Job opportunity
Research Coordinator Engineering and science : University of Alberta · Edmonton · Closes Tue, Nov 17
Avenue.io Inc.
This competition is open to all applicants; however, internal applicants will be given priority consideration based on minimum qualifications, or a combination of experience, skills, and abilities before external applicants are considered.
This position has a term length of1 year plus 1 day.
Location
- This role is in-person. Work primarily takes place at North Campus Edmonton.
The purpose of this position is to provide support to research support in the Department of Psychiatry, ranging from in-house investigator research to industry-sponsored research. Under the direction of the Academic Department Manager. This position is diverse and complex, with some standard procedures and day-to-day research operations, procedures and protocols, as well as the development of new procedures and techniques, and independent problem-solving. This position is responsible for coordinating various investigator-initiated and industry-sponsored research studies; therefore, work is done on an independent schedule with minimal supervision.
Participates in protocol management: reviews and adheres to multiple research protocols
Assists investigators with the preparation of documents for ethics submission (consents, protocols, study progress updates, adverse events reporting)
Assembles study specific source documents and updates study binders to ensure regulatory documentation is maintained to meet study requirements
In collaboration with the Principal Investigator, conducts screening and recruitment of potential study participants; including obtaining consent, performs study specific assessments pre- and post-operatively as required/appropriate
Provides instruction/teaching to study participants regarding study participation, protocol requirements, follow- up schedule, the use of data collection tools
Conducts patient follow-up, data collection, case report form (CRF) completion, study monitoring, data query resolution; promotes patient's adherence to the study and monitors patient safety in relation to study protocols
Provides ongoing written and oral reporting with the University Health Ethics Research Office (ARISE) and Northern Alberta Clinical Trials and Research Centre (NACTRC); investigators and industry sponsors
Works with investigators to notify departments regarding study termination/compliance; ensures appropriate retention of study files/materials
Conducts daily aspects of trials according to defined study protocols
Works with investigators and lead study sites regarding study termination, compliance, ensures appropriate retention of study files and materials
Reports adverse events promptly and accurately as described by the research protocol
Prepares for and assists with site visits by monitors during the study and once studies are closed out
Data collection for quality improvement
Assists Principle Investigators with the financial maintenance of approved projects
Ensure the GCP guidelines are followed
Post-secondary degree in Biological Science, Epidemiology, Health Sciences; equivalent combination of research experience and education may be considered
2 -3 years' experience with clinical trials an asset
Completion of NACTRC research coordinator course considered an asset
Completion of Society of Clinical Research Associate (SOCRA) certification considered an asset
Previous experience recruiting patients and research experience involving patients.
This position offers a comprehensive benefits package.
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Apply on source site This position has a term length of1 year plus 1 day.
Location
- This role is in-person. Work primarily takes place at North Campus Edmonton.
The purpose of this position is to provide support to research support in the Department of Psychiatry, ranging from in-house investigator research to industry-sponsored research. Under the direction of the Academic Department Manager. This position is diverse and complex, with some standard procedures and day-to-day research operations, procedures and protocols, as well as the development of new procedures and techniques, and independent problem-solving. This position is responsible for coordinating various investigator-initiated and industry-sponsored research studies; therefore, work is done on an independent schedule with minimal supervision.
Participates in protocol management: reviews and adheres to multiple research protocols
Assists investigators with the preparation of documents for ethics submission (consents, protocols, study progress updates, adverse events reporting)
Assembles study specific source documents and updates study binders to ensure regulatory documentation is maintained to meet study requirements
In collaboration with the Principal Investigator, conducts screening and recruitment of potential study participants; including obtaining consent, performs study specific assessments pre- and post-operatively as required/appropriate
Provides instruction/teaching to study participants regarding study participation, protocol requirements, follow- up schedule, the use of data collection tools
Conducts patient follow-up, data collection, case report form (CRF) completion, study monitoring, data query resolution; promotes patient's adherence to the study and monitors patient safety in relation to study protocols
Provides ongoing written and oral reporting with the University Health Ethics Research Office (ARISE) and Northern Alberta Clinical Trials and Research Centre (NACTRC); investigators and industry sponsors
Works with investigators to notify departments regarding study termination/compliance; ensures appropriate retention of study files/materials
Conducts daily aspects of trials according to defined study protocols
Works with investigators and lead study sites regarding study termination, compliance, ensures appropriate retention of study files and materials
Reports adverse events promptly and accurately as described by the research protocol
Prepares for and assists with site visits by monitors during the study and once studies are closed out
Data collection for quality improvement
Assists Principle Investigators with the financial maintenance of approved projects
Ensure the GCP guidelines are followed
Post-secondary degree in Biological Science, Epidemiology, Health Sciences; equivalent combination of research experience and education may be considered
2 -3 years' experience with clinical trials an asset
Completion of NACTRC research coordinator course considered an asset
Completion of Society of Clinical Research Associate (SOCRA) certification considered an asset
Previous experience recruiting patients and research experience involving patients.
This position offers a comprehensive benefits package.
#J-18808-Ljbffr