Clinical Researcher
2 months ago
**Job Summary**
**Responsibilities**:
- Plan and execution clinical trials from initiation through completion.
- Monitor trial progress and ensure adherence to study protocols and regulatory guidelines.
- Collect, analyze, and interpret data using statistical software.
- Prepare and maintain study documentation including protocols, informed consent forms, and case report forms.
- Conduct site visits to assess compliance, data integrity, and overall trial conduct.
- Assist in the preparation of reports for regulatory submissions and presentations.
**Experience**:
- Bachelor’s degree in life sciences or a related field; advanced degree preferred.
- Previous experience in clinical research.
- Strong organizational skills with attention to detail.
- Excellent communication skills, both verbal and written.
- Ability to work independently as well as part of a collaborative team environment.
Join us in making a difference through innovative research that improves patient outcomes
**Job Type**: Part-time
Pay: $16.55-$50.00 per hour
Expected hours: 10 - 20 per week
**Benefits**:
- Casual dress
- Dental care
- On-site parking
- Paid time off
- Work from home
Application question(s):
- Have you previously written clinical research protocols and applied for ethics approval?
Work Location: Hybrid remote in Oakville, ON L6J 0B2
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