Research Coordinator RN - Oncology Research (ACCRU) - Department of Research

Nova Scotia Health and IWK HealthHalifax, NS
CA$42 - CA$53Onsite

About The Position

The Research Coordinator – Registered Nurse (RN) coordinates research projects within Nova Scotia Health, including prescreening potential clinical trial participants, administering clinical trials, caring for participants (in the clinic setting, and on-call), and managing study documents and data. Under the direction of the Principal Investigator and the ACCRU Manager of Clinical Research Operations, they provide clinical leadership and ensure ICH GCP compliant, appropriate, coordinated nursing care by the study team. They deliver culturally competent oncology care to diverse participants, fostering a safe environment that respects and supports individual beliefs and needs. The Research Coordinator – RN maintains professional competence through ongoing development and practices in accordance with regulatory standards, ethical guidelines, and Nova Scotia Health policies.

Requirements

  • Degree or diploma in Nursing required
  • Current registration with NSCN required
  • Minimum of two years’ experience in nursing required
  • Current BLS-C required
  • Proficiency in MS Office (Word, Access, Excel, PowerPoint), email and internet
  • Demonstrated competencies in computer skills, including databases
  • Demonstrated clinical and assessment skills related to the scope required for this patient population (i.e. CPR, physical, mental and emotional assessment, phlebotomy , etc.)
  • Effective interpersonal, communication and teaching skills
  • Demonstrated time management and organizational skills
  • Effective research and analytical thinking skills
  • Strong negotiation, conflict resolution and rapport-building skills
  • Ability to work well independently as well as within a multi-disciplinary team environment

Nice To Haves

  • Oncology nursing experience an asset
  • Experience in clinical research an asset
  • CCRP (Certified Clinical Research Professional) or CCRA (Certified Clinical Research Associate) an asset
  • Transportation of Dangerous Goods certification an asset
  • Competencies in other languages an asset, French preferred

Responsibilities

  • Coordinates research projects within Nova Scotia Health.
  • Prescreens potential clinical trial participants.
  • Administers clinical trials.
  • Cares for participants (in the clinic setting, and on-call).
  • Manages study documents and data.
  • Provides clinical leadership and ensures ICH GCP compliant, appropriate, coordinated nursing care by the study team.
  • Delivers culturally competent oncology care to diverse participants, fostering a safe environment that respects and supports individual beliefs and needs.
  • Maintains professional competence through ongoing development and practices in accordance with regulatory standards, ethical guidelines, and Nova Scotia Health policies.

Benefits

  • health
  • dental
  • travel
  • long-term disability
  • life insurance coverage
  • defined benefit pension plan
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