Clinical Research jobs in Winnipeg, MB
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Clinical Research / Clinical Trials Co-ordinator
Easily applyNewConfidentialWinnipeg, MB- Full-time
- ; conducts telephone and/or clinical recruitment interviews to collect data using established criteria; coordinates patient visits schedule as per study…
- University of ManitobaWinnipeg, MB
- Full-time +1
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- University of ManitobaWinnipeg, MB
- Full-time
- To support Canadian pandemic preparedness research and development, the University of Manitoba Faculty of Science is developing a new 21,000 sq.
View similar jobs with this employerUniversity of ManitobaWinnipeg, MB- Full-time +1
- The successful candidate will maintain a robust, externally funded program of research that is embedded within clinical practice and responsive to the needs and…
- University of ManitobaWinnipeg, MB
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- University of ManitobaWinnipeg, MB
- Full-time +1
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- University of ManitobaWinnipeg, MB
- Full-time +1
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- University of ManitobaWinnipeg, MB
- Full-time
- A personal statement including your positionality, demonstrated commitment and approach to issues pertaining to anti-racism and social justice (including…
- University of ManitobaWinnipeg, MB
- $70,000 a year
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- University of ManitobaWinnipeg, MB
- Full-time +1
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- University of ManitobaWinnipeg, MB
- Full-time +1
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- University of ManitobaWinnipeg, MB
- Full-time +1
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- University of ManitobaWinnipeg, MB
- Full-time
- Strong background in machine learning and deep learning approaches, preferably with experience in foundation models.
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- University of WinnipegWinnipeg, MB R3B 2E9
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- University of WinnipegWinnipeg, MB
- Full-time
- Weekends as needed
- We welcome applications from all qualified individuals and encourage women, racialized persons, Indigenous persons, persons with disabilities, and 2SLGBTQ+…
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Clinical Research / Clinical Trials Co-ordinator - job post
Confidential
Winnipeg, MB
Full-time
Job details
Job type
- Full-time
Location
Winnipeg, MB
Full job description
Seeking a Clinical Research Coordinator to join our growing team. The successful candidate will work under the direction of the Investigator, Sub-Investigator, and Senior Clinical Research Coordinator, collaborating with the research team in the following:
- Plans, implements, and coordinates all aspects of data collection and source documentation, as per protocol and guidelines
- Identifies problems using assessment skills and reports any abnormalities to the Study Investigator or Sub-Investigator
- Executes study-related administrative tasks such as collection of regulatory documents, ethics submissions, etc.; conducts telephone and/or clinical recruitment interviews to collect data using established criteria; coordinates patient visits schedule as per study protocol
- Ensures that all follow in up information is complete and document according to processes and protocols and all communication is up to date and accurate
- Executes all aspects of study visit (e.g. assessment, adverse events, monitoring safety, medication, questionnaires, sample collection, processing and shipment of samples) according to protocol.
- Participates in meetings including SIV’s, Study monitor visits and Study Close out visits.
The successful candidate will have related education, experience in Clinical Research or a related field, be highly organized, and able to work in an extremely fast paced environment. Superior communication skills and the ability to work as a member of a team are essential.
Job Type: Full-time
Work Location: In person
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