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Clinical Research Coordinator

Ki Health Partners
Posted 20 hours ago, valid for 17 days
Location

Monroe, CT, US

Salary

$45,000 - $55,000 per year

Contract type

Full Time

Health Insurance
Paid Time Off
Employee Discounts

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Sonic Summary

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  • Ki Health Partners is seeking a Clinical Research Coordinator in New Haven, CT, offering a competitive salary and benefits including health insurance and 401(k) matching.
  • The ideal candidate should have a Bachelor's degree in life sciences or a related field and 1-3 years of experience in clinical research coordination.
  • Key responsibilities include managing clinical trial operations, enrolling study participants, and maintaining accurate study data using electronic data capture systems.
  • Candidates should be familiar with FDA regulations and ICH-GCP guidelines, with strong organizational skills and excellent communication abilities.
  • Ki Health Partners promotes a collaborative culture and offers opportunities for advancement within a mission-driven healthcare organization.
Benefits:
  • 401(k)
  • Employee discounts
  • Health insurance
  • Paid time off
  • 401(k) matching
  • Dental insurance
  • Opportunity for advancement
  • Profit sharing
  • Vision insurance
About the Role:
Ki Health Partners is looking for a passionate and detail-oriented Clinical Research Coordinator to join their growing team in New Haven, CT. This is an exciting opportunity to play a meaningful role in advancing clinical research and improving patient outcomes. If you thrive in a fast-paced, science-driven environment, we want to hear from you!

Responsibilities:
  • Coordinate and manage day-to-day clinical trial operations in compliance with GCP and regulatory guidelines
  • Screen, enroll, and follow up with study participants throughout the duration of clinical studies
  • Collect, record, and maintain accurate study data using electronic data capture (EDC) systems
  • Serve as a primary point of contact for study sponsors, IRBs, and research staff
  • Prepare and submit regulatory documents, including IRB submissions, amendments, and continuing reviews
  • Monitor patient safety and report adverse events in accordance with protocol requirements
  • Support site initiation visits, monitoring visits, and audits conducted by sponsors or regulatory agencies
Requirements:
  • Bachelor's degree in life sciences, healthcare, or a related field
  • 1–3 years of experience in clinical research coordination or a similar role
  • Familiarity with FDA regulations, ICH-GCP guidelines, and IRB processes
  • Proficiency with EDC systems and clinical trial management software (CTMS)
  • SOCRA or ACRP certification (CCRP or CCRC) preferred
  • Strong organizational skills with exceptional attention to detail
  • Excellent interpersonal and communication skills for working with patients and multidisciplinary teams
About Us:
Ki Health Partners is a forward-thinking healthcare organization dedicated to driving innovation in clinical research and patient care. Our team is committed to fostering a collaborative, mission-driven culture where every employee's contributions make a real difference. At Ki Health Partners, you'll find a supportive environment that values professional growth, scientific excellence, and meaningful impact.



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