Beckman Coulter

Senior Clinical Research Associate (onsite)

Beckman Coulter

Chaska, MN 55318, USA
Full-TimeDepends on ExperienceSenior LevelMasters
Job Description

Are you an experienced Clinical Research Associate looking to take the next step in your career? Beckman Coulter is seeking a highly motivated and skilled Senior Clinical Research Associate to join our team onsite. In this role, you will have the opportunity to work on cutting-edge clinical research projects and contribute to the development of life-saving medical technology. Our ideal candidate is a driven and detail-oriented individual with a strong background in clinical research and a passion for making a difference in the lives of patients. If you are ready to take on a new and exciting challenge, we encourage you to apply for this position and join our dynamic and innovative team at Beckman Coulter.

  1. Conduct clinical research projects: The Senior Clinical Research Associate will be responsible for planning, organizing, and executing clinical research projects in accordance with company and industry standards.
  2. Ensure compliance: The Senior Clinical Research Associate will ensure all clinical research activities are in compliance with FDA regulations, Good Clinical Practice (GCP), and company policies.
  3. Monitor and track progress: The Senior Clinical Research Associate will monitor and track the progress of clinical research projects, and report any issues or delays to the project manager.
  4. Train and mentor junior staff: The Senior Clinical Research Associate will provide training and mentorship to junior staff, and assist in their development and growth within the company.
  5. Manage study sites: The Senior Clinical Research Associate will manage study sites and maintain strong relationships with investigators and site staff to ensure timely and accurate completion of research activities.
  6. Review and analyze data: The Senior Clinical Research Associate will review and analyze clinical data, and identify any trends or issues that may impact the study results.
  7. Prepare study documentation: The Senior Clinical Research Associate will be responsible for preparing and maintaining all study documentation, including study protocols, informed consent forms, and case report forms.
  8. Collaborate with cross-functional teams: The Senior Clinical Research Associate will work closely with cross-functional teams, including clinical operations, regulatory affairs, and medical affairs, to ensure the successful execution of clinical research projects.
  9. Identify and mitigate risks: The Senior Clinical Research Associate will proactively identify and mitigate potential risks and issues during the course of the study.
  10. Participate in meetings and conferences: The Senior Clinical Research Associate will represent the company at meetings and conferences, and present study updates and results to internal and external stakeholders.
  11. Stay current with industry developments: The Senior Clinical Research Associate will stay up-to-date with industry developments and trends, and apply this knowledge to improve study processes and procedures.
  12. Adhere to ethical standards: The Senior Clinical Research Associate will adhere to ethical standards and maintain patient
Where is this job?
This job is located at Chaska, MN 55318, USA
Job Qualifications
  • Bachelor's Or Master's Degree In A Scientific Or Healthcare Related Field

  • Minimum Of 5 Years Experience As A Clinical Research Associate, Preferably In The Medical Device Industry

  • Strong Knowledge Of Clinical Research Methodology And Regulations, Including Good Clinical Practice (Gcp) And International Conference On Harmonisation (Ich) Guidelines

  • Excellent Communication And Interpersonal Skills, With The Ability To Effectively Interact With Cross-Functional Teams, Study Site Staff, And External Stakeholders

  • Experience With Managing And Monitoring Clinical Trials, Including Site Initiation, Site Monitoring, Data Collection And Review, And Study Close-Out Activities

Required Skills
  • Quality Control

  • Data collection

  • Site management

  • FDA regulations

  • Patient Recruitment

  • Informed Consent

  • Protocol Management

  • Site Monitoring

  • Adverse Event Reporting

  • Study Documentation

  • Investigator Training

Soft Skills
  • Communication

  • Emotional Intelligence

  • Leadership

  • Time management

  • Interpersonal Skills

  • creativity

  • Organization

  • Teamwork

  • Adaptability

  • Problem-Solving

Compensation

According to JobzMall, the average salary range for a Senior Clinical Research Associate (onsite) in Chaska, MN 55318, USA is $83,252 - $102,182 per year. This range may vary depending on factors such as experience, education, and specific job responsibilities. Additionally, benefits and bonuses may also impact the overall salary for this position.

Additional Information
Beckman Coulter is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
Required LanguagesEnglish
Job PostedJanuary 10th, 2025
Apply BeforeApril 11th, 2026
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About Beckman Coulter

Beckman Coulter Inc., is a Danaher Corporation company that develops, manufactures and markets products that simplify, automate and innovate complex biomedical testing.

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