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Clinical Research Coordinator

2 weeks ago

Stoney Creek, Ontario, Canada ClinSurge Research Full time

Job Overview

We are seeking a dedicated and detail-oriented Clinical Research Coordinator to join our team. This role involves managing and overseeing clinical research studies, ensuring compliance with protocols, and maintaining accurate data collection. The ideal candidate will have a strong background in research, data management, and medical terminology, with experience in supervising clinical activities. This position offers an opportunity to contribute to impactful medical research in a collaborative environment focused on advancing healthcare.

Responsibilities

  • Coordinate and oversee clinical research studies from initiation to completion, ensuring adherence to study protocols and regulatory requirements.
  • Recruit, screen, and enroll study participants, including performing phlebotomy when necessary.
  • Collect, record, and manage data accurately using electronic data capture systems.
  • Maintain detailed documentation of study activities, adverse events, and protocol deviations.
  • Communicate effectively with study participants, healthcare providers, and regulatory bodies.
  • Ability to do phlebotomy, process and ship according to protocol and IATA regulations.
  • Ensure compliance with all ethical standards, safety protocols, and confidentiality requirements.
  • Assist in analyzing collected data to support research findings and prepare reports or publications as needed.

Qualifications

  • Proven experience in research coordination or a related healthcare setting.
  • Strong knowledge of data management systems and data collection techniques.
  • Proficiency in medical terminology and basic analysis skills for interpreting research data.
  • Experience with phlebotomy and clinical procedures is highly desirable.
  • Supervising experience in a clinical or research environment is preferred.
  • Background in nursing or healthcare-related fields is advantageous.
  • Excellent organizational skills with attention to detail to ensure accuracy in data recording and compliance documentation.
  • Ability to work independently as well as part of a multidisciplinary team in a fast-paced environment. This position is integral to advancing clinical research efforts and improving patient outcomes through meticulous study management and data integrity.

Job Type: Full-time

Pay: $55,000.00-$65,000.00 per year

Benefits:

  • Dental care
  • Extended health care
  • On-site parking
  • Paid time off
  • Vision care

Work Location: In person