Clinical Research Coordinator - Patient-Centered Trials

Primary Clinical Research

Omaha (NE)

On-site

USD 52,000 - 76,000

Full time

14 days+
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Job summary

Primary Clinical Research in Omaha seeks a Clinical Research Coordinator to manage all aspects of assigned trials on-site. You will screen participants, recruit, schedule visits, and obtain informed consent in compliance with study protocols.

Daily tasks include collecting data, maintaining source documents, updating databases, and coordinating with investigators, sponsors, and CROs. Strong knowledge of GCP/ICH and regulatory standards is essential.

Qualifications

  • Strong knowledge of clinical research operations and good clinical practice.
  • Experience handling informed consent procedures and regulatory requirements.
  • Familiarity with study protocol requirements and data documentation.
  • Proficiency with data capture and source documentation.
  • Excellent organizational and communication skills.

Responsibilities

  • Coordinate all aspects of assigned clinical trials.
  • Screen participants, recruit, and schedule visits.
  • Obtain informed consent and ensure protocol adherence.
  • Collect and document study data, maintain source documents.
  • Update electronic databases and collaborate with investigators, sponsors and CROs.
  • Monitor participant safety and support audits/monitoring visits.

Skills

Clinical research operations
Informed consent
Study protocol knowledge
GCP/ICH compliance
Organizational skills
Communication skills
EDC systems

Education

Bachelor's degree in health-related or scientific field

Job description

Primary Clinical Research in Omaha seeks a Clinical Research Coordinator to manage all aspects of assigned trials on-site. You will screen participants, recruit, schedule visits, and obtain informed consent in compliance with study protocols.

Daily tasks include collecting data, maintaining source documents, updating databases, and coordinating with investigators, sponsors, and CROs. Strong knowledge of GCP/ICH and regulatory standards is essential.

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