working in a regulated manufacturing environment with knowledge of Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), quality compliance requirements, and the ability to read, interpret, and follow Standard Operating Procedures (SOPs).
• Proficient in Windows-based systems and Microsoft Office applications, including Outlook, Word, Excel, PowerPoint, and Teams, with strong documentation and organizational skills.

Beckman Coulter Diagnostics, 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.

The annual hourly range for this role is $32-$38. 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 Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law.

Join our winning team today. Together, we'll 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.

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.