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Clinical Research Nurse Manager CNM1

1 month ago

Dublin, Ireland TN Ireland Full time

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

Client: Nurse on Call

Location: Dublin, Ireland

Job Category: Other

EU work permit required: Yes

Job Reference: 595997fb0eb1

Job Views: 147

Posted: 21.01.2025

Expiry Date: 07.03.2025

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
  • Locations: 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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