Clinical Research Coordinator II

Baltimore, MD, US β€’ Posted 12 hours ago β€’ Updated 12 hours ago
Contract W2
On-site
Depends on Experience
Fitment

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Job Details

Skills

  • Clinical Research
  • Collaboration
  • Nursing
  • Clinical Trials

Summary

We are seeking a Clinical Research Coordinator II to support ongoing clinical studies and ensure compliance with FDA, Google Cloud Platform, and ICH guidelines. The coordinator will manage patient recruitment, study visits, documentation, and data entry while ensuring patient safety and protocol compliance.

Key Responsibilities:

  • Coordinate and conduct clinical research activities according to study protocols

  • Recruit, enroll, and retain study participants

  • Obtain informed consent and perform protocol procedures (vital signs, ECG, height, weight, pregnancy tests, etc.)

  • Schedule and manage subject visits within protocol timelines

  • Maintain source documents, patient records, and study files

  • Enter and manage study data in EDC/CRF systems and resolve queries

  • Ensure IRB approvals and compliance with regulatory guidelines

  • Participate in site initiation and study training meetings

Required Qualifications:

  • Bachelor s degree in a clinical/medical field

  • Active Nursing License (RN / LVN / LPN)

  • 2+ years of clinical research or clinical trial coordination experience

  • Knowledge of Google Cloud Platform, FDA, ICH, and IRB processes

  • Strong communication, documentation, and organizational skills

  • Basic computer and data entry skills

Employers have access to artificial intelligence language tools (β€œAI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: 80168598
  • Position Id: 8910060
  • Posted 12 hours ago
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