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    • Up to 1 year clinical research experience preferred; experience in recruiting patients for research studies or clinical trials.
    • Knowledge of ICH/GCP guidelines.
    • Previous experience working on vaccine clinical trials.
    • Previous experience in an unblinded clinical trial role.
    • Exceptional attention to detail and accuracy.
    • Experience in clinical research is an asset.
    • Previous clinical research experience is considered an asset.
    • Clinical research: 1 year (preferred).
    • Demonstrated leadership, clinical and administrative skills.
    • Provide clinical and administrative supervision for a team(s) of registered Counsellors.
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    • This role requires a minimum of 40% on-site presence.
    • Additional on-site work may be required based on business needs.
    • Employment status: Regular full-time.
    • 3 year clinical experience (Required).
    • We offer a competitive compensation package that rewards experience and clinical excellence.
    • Consistently meet or exceed all quality and clinical indicators for residents, in alignment with organizational and legislative guidelines, through the…
    • Support account growth and partnership expansion by identifying opportunities for extensions, hybrid clinical–RWLP approaches, repeat work, and preferred…
    • O Serve as a role model of professionalism and ethics in nursing practice.
    • O Supervise students in clinical settings, ensuring adherence to safety protocols,…
    • Medical Degree and a minimum of three (3) years of clinical experience.
    • At the direction of the Clinical Director, the Associate Clinical Director may be asked…
    • A great awareness of and commitment to professional ethics.
    • We are a thriving counselling practice seeking part time associates to join our team.
    • Demonstrated skill in clinical decision-making and collaborative leadership required; previous experience providing clinical support, consultation, and…
    • Experience in the utilization and analysis of clinical data.
    • Quality Assurance activities are key to monitoring and sustaining clinical practice and the Quality…
    • Experience in clinical research is an asset.
    • Our team is committed to clinical excellence and a patient-centered approach.
    • Paid time off and holidays.
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    • Maintain high standards of clinical practice, ethics, and regulatory compliance.
    • Ongoing clinical supervision and professional development opportunities.
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Career Resources:

Clinical Research Coordinator, Sr.
Hamilton Medical Research Group
Hamilton, ON L8L 5G4
$35–$45 an hour
Full-time
Apply now

Job details

Here’s how the job details align with your profile.

Pay

$35–$45 an hour

Job type

Full-time

Benefits

Pulled from the full job description
Extended health care

Full job description

Job Description

We are currently seeking a full-time (8 to 4, Monday to Friday) Clinical Research Coordinator, for our downtown Hamilton location.

Responsibilities include recruitment of study participants (e.g. identify and screen potential subjects, obtain informed consent); coordination of patient visits schedules as per study protocol; execution of all aspects of study visit (e.g. questionnaires, sample collection, including processing and shipment of samples according to clinical protocol). The Clinical Research Coordinator plans, implements and coordinates aspects of data collection, source documentation and data entry per policy and ICH/GCP guidelines; executes study-related administrative tasks, such as collection of regulatory documents, creation of investigator study files, and ethics submissions.

QUALIFICATIONS:

  • Bachelors Degree in health-related field, or equivalent
  • At minimum, 3 years clinical and/or professional experience
  • Up to 1 year clinical research experience preferred; experience in recruiting patients for research studies or clinical trials
  • Knowledge of ICH/GCP guidelines
  • Knowledge of IATA shipping regulations and basic laboratory procedures an asset
  • Certification as a Clinical Research Professional, preferred
  • Excellent organizational and time management skills required
  • Excellent interpersonal, verbal and written communication skills
  • Ability to set priorities and work independently with accuracy in a multitasking environment
  • Strong Proficiency with MS Office software, Word, Excel, Outlook

Phlebotomy and/or ECG skills considered an asset.

Must be able to work independently with little supervision, as well as part of a larger team.

Additional compensation based on performance.

Job Type: Full-time

Pay: $35.00-$45.00 per hour

Benefits:

  • Extended health care

Experience:

  • clinical research: 2 years (required)

Licence/Certification:

  • GCP certification or equivalent (required)

Work Location: In person

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