Bayshore Evening Nursing Roles Available

About Our ClinicAlzheimer's disease (AD) is the most common type of dementia, making up approximately 70% of all cases. Those over the age of 65 are at a higher risk to develop AD. It diminishes cognitive, verbal and physical abilities by destroying brain cells.

This in turn affects our ability to think, to learn new things, and to remember. Many scientific experts are working to ameliorate our understanding of this devastating disease, thus searching to find more effective treatments.Our clinics partner with pharmaceutical companies to conduct Phase II and III clinical trials for Alzheimer's Disease. Our unique contribution will revolutionize the fight against the disease.

We provide care to patients, generate knowledge for the scientific community, continue to improve support, and access to clinical research.SummaryUnder the authority of the Director of Clinical Research Operations, the incumbent is responsible for the implementation and execution of the procedures in research protocols, including support in the development, organization, management, and follow‑up of research programs. This position is also responsible for providing administrative service in terms of development, organization, management, and follow‑up of various research programs.Specific TasksMaster the latest versions of documents related to the research programsParticipates in the creation and verification of the file source template for each research programPrepare and complete the subject’s source files for study visits of the research programs and ensure follow‑up and final approval of the subject’s study source files with the PI/Sub‑IEnsure the planning and smooth running of visits related to research programsWrite study visit summary notes and get them approved by PI/Sub‑IDispense study medicationEnsure subject’s compliance to study medicationMaster all aspects of the study subject source file documentation as per protocolEnsure the remittance and follow‑up of reimbursements for study subjects and their study partnersCreate, maintain and follow‑up on various study logs (study statistics, reimbursements, etc.)Respond to queries and follow‑ups following visits by study monitorsComplete various medical forms (laboratory, MRI, PET, etc.)Update electronic patient recordsCollaborate with various study partners (monitors, pharmacists, suppliers, etc.)Maintain up‑to‑date training specific to the various research programs as well as general trainingDevelop tools and work methods (tables, documents, statistics, etc.)Perform work in accordance with the provisions of the Occupational Health and Safety Act and Regulations and all company policies and procedures related to Occupational Health and SafetyPerform other related duties as assignedRequirementsVocational TrainingIs a member in good standing of the College of Nurses of OntarioA post‑secondary degree or diploma in nursing is required, or a combination of education, training and experience deemed equivalentExperienceMinimum of two (2) years of experience in acute care, including intravenous placement and management of discomfort and allergiesExperience in medical research would be an assetSkills, Abilities and CompetenciesKnowledge of current computerized systems (MS Office Suite)Good oral and written communication skills in French and EnglishMastery of good puncture and infusion techniquesAbility to manage prioritiesOffering service adapted to the target clienteleAbility to work under pressureSense of organization and time managementAdapting to changeThoroughnessTeam spiritVersatilityResourcefulnessResponsibleProfessionalismHigh quality in terms of confidentiality and discretion#J-18808-Ljbffr