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    • Familiarity with medical terminology relevant to clinical research settings.
    • Experience in clinical research or a related area is highly desirable.
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    • This role requires a strong understanding of medical terminology and the ability to work effectively in a fast-paced clinical environment.
    • Proficient understanding of medical terminology related to cardiology and ECG procedures.
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    • Strong understanding of medical terminology and healthcare procedures.
    • Background in research or clinical studies is a plus.
    • Send messages to physicians or nurses as appropriate, for clinical-related questions or concerns relayed by patients’.
    • Patient Reception and Check-In:.
    • Sound knowledge of clinical trial conduct preferably with front-line experience as a clinical trials coordinator.
    • Performs online clinical literature searches and complies with copyright requirements.
    • Completes a variety of documents that may include clinical study…
    • Knowledge of medical terminology, privacy requirements, and primary care workflows.
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    • Knowledge of medical terminology and clinic workflow procedures.
    • 1-3 years of experience in medical administration or clinical reception.
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    • Support architectural consistency across integrations involving clinical…
    • Receive, scan and document all pertinent clinical information in compliance with SOP/protocol and applicable legislation.
    • Bilingual, English/French is required.
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clinical coordinator

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Clinical Research Coordinator
A3-4-8279 Lundy's Lane, Niagara Falls, ON
$23–$30 an hour
Full-time

Job details

$23–$30 an hour
On-site parking
Full-time
A3-4-8279 Lundy's Lane, Niagara Falls, ON

Full job description

Overview
The Clinical Research Coordinator plays a vital role in the planning, implementation, and management of clinical trials. This position requires a detail-oriented individual who can effectively oversee research protocols and ensure compliance with regulatory standards. The ideal candidate will possess strong organizational skills, a solid understanding of medical terminology, and the ability to work collaboratively with various stakeholders including researchers, healthcare professionals, and study participants.

Duties

  • Coordinate and manage all aspects of clinical trials from initiation to completion.
  • Collect and manage data accurately, ensuring adherence to study protocols.
  • Conduct patient assessments and oversee the recruitment process for study participants.
  • Perform phlebotomy as required for sample collection.
  • Supervise research staff and provide training on study procedures.
  • Analyze data collected during trials to ensure integrity and accuracy.
  • Maintain comprehensive documentation of trial activities, including regulatory submissions and reports.
  • Communicate effectively with investigators, sponsors, and regulatory bodies regarding trial progress.

Qualifications

  • Bachelor’s degree in a related field such as nursing or life sciences is preferred.
  • Experience in clinical research or a related area is highly desirable.
  • Proficiency in data management and analysis techniques.
  • Familiarity with medical terminology relevant to clinical research settings.
  • Strong supervisory skills with experience leading teams or coordinating projects.
  • Excellent organizational skills with the ability to manage multiple tasks simultaneously.
  • Effective communication skills, both written and verbal, to interact with diverse groups.

This position is essential for advancing clinical knowledge and improving patient care through rigorous research practices. If you are passionate about contributing to the field of clinical research and possess the necessary qualifications, we encourage you to apply.

Job Type: Full-time

Pay: $23.00-$30.00 per hour

Expected hours: 37.5 – 44 per week

Benefits:

  • On-site parking

Work Location: In person

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