Clinical Research Nurse Specialist

3 weeks ago

Hamilton, Ontario, Canada McMaster University Full time
Job Summary:

The Clinical Research Nurse (I) is a key member of our research team, responsible for planning, assessing, implementing, and evaluating protocol procedures. This role ensures that all aspects of the study protocol are adhered to, and coordinates daily operations of clinical research studies.

Purpose and Key Functions:
  • Develop and implement clinical research protocols, working closely with a team to ensure successful project execution.
  • Participate in the development and authoring of research protocols, utilizing expertise in research principles and practices.
  • Troubleshoot problems at all stages of project development and implementation, modifying protocols or project procedures as needed.
  • Conduct patient assessments to determine eligibility for research studies, ensuring accurate and timely data collection.
  • Monitor patients for adverse reactions, responding promptly and appropriately.
  • Communicate effectively with patients, family members, and caregivers, educating them on the disease process and benefits of clinical studies.
  • Liaise with clinic centers and remote sites, ensuring seamless coordination and communication.
  • Analyze and process information to ensure accuracy and appropriateness of patient management.
  • Apply research methodology and handle research materials in accordance with established protocols, policies, and procedures.
  • Conduct study-specific assessments to determine patient suitability and disease acuity.
  • Apply scientific principles to review, critically appraise, and interpret published literature.
  • Empathize with study patients, providing attentive and compassionate care.
  • Recruit patients and enlist agencies to refer patients, ensuring a diverse and representative participant pool.
  • Design promotional strategies and materials to encourage participation and support for research studies.
  • Facilitate focus group sessions with study patients, gathering valuable feedback and insights.
  • Write sections of scientific papers, funding proposals, abstracts, and Research Ethics Board submissions.
  • Design and develop various forms, data reports, and letters required for the study.
  • Document and analyze patient responses and adverse events, ensuring accurate and timely reporting.
  • Maintain patient consult notes, assessments, drug accountability logs, charts, and histories, adhering to established regulations.
  • Plan and coordinate studies across multiple sites, ensuring efficient and effective project execution.
  • Develop estimates of time and resources for research projects, ensuring accurate and realistic projections.
  • Use statistical software to analyze data and interpret results, informing study decisions and outcomes.
  • Complete various calculations, such as medication doses and safety values, ensuring accurate and timely reporting.
  • Develop presentations and present information and training sessions to study personnel and patients, promoting knowledge sharing and collaboration.
  • Retrieve and respond to results of diagnostic tests, ensuring timely and accurate communication.
  • Keep study participants informed of study progress through regular reports and newsletters, maintaining transparency and engagement.
  • Implement and maintain study budgets, creating financial projections and adjusting budgets as needed.
  • Exercise appropriate controls, monitor, and reconcile accounts, ensuring accurate and timely financial reporting.
  • Collect, verify, evaluate, and record all patient study data, maintaining confidentiality and adhering to established regulations.
  • Update and maintain information in various databases and spreadsheets, ensuring accurate and timely data management.
  • Gather, compile, and submit all pertinent documents, such as licenses and curriculum vitae, prior to study initiation.
  • Arrange for the safe and orderly exit of patients from the study, ensuring a smooth and respectful conclusion.
  • Accountable to the College of Nurses of Ontario for all actions taken with study patients, practicing according to the Regulated Health Professions Act and Standards of Practice for Nurses in Ontario.
  • Conduct literature searches, staying up-to-date with the latest research and developments in the field.
  • May be required to perform specific medical procedures, such as venipuncture and administering medication by injection, under the guidance of a qualified healthcare professional.
  • May be required to set up and monitor various medical devices, such as intravenous and electrocardiogram equipment, under the guidance of a qualified healthcare professional.
  • Collaborate with hospital administrators to facilitate the introduction of study protocol procedures within their departments, promoting seamless integration and coordination.
  • Coordinate the procurement of equipment, supplies, and data collection forms, ensuring timely and accurate delivery.
  • Inform patients and family members about study protocols and procedures, ensuring clear and concise communication.
  • Explain benefits, risks, and schedules prior to obtaining informed consent, ensuring that patients understand the study and its requirements.
  • Abide by and adhere to hospital partners' policies and procedures regarding various sources of information, such as health records and databases.
  • Maintain the confidentiality of patient files and study data, adhering to established regulations and guidelines.
  • File and maintain a variety of documents, such as source documentation, case report forms, and clinical records, according to established regulations.

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