Job Summary:
We are looking for a permanent full-time Clinical Research Manager with extensive clinical trial management experience. We are team-oriented and believe in continued learning and professional development of all our staff. If you are highly motivated, committed to continuing professional development, work well in a team environment, have excellent communication, leadership, organizational, critical reasoning, and problem-solving skills, we want to hear from you!
Duties
- Lead clinical trial start-up work
- Contract preparation in collaboration with our legal partners
- Budget preparation and negotiation
- Creating, improving and monitoring site source documentation
- Ethics and other regulatory submissions to Health Canada
- Experience with site audits
- Routine invoicing based on the approved budget
- Responsible for coordinating and implementing all study-related activities such as initiating timely start-up, navigating strict eligibility criteria, and ensuring clean data is entered accurately and inline with monitoring requirements.
Requirements
- Degree in sciences field, preferably biomedical science, biology, biochemistry, health systems management, statistics
- Minimum 2-3 years of clinical research experience required.
- Recent experience conducting clinical trials.
- Documented experience with regulatory and ethics submissions.
- Knowledge and ability to do budgeting and invoicing for studies that are ongoing.
Job Type: Full-time
Pay: $37.50-$39.50 per hour
Expected hours: No more than 42 per week
Additional pay:
- Overtime pay
- Signing bonus
Benefits:
- Company events
- Dental care
- Extended health care
- Flexible schedule
- On-site parking
- Store discount
- Vision care
Flexible language requirement:
Schedule:
Education:
- Bachelor's Degree (required)
Experience:
- Budgeting: 2 years (preferred)
- Data collection: 2 years (required)
- Medical terminology: 2 years (required)
Work Location: In person
