Clinical Research Coordinator
6 days ago
Responsibilities:
- Coordinate and oversee clinical research studies from start to finish
- Collect and record data accurately and efficiently
- Analyze research data and prepare reports for review
- Ensure compliance with study protocols, regulations, and ethical guidelines
- Collaborate with healthcare professionals, researchers, and study participants
- Schedule and conduct study visits, including phlebotomy (Must be able to collect and process blood samples)**:
- Maintain accurate and organized study documentation
- Assist with data management and quality control processes
- Experience giving immunizations is an asset
**Experience**:
- Previous experience in clinical research or a related field is preferred (min 1 year)*
- Knowledge of medical terminology and research methodologies
- Self started, able to work independently
- Strong attention to detail and organizational skills
- Excellent communication and interpersonal skills
- Proficient in data collection, analysis, and reporting software
This position is based out of a family doctors practice, it offers the opportunity to contribute to groundbreaking medical research while working in a collaborative and supportive environment.
RPN's, RN's and IMG's welcome to apply. Training will be provided.
Please note that this is not an entry-level position. Prior experience in clinical research or a related field is required.
**Job Types**: Full-time, Part-time
**Salary**: $25.00-$32.00 per hour
Expected hours: 30 per week
**Benefits**:
- Dental care
- Extended health care
- Paid time off
Flexible Language Requirement:
- French not required
Schedule:
- 8 hour shift
- Monday to Friday
- Weekends as needed
**Education**:
- Bachelor's Degree (preferred)
**Experience**:
- clinical research: 1 year (required)
Ability to Commute:
- Toronto, ON M4S 1Y2 (required)
Ability to Relocate:
- Toronto, ON M4S 1Y2: Relocate before starting work (required)
Work Location: In person
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