Clinical Research Coordinator

2 weeks ago

Toronto, Canada Headlands Research Full time

**Overview**:
**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

**Qualifications**:

- 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
- AND
- 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
- At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. We’re an exceptional family of next-generation clinical trial sites, integrating cutting edge technology and high-quality support services, and significantly expanding participant engagement Founded in 2018, our company operates 20+ clinical trial sites in the US and Canada with rapid plans for expansion.

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