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Clinical Research Nurse Manager CNM1 (Clinical Trials Unit) required for Radiation Oncology Unit Dublin

Clinical Research Nurse Manager CNM1 (Clinical Trials Unit) required for Radiation Oncology Unit Dublin

Nurse on CallDublin, IE
30+ days ago
Job description

Clinical Research Nurse Manager CNM1 (Clinical Trials Unit) required for Radiation Oncology Unit Dublin

  • Monday to Friday
  • Flexibility considered for right candidate
  • 6 month contract
  • Locatiosn Rathgar, Beaumont and St James

Duties

  • Screening potential trial patients; review of their medical history, histology, laboratory and radiology reports etc.
  • Participation in informed consent process. The CRN goes through in detail with the patient all aspects of participating in a trial, as going forward they are the patients contact.
  • Providing education, information and support for patients & their families
  • Maintaining trial related logs (screening, informed consent, patient ID logs etc)
  • Responsible for maintaining Investigator Site File
  • Involved in performing trial measurements for example toxicity assessments etc
  • Involved in the ongoing training of site staff, including Consultants, Registrars, Radiation Therapists, Nurses etc.
  • Involved in the designing and completion of patient pack, Case Report Forms (CRF)and all trial related documentation
  • Patient follow up. Where possible, for some Clinical Trials this is done by the CRN either by phone or in clinic.
  • Good Clinical Practice (GCP) training, is a mandatory requirement for all staff involved in clinical trials
  • Ensuring each protocol is in compliance with GCP (Good Clinical Practice
  • Registered Nurse with a minimum of two years post graduate experience
  • Experience working in the oncology setting
  • Ability to work on your own initiative and as part of a multi-disciplinary team.
  • Good communication and interpersonal skills
  • Good organisational skills and an ability to establish priorities
  • Versatility and ability to work to deadlines
  • Experience in co-ordinating clinical trials from initiation to closure would be advantageous
  • If any of the above are of interest to you;

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