Organisation/Company University College Cork Department HR Research Research Field Medical sciences » Cancer research Researcher Profile Recognised Researcher (R2) Positions Research Support Positions Country Ireland Application Deadline 26 Sep 2025 - 12:00 (Europe/Dublin) Type of Contract Temporary Job Status Full-time Is the job funded through the EU Research Framework Programme? Not funded by a EU programme Is the Job related to staff position within a Research Infrastructure? No
Offer Description
Are you a qualified nurse, looking for an impactful role that involves helping patients whose lives have been impacted by cancer? Do you want to join a passionate and growing team with recent funding from the Breast Cancer Research Foundation to grow and find better diagnostics and treatments for patients with breast cancer?
The UCC Cancer Trials Group (UCC CTG) is looking for an enthusiastic research nurse (CNMII) to work in a growing team, supporting investigator-led research.
ABOUT UCC CTG:
* The UCC CTG is a new HRB funded collaborative team which aims to bring together a dedicated team of cancer specialists and research staff across the south of Ireland. The UCC CTG is part of Cancer Research @UCC, a translational cancer research centre within the College of Medicine & Health at University College Cork. The UCC CTG group includes 3 cancer trials units at Cork University Hospital (CTC @CUH), University Hospital Waterford and Bons Secours Hospital Cork.
* The role will be hosted in Cancer Research @UCC and the Cancer Trials Cork Unit at CUH (CTC @CUH) in the Breast Lung Gynaecology portfolio. The CUH unit has been in operation for close to two decades, serving a geographically diverse population of 1.2 million in the South of Ireland. This team has grown over the past few years and continued growth is projected for years to come. The CNMII will work closely under the guidance of Professor Roisin Connolly /CNM3 /Nurse Management and team members.
* Co-ordination of clinical and translational aspects of the project including direct interface with pathology department, scientific collaborators, external laboratories and data scientists etc.
* Clinical responsibilities.
* Working with pathology for slide cutting and storage, labelling etc
* Coordination of sample distribution to labs and payments/invoices for correlative studies.
* Collection of clinical data from relevant databases when required for abstract preparation
* Supporting team meetings (minutes/agendas/follow up tasks) specific to the project
* Support other studies taking place in the Cancer Trials Cork unit at Cork University Hospital where deemed necessary and in keeping with funding requirements
* Engage cross-functionally with different stakeholders, knowledge sharing, and building relationships.
* This role requires excellent communication and interpersonal skills, computer literacy, organization and an awareness of time management.
The MINA study – ‘Microbiome Immunotherapy Neoadjuvant Assessment’ - is a prospective observational study that aims to characterise and evaluate the bacterial population shown to be present in the immediate environment of breast tumours. Previous work has shown that these bacteria can alter the effectiveness of some commonly used anti-cancer drugs, and so it is hoped that data from this study can support the development of new biomarkers that can measure how well some patients might respond to chemotherapy compared to others.
EXPERIENCE REQUIRED:
* Qualified Nurse (Mandatory RGN, BSc).
* Oncology background or related experience would be a strong advantage.
* Strong interest in gaining experience in this area will also be considered without previous experience in Oncology nursing.
* To undertake research, working under the direction of a Principal Investigator or their nominee in clinical areas to support the research project/area. Demonstrate accountability and responsibility for professional practice within a research nurse capacity.
* Provide a high standard of clinical research work within a multi-professional research team.
* Ensure clinical research work is conducted in accordance with clinical research protocols and in accordance with good clinical practice
* To regularly assess the needs of the research project/area and effect any changes as required.
* To participate in internal and external working groups to develop and share evidence based best practice.
RESEARCH
* Manage, coordinate, organize and implement basic science and clinical trial protocols to support the research project/area.
* To ensure accurate collection and maintenance of all study records, including those of team members in line with best practice, ICH-GCP.
* To actively participate in recruiting patients for trials, liaising with other professional groups and research staff to achieve this as required.
* When appropriate, assist in the development of Standard Operating Procedures (SOPs) to support the research project/area.
* Facilitate effective communication of complex study information with all relevant research personnel, including medical, nursing, administrative and pharmacy staff, as required.
* Ensure patients are fully informed of clinical trial/research study details prior to their enrolment
* To ensure patient confidentiality and dignity is upheld at all times.
MANAGEMENT
* Manage own workload, patient interviews and co-coordinating investigations and procedures and arranging any follow up necessary for complex research trials, as required.
* Ensure that clinical research activity is undertaken to a high standard and in line with Good Clinical Practice Guidelines and regulatory requirements.
* Work collaboratively and innovatively within the organisational research infrastructure.
* Liaise effectively with sponsor representatives, CRO representatives and associate ancillary staff and external vendors in trial set up, conduct and close out.
* Compile information for and accurately complete project reports for delegated studies.
* Contribute to clinical documents (protocols, IBs, Study Manuals, CRF completion guidelines, SOPs, monitoring plans, etc.), project reviews.
* Coordinate team meetings and ensures good communication within the project team.
* Develop effective working partnership with staff, ensuring the two-way flow of all necessary documentation and information.
* Report adverse events to Principal Investigator or his/her nominee and ensure completion of appropriate documentation.
* Inform the Principal Investigator or his/her nominee of any untoward incidents or problem areas affecting the research project/area.
* Compile information for and accurately complete project reports for delegated studies.
* Ensure prompt management of study related correspondence.
* Promote effective teamwork, initiate and support management of change within the research project/area, as required.
* Ensure safe use of equipment in the research area.
EDUCATION & DEVELOPMENT
* Participate in teaching programmes for staff as required.
* Act as role model, encouraging staff to develop new ways of working.
* Assist/educate participants in research protocols and methodologies.
* Recognise and use spontaneous and formal learning opportunities and share knowledge and experience with other staff.
* Continue to maintain and develop personal and management skills by undertaking mandatory and other training as required.
* Support research staff in the implementation and organisation of basic science and clinical trial protocols when appropriate.
SPECIFIC REQUIREMENTS
The successful candidate will be expected to have:
ESSENTIAL
* A graduate qualification in a field or discipline relevant to the area of investigation i.e. BSc, MSc or PhD, RGN. (Nurse qualification is mandatory for this post)
* Be a registered nurse with the Nursing and Midwifery Board of Ireland (or entitled to be registered)
* Evidence of ongoing professional development.
* Clinical research experience/interest in clinical research.
* Excellent verbal and written communication skills.
DESIRABLE
* Experience working with biospecimen collection, biobanks, laboratory teams to support the research protocols.
* Demonstrable knowledge of good clinical practice.
* Experience in Clinical or Translational research coordination
* Ability to work independently or as part of a team.
* Able to use initiative.
* Able to prioritise and deliver agreed objectives.
* Strong communication and influencing skills
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