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Senior Clinical Research Associate

Job in Austin, Travis County, Texas, 78716, USA
Listing for: Kelly Science, Engineering, Technology & Telecom
Full Time position
Listed on 2026-07-08
Job specializations:
  • Healthcare
    Clinical Research, Medical Science
Job Description & How to Apply Below

Kelly Science and Clinical FSP is currently seeking a Regional Clinical Research Associate for a long-term engagement in the US with one of our Global Medical Device clients. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full-time and is offering full benefit options. As a Kelly FSP employee you will be eligible for Medical, Dental, Vision, 401K and a variety of other benefits to choose from.

You will also be eligible for paid time off, including holiday, vacation, and sick/personal time.

Senior Clinical Research Associate

Travel up to 75%

  • To support 1-3 protocols in the cardiovascular/electrophysiology medical device space.
  • The ideal candidate will have cardiovascular medical device monitoring experience- however, cardiovascular/electrophysiology pharma monitoring experience will be considered.
  • 5 years of monitoring experience required.
  • Bachelor’s degree is required, preferably a Bachelor of Science Degree in Life Science, Physical Science, Nursing or Biological Science.
  • Candidates must have in-depth knowledge of FDA regulations and ICH/GCP guidelines.
  • Strong problem-solving skills to mitigate risks and identify issues at sites and implement effective solutions promptly.
  • Strong interpersonal skills to establish and maintain effective working relationships with site personnel, investigators, and internal teams.
  • Exceptional verbal and written communication skills, with the ability to convey complex information clearly and concisely.
  • Ability to tailor communication style to the needs and preferences of different stakeholders, fostering a collaborative environment.
  • Ability to work independently and manage multiple priorities in a dynamic environment.
  • A well-executed plan for communication with the study teams and sites.
  • Well-versed in clinical trial management. They are rigorous, detail-oriented, and precise in their report.
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Position Requirements
10+ Years work experience
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