Clinical Research Associate ensuring sites conduct studies and reporting data accurately. Monitoring, site management, and collaboration with the study team.
About the role
- Senior Clinical Research Associate executing and supervising clinical trials from Phase I to IV. Collaborating closely with clinical trial directors and assessing site capabilities in Canada.
Responsibilities
- Participates in the planning and conduct of Phase I–IV clinical trials
- Monitors the progress of clinical investigations through site monitoring visits
- Ensures clinical trials are conducted in accordance with Good Clinical Practice (GCP)
- Collaborates with the clinical trial director and/or the lead CRA
- Conducts study initiation activities and provides training
- Reviews the quality and integrity of clinical data through source data verification
- Prepares monitoring reports within the timelines defined in IQVIA SOPs
Requirements
- 3 years of monitoring experience
- Strong knowledge of the clinical research process
- Four or more years of experience in oncology and/or medical devices
- Excellent written and verbal communication skills
- University degree in life sciences or healthcare (BS/BA/BSc) with a minimum of four years' experience in monitoring/site management
- Must be able to travel domestically and internationally approximately 65%–85%
- Valid driver's license
- Computer skills, including proficiency in Microsoft Word, Excel, and PowerPoint
Benefits
- Incentive plans, bonuses and/or other forms of compensation may be offered, in addition to a range of health, wellness, and other employee benefits
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