Senior Clinical Research Associate - Remote

Beckman Coulter Diagnostics

Round Rock Texas

United States

Scientific Research
(No Timezone Provided)

Wondering what’s within Beckman Coulter?

Take a closer look.

Join a team where you can be heard, be supported, and always be yourself. At Beckman Coulter, a Danaher company, we’re building a culture that celebrates backgrounds, experiences, and perspectives of all our associates. We are dedicated to advancing and optimizing the laboratory to move science and health care forward for more than 80 years. Find the opportunity to build relevant career, be creative, and try new things with the support needed to be successful. Find the , which makes everything possible.

Witness our shared purpose—helping realize life’s potential—in action.

What you find at Beckman Coulter —and within yourself — might just change the world!

The Sr. Clinical Research Associate for Beckman Coulter Diagnostics is responsible providing expert and overall support to clinical study teams and for all key phases of the assigned clinical studies, including planning, execution, analysis, reports & close-out.

This position is part of the Beckman Coulter Chemistry & Immunoassay business and will be located in Chaska, MN (or remotely). At Beckman we take great research and generate the evidence to create an easy to use and reliable product.

This position is on the Clinical Affairs Team and report to the Sr. Manager of Clinical Operations responsible for planning and execution of a portfolio of both pre-market and post-market clinical research programs for the Chemistry & Immunoassay business.

In this role, you will have the opportunity to:

  • Participate in the key phases of the external clinical study, including planning, execution, analysis & close-out. This includes drafting the necessary documents for each phase.
  • Support final study site selection, contract process and site initiation visits; participates in investigators meetings and other training of site personnel on the clinical study protocol, database, and investigator responsibilities.
  • Execute the clinical study monitoring plan, with interim and risk-based monitoring visits to verify site compliance to the study protocol and applicable regulations.
  • Review data and support database development and maintenance with selected database vendor representatives.
  • Supports final study site selection, contract process and site initiation visits; participates in investigators meetings and other training of site personnel on the clinical study protocol, database, and investigator responsibilities.
  • The essential requirements of the job include:

  • Bachelor’s degree with 3-5 years’ experience related to in vitro diagnostics, advanced degree a plus.
  • Experience with clinical study management and monitoring for clinical diagnostics, medical devices or pharmaceutical products in a regulated environment.
  • Functional knowledge of Good Clinical Practice, certification a plus, and familiar with US and OUS requirements for design control and clinical study management.
  • Experience working with data management tools and understanding of databases and general statistical concepts.
  • Willing and able to develop appropriate internal or external technical expertise required and coordinate efforts to resolve technical issues that may arise during clinical trials.
  • Able to travel up to 30% of the time, depending on business needs.
  • It would be a plus if you also possess previous experience in:

  • Clinical research certification (such as CCRA, CCRC)
  • Beckman Coulter, a Danaher company, offers a broad array of comprehensive, competitive benefit programs that add value to associates. Whether it’s a health care program or paid time off, our programs add to life beyond the job. Check out our benefits at . We believe you’ll like what you see!

    At Beckman Coulter, we’re driven by a sense of wonder for what we can create—and what we can become. Here, you’ll accelerate your career while driving innovation that improves lives. You’ll work hard and try new things, with guidance from committed leaders, powerful DBS tools, and the support of a global organization. As part of the Danaher's 67,000 associates across the globe, your possibilities for growth and development are unparalleled.

    We believe that creativity and innovation thrive when the most diverse set of voices are heard, and that’s why we’re taking concrete steps to ensure that we’re fostering an engaging workplace. If you’d like to learn more, read stories from our associates on our or contact one of our recruiters.

    Senior Clinical Research Associate - Remote

    Beckman Coulter Diagnostics

    Round Rock Texas

    United States

    Scientific Research

    (No Timezone Provided)

    Wondering what’s within Beckman Coulter?

    Take a closer look.

    Join a team where you can be heard, be supported, and always be yourself. At Beckman Coulter, a Danaher company, we’re building a culture that celebrates backgrounds, experiences, and perspectives of all our associates. We are dedicated to advancing and optimizing the laboratory to move science and health care forward for more than 80 years. Find the opportunity to build relevant career, be creative, and try new things with the support needed to be successful. Find the , which makes everything possible.

    Witness our shared purpose—helping realize life’s potential—in action.

    What you find at Beckman Coulter —and within yourself — might just change the world!

    The Sr. Clinical Research Associate for Beckman Coulter Diagnostics is responsible providing expert and overall support to clinical study teams and for all key phases of the assigned clinical studies, including planning, execution, analysis, reports & close-out.

    This position is part of the Beckman Coulter Chemistry & Immunoassay business and will be located in Chaska, MN (or remotely). At Beckman we take great research and generate the evidence to create an easy to use and reliable product.

    This position is on the Clinical Affairs Team and report to the Sr. Manager of Clinical Operations responsible for planning and execution of a portfolio of both pre-market and post-market clinical research programs for the Chemistry & Immunoassay business.

    In this role, you will have the opportunity to:

  • Participate in the key phases of the external clinical study, including planning, execution, analysis & close-out. This includes drafting the necessary documents for each phase.
  • Support final study site selection, contract process and site initiation visits; participates in investigators meetings and other training of site personnel on the clinical study protocol, database, and investigator responsibilities.
  • Execute the clinical study monitoring plan, with interim and risk-based monitoring visits to verify site compliance to the study protocol and applicable regulations.
  • Review data and support database development and maintenance with selected database vendor representatives.
  • Supports final study site selection, contract process and site initiation visits; participates in investigators meetings and other training of site personnel on the clinical study protocol, database, and investigator responsibilities.
  • The essential requirements of the job include:

  • Bachelor’s degree with 3-5 years’ experience related to in vitro diagnostics, advanced degree a plus.
  • Experience with clinical study management and monitoring for clinical diagnostics, medical devices or pharmaceutical products in a regulated environment.
  • Functional knowledge of Good Clinical Practice, certification a plus, and familiar with US and OUS requirements for design control and clinical study management.
  • Experience working with data management tools and understanding of databases and general statistical concepts.
  • Willing and able to develop appropriate internal or external technical expertise required and coordinate efforts to resolve technical issues that may arise during clinical trials.
  • Able to travel up to 30% of the time, depending on business needs.
  • It would be a plus if you also possess previous experience in:

  • Clinical research certification (such as CCRA, CCRC)
  • Beckman Coulter, a Danaher company, offers a broad array of comprehensive, competitive benefit programs that add value to associates. Whether it’s a health care program or paid time off, our programs add to life beyond the job. Check out our benefits at . We believe you’ll like what you see!

    At Beckman Coulter, we’re driven by a sense of wonder for what we can create—and what we can become. Here, you’ll accelerate your career while driving innovation that improves lives. You’ll work hard and try new things, with guidance from committed leaders, powerful DBS tools, and the support of a global organization. As part of the Danaher's 67,000 associates across the globe, your possibilities for growth and development are unparalleled.

    We believe that creativity and innovation thrive when the most diverse set of voices are heard, and that’s why we’re taking concrete steps to ensure that we’re fostering an engaging workplace. If you’d like to learn more, read stories from our associates on our or contact one of our recruiters.