Clinical Research Coordinator
2 weeks ago
At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.
**The Role**
Toronto Memory Program is looking for a Clinical Research Coordinator to manage clinical research protocols. This individual will work directly with the investigators, and other research staff to ensure protocol visits are being conducted according to ICH GCP guidelines.
**This Clinical Research Coordinator role will be based in Toronto, ON (North York) and is a full time position.**
**Responsibilities**:
- Comprehend study design of each protocol that is assigned
- Perform procedures in compliance with the study protocol
- Collect and record study data in source documents via electronic system (CRIO)
- Manage study related activities
- Adherence to protocol requirements
- Review laboratory data
- Assess and document compliance
- Manage investigational product
- Assess, record, and report Adverse Events as outlined in the protocol
- Manage/train ancillary staff
**Requirements**:
- Experience and training in conducting clinical trials with knowledge of ICH GCP OR
- Two years of college in a health-related program or LPN OR
- Bachelor's degree in a health or scientific related program
- A thorough understanding of regulatory requirements
- Experience performing clinical assessments, including but not limited to obtaining vital signs, EKGs, blood draws, processing/shipping lab specimens
- Experience with CRIO (Clinical Trial Management System) is a plus
- Experience with administering vaccines is a plus
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Clinical Research Coordinator
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Toronto, Canada Headlands Research Full timeOverview: **The Role** Toronto Memory Program is looking for a Clinical Research Coordinator to manage clinical research protocols. This individual will work directly with the investigators, and other research staff to ensure protocol visits are being conducted according to ICH GCP guidelines. **This Clinical Research Coordinator role will be based in...
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