0000043888 - Coordinator I, Clinical Research, Tft (Winnipeg)

0000043888 - Coordinator I, Clinical Research, Tft (Winnipeg)

07 Aug
|
Beam Radiology
|
Winnipeg

07 Aug

Beam Radiology

Winnipeg

About Beam RadiologyBeam Radiology is a physician-led diagnostic imaging and specialty care organization committed to compassionate patient care and service excellence for our referring practitioners. Our patients always come first.Our sub-specialty trained radiologists provide a comprehensive range of diagnostic imaging, obstetrical, interventional, and pain management services. Working collaboratively across multidisciplinary teams; including physicians, imaging technologists, nurses, researchers, and administrative professionals; we strive to deliver anexceptional patient and practitioner experience. Beam is also actively involved in clinical research that advances care and improves lives in our communities.The OpportunityBeam Radiology is seeking a motivated Clinical Research Coordinator to join our interventional pain management research team of physicians, imaging technologists, and clinical research specialists.The Research Coordinator is a health care skilled who functions as an administrator, coordinator, educator, and researcher, ensuring research activities are conducted with excellence, integrity and compliance. This role supports both investigator initiated and industry sponsored clinical trials within a community-based clinic setting.This role reports to the Clinical Research Manager and is a full-time 12 month role with the possibility of extension (subject to funding).Key ResponsibilitiesPatient & Research SupportUnderstand and implement basic research procedures with respect to informed consent,



data collection and reporting following ICH-GCP under the guidance and supervision of the Clinical Research Manager.Assist in determining eligibility for protocols based on medical history and assessment information in consultation with the Research TeamCollect data for interventional pain management research participants using in-person data collection tools and electronic health record reviewsImplement protocol required activities ensuring excellence in delivery of the research processWork collaboratively with interventional radiologists, nurses, imaging technologists, operational and administrative staffWork within the guidelines of privacy and ethical standardsBe comfortable in a diagnostic imaging and interventional pain management settingAdministrative ResponsibilitiesHave an extensive knowledge of ongoing research projectsPrepare participant research charts including source documentationMaintaining accurate and detailed records of patient files to ensure they fit all criteria to be enrolled in specific clinical trialsEnsure data entry is accurate and precise and is entered in a timely manner according to research protocolsMonitoring & Regulatory SupportPreparing and filing study documentation prior to visitEnsuring the monitor has everything required for the visit under the guidance of the Clinical Research ManagerCommunication with monitor to ensure an effective visitObtaining proper documentation before, during and after visit, as requiredFacilitate regulatory document completion and updates as necessaryOngoing maintenance of participant binders and TMFEnsure all required documentation is available and filed properlyCommunication & CollaborationWork collaboratively with the Research Team and all clinical departmentsDevelop and maintain communication with various stakeholdersQualificationsUndergraduate degree in life sciences and/or clinical research experienceMinimum two years’ experience in a clinical research positionSpecialized certification - TCPS 2 and ICH-GCP E6(R3) certificationSoCRA or ACRP certification an asset, but not requiredOrganized and efficient individual with strong attention to detailExperience entering data in EDC formats is an asset, but not requiredIntermediate to advanced skills in Microsoft Office Suite (Word, Outlook, Excel, PowerPoint), Internet skillsDemonstrated ability to work independently and as part of a teamWorking ConditionsFull-time role, typically Monday to Friday based on operational needsThere will be occasional weekend hours: approximately 1 day per month with advance notice.Primarily in-person across Beam Radiology clinic locations in CalgaryOccasional travel between clinic sitesCompensation & Total RewardsCompetitive compensation commensurate with qualifications and experienceComprehensive health, dental, disability, and extended health benefits (including STD and LTD)Health and Wellness Spending AccountsEmployee and family assistance support programsRRSP program with employer matchingPaid time off (vacation and sick leave)Free on-site parkingContinuing education courses and professional development incentivesCompany events and team-building activitiesEquity, Diversity & InclusionBeam Radiology is an equal opportunity employer. We are committed to creating an inclusive, respectful, and supportive workplace where everyone feels valued and empowered to succeed.Accommodations are available throughout the recruitment process. Applicants requiring accommodation are encouraged to advise us accordingly.We thank all applicants for their interest; however, only those selected for further consideration will be contacted.#J-18808-Ljbffr

📌 0000043888 - Coordinator I, Clinical Research, Tft (Winnipeg)
🏢 Beam Radiology
📍 Winnipeg

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