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Closed listing

Clinical Research Operations Coordinator

  • Farmington Hills, MI, United States

From $35 USD / hour

This opening has closed.

The original listing is kept below for reference.

Job details

Pay
From $35 USD / hour
Experience
2+ years of experience in clinical research coordination, participant recruitment, patient scheduling, or clinical trial operations.
Posting language
English
Posted

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Original job description

Archived listing. The details below describe a past opening.

Required Skills & Experience

Qualifications

-2+ years of experience in clinical research coordination, participant recruitment, patient scheduling, or clinical trial operations. -Experience working directly with patients or research participants. -Strong organizational, communication, and coordination skills. -Familiarity with clinical research processes and participant-facing activities. -Bachelor's degree in a life science, healthcare, public health, psychology, or related field r

Job Description

Insight Global Health is hiring a Clinical Research Operations Coordinator to support participant recruitment, scheduling, and study operations for a clinical research initiate. This is onsite in Farmington Hills, MI 48331.

Schedule: Monday to Friday 8-6*hours may vary Duration: October - End of 2026

Additional Details:

Based primarily onsite at a clinic, this individual will serve as a key liaison between the research team and clinical site staff, ensuring a seamless participant experience and successful study execution. The role will focus primarily on participant recruitment, scheduling coordination, and operational support, while also gaining exposure to participant enrollment and moderated research sessions to build a comprehensive understanding of the study process.

Responsibilities

-Coordinate participant recruitment, screening, and enrollment activities. -Schedule participant visits, study sessions, and follow-up appointments. -Serve as the primary point of contact between the research team and clinical site staff. -Track recruitment progress and help maintain study timelines. -Communicate with participants and stakeholders to ensure smooth study operations. -Support participant enrollment and moderation sessions as needed to develop a strong understanding of the participant experience and study workflow. -Maintain accurate study records and documentation.

More about this job

Skills

  • Clinical research
  • Recruitment
  • Scheduling
  • Research
  • Communication skills
  • Workflow

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