Clinical Research Nurse

3 weeks ago

Hamilton, Ontario, Canada McMaster University Full time

Job Summary:

The Clinical Research Nurse is a key member of our research team at McMaster University, responsible for planning, assessing, implementing, and evaluating protocol procedures for clinical research studies. This role ensures that all aspects of the study protocol are adhered to, and coordinates daily operations to ensure smooth project execution.

Purpose and Key Functions:

  • Develop and implement clinical research protocols, working closely with the research team to ensure protocol adherence.
  • Participate in the development and authoring of research protocols, ensuring that all necessary information is included.
  • 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 that all necessary information is collected.
  • Monitor patients for adverse reactions, responding appropriately to ensure patient safety.
  • Communicate with family members and caregivers, educating them about the disease process and the benefits of clinical studies.
  • Liaise with clinic centres and remote clinic sites, ensuring seamless communication and coordination.
  • Process information, recognizing problems with patients and intervening appropriately to ensure patient well-being.
  • Analyze and process information to ensure accuracy and appropriateness of patient management.
  • Ensure that research methodology is applied, and all research material is handled in accordance with established protocols, policies, and procedures.
  • Conduct study-specific assessments of patients to determine suitability for projects and degree of disease acuity.
  • Apply specialized knowledge and scientific principles to review, critically appraise, and interpret published literature.
  • Empathize with study patients, being attentive to their needs and providing support.
  • Recruit patients and enlist agencies to refer patients, ensuring a diverse and representative participant pool.
  • Review referrals and track intakes from various referral sources, ensuring efficient participant management.
  • Design promotional strategies and related materials to encourage participation and support for research studies.
  • Facilitate focus group sessions with study patients, ensuring that their voices are heard and valued.
  • Write sections of scientific papers, funding proposals, abstracts, and Research Ethics Board submissions, ensuring that all necessary information is included.
  • Design and develop various forms, data reports, and letters required for the study, ensuring accuracy and completeness.
  • Document and analyze patient responses and adverse events, ensuring that all necessary information is recorded.
  • Document and maintain patient consult notes, assessments, drug accountability logs, charts, and histories on each patient, ensuring accurate and up-to-date records.
  • Plan and coordinate studies across multiple sites, ensuring seamless execution and coordination.
  • Develop estimates of time and resources for research projects, ensuring that all necessary resources are allocated.
  • Use statistical software to analyze data and interpret results, ensuring that all necessary information is included.
  • Complete various calculations, such as medication doses, safety values for clinical testing, and drug formulas, ensuring accuracy and precision.
  • Develop presentations and present information and training sessions to study personnel and patients, ensuring that all necessary information is communicated.
  • Retrieve and respond to results of diagnostic tests, ensuring that all necessary information is recorded.
  • Keep study participants informed of study progress through regular reports and newsletters, ensuring that all necessary information is communicated.
  • Implement and maintain study budgets, creating financial projections and making adjustments as needed.
  • Exercise appropriate controls, monitor, and reconcile accounts, ensuring that all necessary financial information is accurate and up-to-date.
  • Responsible for the accurate collection of relevant data, ensuring that all necessary information is recorded and maintained.
  • Collect, verify, evaluate, and record all patient study data, ensuring that all necessary information is included.
  • Update and maintain information in a variety of databases and spreadsheets, ensuring that all necessary information is accurate and up-to-date.
  • Gather, compile, and submit all pertinent documents, such as physician and nursing licenses, curriculum vitae for all staff involved in the study, Food and Drug Administration forms, and Research Ethics Board documents, prior to the start of a clinical study.
  • Arrange for the safe and orderly exit of patients from the study, ensuring that all necessary information is recorded and maintained.
  • Accountable to the College of Nurses of Ontario for all actions taken with study patients, ensuring that all necessary information is recorded and maintained.
  • Conduct literature searches, ensuring that all necessary information is included.
  • May be required to perform specific medical procedures, such as venipuncture, pipetting samples, and administering medication by injection, ensuring that all necessary information is recorded and maintained.
  • May be required to set up and monitor various medical devices, such as intravenous and electrocardiogram equipment, ensuring that all necessary information is recorded and maintained.
  • Collaborate with hospital administrators to facilitate the introduction of study protocol procedures within their departments, ensuring that all necessary information is recorded and maintained.
  • Coordinate the procurement of equipment, supplies, and data collection forms, ensuring that all necessary information is recorded and maintained.
  • Inform patient and family about study protocols and procedures, ensuring that all necessary information is communicated.
  • Explain benefits, risks, and schedules prior to obtaining informed consent, ensuring that all necessary information is communicated.
  • Obtain formal, informed, and signed consent, ensuring that all necessary information is recorded and maintained.
  • Abide by and adhere to hospital partners' policies and procedures with regards to various sources of information, such as health records and databases, ensuring that all necessary information is recorded and maintained.
  • Maintain the confidentiality of patient files and study data, ensuring that all necessary information is recorded and maintained.
  • File and maintain a variety of documents, such as source documentation, case report forms, and clinical records, according to established regulations, ensuring that all necessary information is recorded and maintained.

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