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
