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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.
    • The successful candidate will play a key role in managing and supporting clinical research activities.
    • Support clinical research activities, including patient…
    • Clinical research or research administration;
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    • Experience with an accepted clinical data capture and management system preferred.
    • Plan and manage deliverables and timelines in accordance with clinical trial…
    • The ideal candidate is a critical thinker who can pivot seamlessly between the rigid requirements of research and the dynamic needs of a clinical practice.
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    • Compile documentation for qualification of clinical sites.
    • To facilitate the implementation and management of the clinical trial.
    • MSc with clinical research experience or, a BSc or LPN with extensive clinical research experience preferred.
    • Schedule and conduct clinical research visits and…
    • Software programming experience relevant to the programming languages and design applications in use in clinical research.
    • Experience in clinical research, call center support, pharmaceutical sciences.
    • At least five years of experience in clinical trial data processing and…
    • Oversees and coordinates as needed data management using the relevant research methodology while properly handling all research material.
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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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