Clinical Research Coordinator - ALS and Neuromuscular Research Group
University of Alberta•Edmonton, AB
•CA$59,842 - CA$80,796•Onsite
About The Position
The Clinical Research Coordinator is responsible for assisting and supporting the Clinical Research Manager in the overall operations and management of current and upcoming externally funded and Investigator-initiated drug studies and other neuromuscular/ALS research studies within the Division of Neurology. This position works as a contributing study team member with other research coordinators, physicians, lab personnel, and stakeholders of the research.
Requirements
- Assisting in the preparation of pre-study documentation
- Preparation of applications for Health Research Ethics Board approval
- Preparation of patient information and informed consent sheets
- Patient screening, interviewing and recruitment
- Obtaining patient informed consent
- Completing patient enrolment
- Conducting study visits and collection of study data
- Maintaining and dispensing drug supplies
- Completing case report forms
- Maintaining source documents
- Ensuring and maintaining site quality
- Ongoing Health Research Ethics Board Interaction and communication
- Collection of laboratory specimens
- Handling and shipping of laboratory specimens
- Documentation of safety events and notification of the Clinical Research Manager, Principal Investigator, and other authorities as required.
Responsibilities
- Assisting in the preparation of pre-study documentation
- Preparation of applications for Health Research Ethics Board approval
- Preparation of patient information and informed consent sheets
- Patient screening, interviewing and recruitment
- Obtaining patient informed consent
- Completing patient enrolment
- Conducting study visits and collection of study data
- Maintaining and dispensing drug supplies
- Completing case report forms
- Maintaining source documents
- Ensuring and maintaining site quality
- Ongoing Health Research Ethics Board Interaction and communication
- Collection of laboratory specimens
- Handling and shipping of laboratory specimens
- Documentation of safety events and notification of the Clinical Research Manager, Principal Investigator, and other authorities as required.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
Upload and Match Resume
What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
