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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.
    • Conducts research and analyzes various assignments/projects as directed for best practices and industry standards for continual improvement of return-to-work…
    • Professional Experience: At least 3 years of work experience in the medical field as an LPN or HCA.
    • If you have a passion for teaching and a wealth of…
    • Manages medical writing activities associated with individual studies, defining document strategy and coordinating medical writing activities within and across…
    • Experience preparing research reports, grant applications, and presentations.
    • Supervising research staff, graduate students, and trainees as appropriate.
    • API offers a generous paid time off (PTO) policy that includes vacation days, medical/personal days, and holidays.
    • Required travel between Edmonton API sites.
    • API offers a generous paid time off (PTO) policy that includes vacation days, medical/personal days, and holidays.
    • Strong oral and written communication.
    • API offers a generous paid time off (PTO) policy that includes vacation days, medical/personal days, and holidays.
    • Vendor/service contract oversight experience.
    • Understanding of ethical standards and regulations governing clinical research and patient care.
    • Opportunities to participate in clinical research involving…
    • Clinical research or research administration;
    • Experience with electronic medical records or electronic research systems is an asset.
    • Assist in research and development of statistical methodologies and processes.
    • Provide statistical expertise for design, analysis and reporting of clinical…
    • Perform literature searches to support senior medical writers.
    • Ensuring appropriate QC checks have been performed on the medical writing deliverables.
    • Reporting directly to the Director Non-Emergency Medical Transport, Ontario, the General Manager will play a key role in the strategy and business development…
    • Demonstrated knowledge of medical and scientific terminology.
    • Knowledge of research ethics, confidentiality, and documentation standards.
    • Supervise special techniques of specimen preservation and research and develop new applications.
    • Prepare for autopsies by obtaining patients' medical records…
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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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