Clinical Trials Coordinator
1 day ago
About the Role:
We are seeking a highly skilled Clinical Trials Specialist to join our team at Canadian Myeloma Research Group.
Job Summary:
This is a permanent full-time position, working 35 hours per week, Monday through Friday, from 8:00 am to 4:00 pm. The successful candidate will have a minimum of two years of experience and a Bachelor of Science degree or equivalent.
Main Responsibilities:
- Study management, including coordination, data collection, and project management
- Clinical trial monitoring according to developed plans and SOPs
- Clinical database development and maintenance
- Protocol development, writing, and amendments
- Regulatory compliance with ICH-GCP, Health Canada, FDA, and US Federal Code
- Effective communication with various sites, staff, and sponsors at all levels
Skills and Qualifications:
- Experience managing and monitoring oncology trials
- Database development skills, preferably with Medidata Rave
- Demonstrated proficiency in English and French, with excellent oral and written communication skills
- Excellent organizational and prioritization skills, with the ability to learn quickly and independently
- Ability to work under pressure, maintain attention to detail, and produce high-quality work while meeting deadlines
- Exercise initiative and good judgment, with the ability to multi-task and adapt to changes
Salary: $65,000 - $85,000 per annum, depending on experience.
Benefits:
- A competitive salary package
- A comprehensive benefits program
- Ongoing professional development opportunities
Location: Our office is located in [location], but we offer remote work options.
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