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Clinical Research Coordinator I

Job

Insight Global, LLC

Newton, KS (In Person)

Full-Time

Posted 1 day ago (Updated 1 hour ago) • Actively hiring

Expires 6/15/2026

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Job Description

Job Description The Clinical Research Coordinator I supports and manages day-to-day activities for clinical research studies, ensuring strict compliance with FDA regulations, GCP guidelines, sponsor protocols, and IRB requirements. This role partners closely with investigators, sponsors, CROs, and participants to ensure accurate execution, documentation, and successful study completion. Key Responsibilities
FDA GCP IRB SAE ALCOA
We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.

To learn more about how we collect, keep, and process your private information, please review
Insight Global's Workforce Privacy Policy:
https://insightglobal.com/workforce-privacy-policy/. Skills and Requirements
  • 1+ year of clinical research experience
  • Formal medical training, healthcare education, or hands-on clinical experience
  • Strong knowledge of medical terminology
  • Ability to perform clinical and diagnostic procedures (vitals, labs, etc.)
  • Experience with AE/ SAE reporting and informed consent preferred
  • Strong organizational, multitasking, and time-management skills
  • Excellent written, verbal, and interpersonal communication skills
  • Proficient with office software and site documentation systems
  • Ability to work independently in a fast-paced research environment
  • Ability to be ambulatory most of the day and lift/manipulate equipment as needed
  • Experience as an LPN To view full details and how to apply, please login or create a Job Seeker account

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