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Sr Clinical Research Associate-Class III Device

Job in Minneapolis, Hennepin County, Minnesota, 55400, USA
Listing for: Kelly Services
Full Time, Part Time, Seasonal/Temporary position
Listed on 2026-08-28
Job specializations:
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 110000 USD Yearly USD 110000.00 YEAR
Job Description & How to Apply Below

Title:

Senior Clinical Research Associate-Medical Device Pay:
Starting at $110,000, DOE FT or PT:
Full-time, Contract-to-hire (about 3 months to conversion)

Location:

Remote with domestic travel (25-50% anticipated)

Kelly® Science & Clinical is seeking a Senior Clinical Research Associate for a temp-to-hire position at an early-stage, innovation-driven medical device client. If you're passionate about supporting high-impact clinical studies and improving patient care in surgical settings, and are ready to take the next step in your career, trust The Experts at Hiring Experts.

As a Senior Clinical Research Associate, you will be responsible for overseeing the execution of clinical trials from site start-up to site closure, ensuring compliance with study protocols, regulatory requirements, and maintaining quality documentation. Key responsibilities include coordinating and conducting site qualification, initiation, and monitoring visits; managing site operations; reviewing informed consent procedures; assessing investigational product accountability; and supporting the development of study documentation and site-facing presentation materials.

You will develop strong relationships with clinical site staff, proactively identify and mitigate risks, and facilitate timely communication among stakeholders.

Requirements
  • Bachelor's Degree or higher in healthcare or science related field (alternately, relevant experience may be considered)
  • Minimum 5 years' experience as a Clinical Research Associate
  • At least 3 years of monitoring Class III medical device trials
  • Proficiency with Epic required
  • Thorough knowledge of clinical research concepts, FDA regulations, and Good Clinical Practice (GCP)
  • Strong organizational, communication, and critical thinking skills
  • Willingness and ability to travel domestically 25-50% of the time
  • Experience in breast cancer, breast reconstruction, or related therapeutic areas preferred
  • Proficient in Microsoft Office and comfortable learning new clinical trial management systems

Our client offers a fast-paced, high-growth environment with opportunities for professional development and impactful work.

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Position Requirements
10+ Years work experience
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