Perinatal Genetics and Genomics Fellow 261020

The National Maternity Hospital; Dublin; On-site; EUR 60,000 - 70,000; Full time

Job summary

The National Maternity Hospital invites applications for a 1-year, full-time Fellow in Perinatal Genetics and Genomics. Based at NMH, the post reports to the Head of the Prenatal Clinical Genetics and Genomics department.

The ideal candidate will hold a Medical degree and be completing training in Obstetrics and Gynaecology or Clinical Genetics. An interest in genetics is desirable, with opportunities to contribute to teaching and research.

Qualifications

• Medical degree required; training in Obstetrics and Gynecology or Clinical Genetics ongoing.
• Interest in genetics desirable.
• Experience with MDTs and liaising with laboratories internationally is helpful.

Responsibilities

• Communicate with patients and families attending the service in person, by phone or virtually.
• Contribute to clinics with the consultant geneticist and obstetricians in fetal medicine, maternal medicine and recurrent miscarriage.
• Coordinate with colleagues in the Prenatal Genetics team and laboratories regionally and internationally.
• Help with teaching and education: present findings, contribute to publications, and assist in genetics teaching.

Skills

Phlebotomy

Communication

MDT collaboration

Excel

Education

Medical degree

Tools

Excel

Job description

Fellow in Perinatal Genetics and Genomics

The National Maternity Hospital (NMH) is seeking applications from suitability qualified persons for the post of Fellow in Perinatal Genetics and Genomics. This is a 1-year full time fellow post based at the NMH. This role will report to the Head of department, Prenatal Clinical Genetics and Genomics.

The ideal candidate will hold a Medical degree and will be completing training in Obstetrics and Gynaecology or Clinical genetics. An interest in genetics is desirable.

Skills and Abilities

phlebotomy, good communication skills, ability to work as part of an MDT and liaise with stakeholders in laboratories internationally with consultant support, competent with Excel,

Desirable

ability to develop teaching material for SpR colleagues and other medical staff, to develop the database with support.

Knowledge

basic knowledge of genetics and be willing to engage in structured teaching to learn more knowledge of MDT working including with Fetal medicine, recurrent miscarriage and neonatology.

Responsibilities & Accountabilities (in no particular order of priority)

• Communicate with patients and families attending the service (face-to-face, phone, virtual platforms)
• Clinical: contribute to clinics including joint clinics with the consultant geneticist as well as with obstetricians in areas including fetal medicine, maternal medicine, recurrent miscarriage etc. Manage a clinical caseload.
• Communicate with colleagues in the Prenatal Genetics team and broader professional community: laboratory colleagues, regionally and internationally, along with other specialties at The National Maternity Hospital and all regions covered by the service.
• Educational Activities: Present findings of research, audit and clinical practice to large groups of staff or members of the public. Participate in writing for publication in medical/counselling/lay journals. Participate in the teaching of genetics to medical personnel, other health care professionals and members of the public.
• Prepare and present scientific articles in clinical and departmental journal clubs. Act as an educational resource for medical and other personnel attached to the clinical genetics team including student and trainee genetic counsellors. However, the individual will not be the named mentor/supervisor of junior colleagues.
• Work on the genetics department database and prepare cases for publication under the supervision of the clinical lead.
• Co-ordinate complex genetic testing in pregnancy including both known diagnoses and unknown diagnoses, under the supervision of the Clinical geneticist.
• To co-ordinate care of genetics patients attending NMH form other hospitals
• To co-ordinate samples and liaise with the relevant laboratories
• To competently complete genomic test requests and co-ordinate the testing process
• To complete letters to patients and other HCP's which will be co-signed with the clinical geneticist
• To follow-up on cases and ensure testing is completed in a timely manner
• To contribute to development of the department through education and learning activities, database management and publications.
• To collaborate the deep phenotyping clinics with Fetal medicine and take part in those.
• To work with the fetal medicine team to organise interventions and scans for genetics patients.

Flexibility

This post requires a high level of flexibility to ensure the delivery of an effective and efficient service. Therefore, the post holder will be required to demonstrate flexibility on occasion as and when required by their manager.

Please note

This post will be offered as an Holles 2000 contract and remunerated at Pt 1 of the Registrar scale of the HSE as at June 2026.