Social network you want to login/join with:
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;
#J-18808-Ljbffr