Masimo

Clinical Research Associate

Masimo

Irvine, CA, USA
Full-TimeDepends on ExperienceSenior LevelMasters
Job Description

Are you passionate about making a difference in the world of healthcare? Do you have experience in clinical research and a strong attention to detail? Masimo is seeking a highly motivated and dedicated Clinical Research Associate to join our team. As a global leader in non-invasive patient monitoring technologies, Masimo is committed to improving patient outcomes and reducing healthcare costs. In this role, you will have the opportunity to support and contribute to our cutting-edge research projects and clinical trials. If you are looking for a challenging and rewarding career in a fast-paced and innovative environment, then we want to hear from you!

  1. Conduct and oversee various clinical research projects and trials in accordance with company protocols and regulations.
  2. Collaborate with cross-functional teams to ensure the successful planning, execution, and completion of clinical studies.
  3. Collect, analyze, and maintain accurate and detailed records of all study data.
  4. Monitor and track study progress, identifying and addressing any issues or concerns that may arise.
  5. Ensure all study documentation and reports are completed accurately and in a timely manner.
  6. Develop and maintain relationships with study investigators and site staff.
  7. Conduct site visits and train site staff on study protocols and procedures.
  8. Organize and coordinate study supplies and equipment.
  9. Participate in the development and implementation of study protocols and procedures.
  10. Keep abreast of industry trends and regulations to ensure compliance with all applicable guidelines.
  11. Communicate regularly with study team members to provide updates and troubleshoot any issues.
  12. Ensure the safety and well-being of study participants at all times.
  13. Contribute to the development and improvement of company research processes and procedures.
  14. Attend and present at relevant conferences and meetings to share study findings and contribute to the advancement of medical knowledge.
  15. Maintain confidentiality of all study-related information.
  16. Adhere to ethical standards and guidelines in all aspects of research.
  17. Foster a positive and collaborative work environment within the research team.
  18. Continuously seek ways to improve and enhance the quality and efficiency of research activities.
  19. Represent the company in a professional and ethical manner at all times.
  20. Demonstrate a strong commitment to the company's mission and values.
Where is this job?
This job is located at Irvine, CA, USA
Job Qualifications
  • Bachelor's Or Master's Degree In A Relevant Field Such As Life Sciences, Pharmacy, Or Nursing.

  • Minimum Of 2-3 Years Of Experience In Clinical Research, Preferably In A Medical Device Or Pharmaceutical Company.

  • Excellent Understanding Of Good Clinical Practice (Gcp) Guidelines And Regulatory Requirements.

  • Strong Communication And Interpersonal Skills To Effectively Collaborate With Cross-Functional Teams And External Stakeholders.

  • Ability To Manage Multiple Projects, Prioritize Tasks, And Meet Deadlines In A Fast-Paced And Dynamic Environment.

Required Skills
  • Quality Assurance

  • Data Analysis

  • Regulatory compliance

  • Site management

  • Good Clinical Practice

  • Informed Consent

  • Protocol Management

  • Adverse Event Reporting

  • Study Monitoring

  • Subject Recruitment

  • Investigator Training

Soft Skills
  • Communication

  • Conflict Resolution

  • Leadership

  • Time management

  • creativity

  • Attention to detail

  • Teamwork

  • Adaptability

  • Problem-Solving

  • Empathy

Compensation

According to JobzMall, the average salary range for a Clinical Research Associate in Irvine, CA, USA is $68,000 to $102,000 per year. This can vary depending on the specific company, experience level, and education of the individual. Some Clinical Research Associates may also receive bonuses or other forms of compensation in addition to their base salary.

Additional Information
Masimo 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 PostedJuly 17th, 2024
Apply BeforeJune 21st, 2025
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About Masimo

Masimo is an American Irvine, California-based manufacturer of noninvasive patient monitoring technologies. The company sells more pulse oximetry to hospitals than any other company.

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