Clinical Research Coordinator
8 months ago
We are conducting the Screening rounds and an assessment sessions on behalf of our Clients for the Clinical Research coordinator roles. If qualified, your roles and responsibilities would be as follows:
**Duties**:
- Coordinate and oversee clinical research studies from start to finish
- Ensure compliance with study protocols, regulations, and ethical guidelines
- Recruit and screen potential study participants
- Obtain informed consent from participants and explain study procedures
- Collect and manage data, including medical records, lab results, and participant questionnaires
- Schedule and coordinate study visits, procedures, and tests
- Assist with data analysis and interpretation
- Collaborate with the research team, including physicians, nurses, and other healthcare professionals
- Maintain accurate and up-to-date study documentation
- Adhere to Good Clinical Practice (GCP) guidelines
**Requirements**:
- Bachelor's degree in a related field (e.g., healthcare, life sciences)
- Knowledge of medical terminology and clinical research processes
- Experience in data management and analysis
- Strong organizational skills with attention to detail
- Phlebotomy skills or willingness to learn
- Ability to critically analyze research data and identify trends or patterns
- Excellent communication skills, both written and verbal
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)
**Job Types**: Seasonal, Freelance, Internship / Co-op
Pay: $46,520.25-$55,731.57 per year
Flexible Language Requirement:
- French not required
Schedule:
- Monday to Friday
**Education**:
- Bachelor's Degree (preferred)
**Experience**:
- medical writing: 1 year (preferred)
Work Location: In person
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