Shelly Rempel-Rossum

Manage and support the review of research protocols to ensure they comply with ethical standards and regulations . This involves coordinating submissions, providing administrative and expert support to researchers and the board, maintaining records, and ensuring the day-to-day operations of the Research Ethics Board (REB) are smooth. Key duties include communicating with researchers, conducting administrative reviews, and staying updated on relevant policies and legislation.

• Implemented evidence-based practices to enhance patient outcomes and operational efficiency.
• Utilized critical thinking skills to prioritize nursing interventions based on patients'' acuity levels and individual needs.
• Conducted thorough patient assessments to identify changes in condition, promptly notifying physicians and initiating appropriate interventions when necessary.
• Enhanced patient satisfaction by providing compassionate, holistic nursing care that addressed physical, emotional, and spiritual needs.
• Improved patient outcomes by implementing evidence-based nursing interventions and individualized care plans.
• Provided support for patients'' families during difficult medical decisions or end-of-life care, serving as a liaison between the healthcare team and loved ones.

• Coordinated Winnipeg site for a large multi-centre NIH funded stop smoking study - Lung HEalth Study
• Coordinated clinical trials to ensure compliance with research protocols and regulatory guidelines.
• Monitored patient/participant progress, documenting outcomes and adverse events meticulously.
• Established effective working relationships with external partners, including sponsors, regulatory agencies, and other healthcare institutions involved in collaborative research projects.
• Improved retention rates among study participants by providing ongoing support and education throughout the duration of the trial period.
• Served as a liaison between investigators, sponsors, and institutional review boards to facilitate communication and resolve issues promptly.
• Conducted regular assessments of study participants'' health status, documenting any adverse events or changes accordingly.
• Gathered, processed, and shipped lab specimens.
• Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
• Collected, evaluated, and modeled collected data.