Research Specialist at Dentons, a global law firm, focusing on AI - enhanced legal research and team collaboration across Canadian offices.
About the role
- Clinical Research Associate ensuring sites comply with clinical study protocols at IQVIA. Performing monitoring visits and managing study progress across various locations.
Responsibilities
- Perform monitoring and site management work to ensure that sites are conducting the study(ies).
- Perform site monitoring visits in accordance with contracted scope of work and Good Clinical Practice.
- Work with sites to adapt, drive, and track subject recruitment plan.
- Administer protocol and related study training to assigned sites.
- Evaluate the quality and integrity of study site practices.
- Manage the progress of assigned studies by tracking regulatory submissions and approvals.
- Ensure copies/originals site documents are available for filing in the Trial Master File.
Requirements
- Bachelor's Degree in scientific discipline or health care preferred.
- Requires at least 2 years of on-site monitoring experience.
- Equivalent combination of education, training and experience may be accepted in lieu of degree.
- Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.
- Good therapeutic and protocol knowledge as provided in company training.
- Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint.
- Written and verbal communication skills including good command of English language.
- Organizational and problem-solving skills.
- Effective time and financial management skills.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
Benefits
- Health insurance
- Retirement plans
- Paid time off
- Flexible work arrangements
- Professional development opportunities
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