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Clinical Trials Coordinator
2 months ago
The role of a Clinical Research Associate involves overseeing and managing clinical trials within a university setting. This position requires a strong educational background and relevant experience in the field.
Qualifications- Education: A doctorate degree is essential.
- Experience: Candidates should have between 3 to 5 years of relevant experience.
This position is hybrid, allowing for a combination of remote and on-site work.
Key Responsibilities- Supervise laboratory and clinical personnel, including graduate students and research scientists.
- Provide strategic advice to senior management.
- Conduct administrative duties and produce comprehensive reports.
- Prepare research papers and educational materials.
- Deliver presentations at academic conferences and workshops.
- Monitor and compile research findings effectively.
- Offer mentorship to junior staff and students.
Experience in experimental or quantitative research is required, with a focus on medical specializations such as immunology and microbiology.
Compliance and SafetyA criminal record check is mandatory for this position.
Health and Long-Term Benefits- Health Benefits: Includes dental, disability, healthcare, paramedical services coverage, and vision care.
- Long-Term Benefits: Maternity and parental benefits are provided.
The expected work hours are 40 hours per week.
Screening QuestionsApplicants will be asked to confirm their availability for the start date, legal eligibility to work in Canada, willingness to relocate, and previous experience in the field.