Clinical Research Coordinator: Drive Trial Excellence & Patient Care

Ki Health Partners

New Haven (CT)

On-site

USD 52,000 - 70,000

Full time

14 days+
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Benefits offered by this job

401(k)
Employee discounts
Health insurance
Paid time off
401(k) matching
Dental insurance
Opportunity for advancement
Profit sharing
Vision insurance

Job summary

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! The role involves coordinating day-to-day trial operations, screening and enrolling participants, managing data with EDC/CTMS, and serving as a primary

Qualifications

  • Bachelor's degree in life sciences, healthcare, or related field.
  • 1–3 years of experience in clinical research coordination or similar role.
  • Familiarity with FDA regulations, ICH-GCP, and IRB processes.
  • Proficiency with EDC systems and CTMS.
  • SOCRA or ACRP certification preferred (CCRP or CCRC).
  • Strong organizational skills with exceptional attention to detail.
  • Excellent interpersonal and communication skills for working with patients and multidisciplinary teams.

Responsibilities

  • Coordinate and manage day-to-day clinical trial operations per 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.

Skills

Organizational skills
Communication skills
Attention to detail

Education

Bachelor's degree in life sciences
SOCRA or ACRP certification preferred (CCRP/CCRC)

Tools

EDC systems
CTMS

Job description

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! The role involves coordinating day-to-day trial operations, screening and enrolling participants, managing data with EDC/CTMS, and serving as a primary

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