Clinical Research Coordinator

3 weeks ago


Ottawa, Canada Red Maple Trials Full time

'''Job Summary:
**Duties**:

- Coordinate and oversee all aspects of clinical research studies
- Develop and maintain study protocols and ensure compliance with regulatory requirements
- Recruit and screen potential study participants
- Obtain informed consent from participants and explain study procedures
- Collect, record, and manage data in accordance with study protocols
- Conduct interviews, administer questionnaires, and perform physical assessments as required
- Coordinate with healthcare professionals, including nurses and physicians, to ensure smooth study operations
- Monitor participant safety and report adverse events to the appropriate authorities
- Assist with the analysis and interpretation of study data
- Maintain accurate and up-to-date documentation of all study activities

**Experience**:

- Previous experience as a Clinical Research Coordinator or similar role is preferred
- Strong knowledge of data management principles and practices
- Familiarity with medical terminology and ability to accurately interpret medical records
- Proficient in using electronic data capture systems for data entry and management
- Ability to supervise and train research staff as needed
- Excellent organizational skills with the ability to multitask and prioritize effectively
- Detail-oriented with strong analytical skills for data collection and analysis
- Experience in phlebotomy is a plus

If you are passionate about clinical research, have excellent attention to detail, and thrive in a fast-paced environment, we encourage you to apply. Join our team today'''

**Salary**: $20.00-$35.00 per hour

Expected hours: 40 per week

Schedule:

- Monday to Friday

**Experience**:

- Clinical Research: 1 year (preferred)

Work Location: In person

Expected start date: 2024-04-01



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