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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 clinical research experience is considered an asset.
    • Clinical research: 1 year (preferred).
    • Previous clinical research experience is an asset; however,…
    • Strong knowledge of research regulations and ethics processes.
    • Minimum 5 years relevant experience in clinical research operations.
    • View all Halton Healthcare jobs - Oakville jobs - Clinical Research Specialist jobs in Oakville, ON
    • Salary Search: Manager, Clinical Research salaries in Oakville, ON
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    • Reporting to the Team Lead, Ultrasound, the Clinical Education Lead ensures a varied and complete clinical experience for Ultrasound students.
    • And administering structured clinical interviews and standardized outcome measures.
    • Coordinating research activities with clinical staff delivering the…
    • Assist in preparing study reports, protocols, and ethics submissions.
    • The successful candidate will play a key role in managing and supporting clinical research…
    • The RN practices in accordance with the code of ethics of the CNO, CNA, and CFAS.
    • Practises in accordance with the code of ethics and standards as set by CNO,…
    • Collaborate with Laboratory Managers, Coordinators, Quality Managers, Professional Practice Leaders, Technical Specialists, physicians, and clinical teams.
    • Strong work ethic and good attendance record required.
    • In addition to operational and clinical oversight of integrated clinical services, this Manager…
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    • " Superior work ethic, professionalism and reliability; demonstrated commitment to providing outstanding customer/client service;
    • The clinical pharmacist will be responsible for supporting the development and implementation of clinical programs for the organization and supporting the…
    • Identify, develop and implement an Integrated Treatment Plan (ITP) based on the evaluation of clinical risk and need through the completion of the Short-term…
    • To work closely with the clinical team to facilitate residents’ move in and transfers where applicable;
    • Reporting to the Health and Wellness Manager, the…
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    • To work closely with the clinical team to facilitate residents’ move in and transfers where applicable;
    • Part-Time Unregulated Care Provider (UCP) - Days &…
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    • Park Place Retirement Residence - 110 Central Park Drive…
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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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