Clinical Research Coordinator: Lead Safe, Efficient Trials

Denali Health

Atlanta (GA)

On-site

USD 52,000 - 75,000

Full time

14 days+
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Job summary

Denali Health is seeking a highly organized Clinical Research Coordinator to support day-to-day study activities from start-up through closeout, ensuring trials are conducted safely and in accordance with protocol and regulatory requirements.

The role involves coordinating visits, screening, consent, data entry, regulatory documentation, and sponsor communication. A healthcare or life sciences degree is preferred, with prior clinical research experience a plus.

Qualifications

  • High school diploma or equivalent is listed as a baseline requirement.
  • Experience in clinical research and patient interactions is preferred.
  • Familiarity with study protocols, GCP, and regulatory requirements is advantageous.

Responsibilities

  • Coordinate assigned clinical research studies from site initiation through study closeout.
  • Review study protocols, informed consent forms, manuals, and schedules of assessments.
  • Prepare for and coordinate screening, enrollment, randomization, treatment, and follow-up visits.
  • Ensure all study procedures are completed within protocol-required timeframes.
  • Maintain accurate study calendars, visit schedules, and patient follow-up.

Skills

Attention to detail
Time management
Communication skills
Patient interaction
Regulatory compliance

Education

Associate's or Bachelor's degree in healthcare, life sciences, nursing, public health, or related field

Tools

EDC
CTMS
eSource
ePRO
IWRS/IRT

Job description

Denali Health is seeking a highly organized Clinical Research Coordinator to support day-to-day study activities from start-up through closeout, ensuring trials are conducted safely and in accordance with protocol and regulatory requirements.

The role involves coordinating visits, screening, consent, data entry, regulatory documentation, and sponsor communication. A healthcare or life sciences degree is preferred, with prior clinical research experience a plus.

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