Clinical Research Coordinator

1 week ago

London, Canada Mediprobe Research Inc. Full time

_**Windermere Health Centre/Mediprobe Research seeking experienced coordinator for a private practice dermatology clinic performing sponsored and investigator-initiated research.**_

Tasks include patient recruitment, informed consent processes, basic study data collection and assisting the PI in capturing all required study data, as well as research appointment scheduling, and screen visit booking. Correspondence with sponsors/monitors/ethics board as needed. Interacting with study monitors to ensure all study visit activities are completed and documented as required.

25-35hr per week depending on clinic needs; M-F, no weekends; daytime hours only.

$22-28/hr
- Minimum: Bachelors degree, or recognized equivalent, in a health or science-related discipline
- Demonstrated experience with patient contact and informed consent in a clinical setting
- Understanding of regulated clinical trial data and regulatory tasks required
- Knowledge of ICH/GCP guidelines; current GCP certificate required
- Knowledge of IATA shipping regulations and basic laboratory procedures is an asset
- Phlebotomy skills an asset
- SoCRA/ACRP certification, other certification in clinical research is an asset
- Good proficiency with MS Office software, Microsoft Teams, Outlook

**Job Types**: Full-time, Part-time
Part-time hours: 25-35 per week

**Salary**: $22.00-$28.00 per hour

**Benefits**:

- Casual dress
- On-site parking

Flexible Language Requirement:

- French not required

Schedule:

- Day shift
- Monday to Friday

Ability to commute/relocate:

- London, ON N5X 2P1: reliably commute or plan to relocate before starting work (required)

Application question(s):

- Do you have an active GCP certificate?

**Education**:

- Bachelor's Degree (preferred)

Work Location: In person

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