Clinical Research Coordinator

3 weeks ago

Columbia, United States Advanced Recruiting Partners Full time

Overview: As a Clinical Research Coordinator I, you will play a pivotal role in the execution of clinical trials, ensuring adherence to protocol requirements, ethical standards, and regulatory guidelines. You will be responsible for patient recruitment, study coordination, data management, communication, adverse event reporting, and maintaining on-site presence.

Responsibilities:

  1. Patient Recruitment:

    • Actively recruit and enroll eligible patients into clinical trials.
    • Ensure adherence to protocol requirements and ethical standards during patient recruitment processes.

  2. Study Coordination:

    • Coordinate all aspects of clinical trial activities.
    • Schedule patient visits, obtain informed consent, and manage study documentation.
    • Coordinate and oversee onsite monitoring visits to ensure compliance with protocol requirements.

  3. Data Management:

    • Maintain Electronic Data Capture (EDC) systems.
    • Ensure accurate and timely entry of study data.
    • Ensure compliance with regulatory guidelines regarding data management.

  4. Communication:

    • Serve as a liaison between study participants, healthcare professionals, and study sponsors.
    • Provide clear and compassionate communication throughout the research process.
    • Address any concerns or questions from study participants or stakeholders.

  5. Adverse Event Reporting:

    • Promptly report and document adverse events according to established procedures.
    • Ensure patient safety by adhering to adverse event reporting guidelines.

  6. On-Site Presence:

    • Be available and attend clinical cases and planned study visits.
    • Assist in gaining informed consent, performing assessments, and ensuring protocol compliance.
    • Particularly maintain on-site presence in the Columbia, South Carolina area.

Qualifications:

  • Bachelor's degree in a relevant field (e.g., biology, nursing, healthcare).
  • Previous experience in clinical research coordination or a related field preferred.
  • Familiarity with regulatory requirements and Good Clinical Practice (GCP) guidelines.
  • Strong organizational and communication skills.
  • Ability to work effectively in a team environment and independently.
  • Attention to detail and ability to manage multiple tasks simultaneously.
  • Flexibility to adapt to changing priorities and work schedules.
  • Proficiency in Microsoft Office Suite and Electronic Data Capture (EDC) systems.
#IND

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