Jobs

Closing Date: 30/01/2022

Location: Wellington, New Zealand

Location: Wellington Hospital, New Zealand

Contract: Permanent and fixed-term, full-time and part-time. Monday - Friday (up to 40 hours per week, including flexible working hours) 

Salary: PSA Allied Health Technical and Scientific (Salary Scales as stated on section 5.8.17 - see link below)

About the role

An exciting opportunity exists for experienced, professional and highly motivated genetic scientists to join our progressive laboratory.   Wellington Regional Genetics Laboratory (www.wellingtongenetics.co.nz) is a busy diagnostic laboratory providing an extensive range of genetic tests and has established links to other services; to ensure a high standard of service.   Key service prioritises include the application of next generation sequencing technologies, expansion of our molecular oncology service and supporting the increased workload across all areas of the laboratory. 

We invite applications from diagnostic genetic scientists with experience in a clinical diagnostic laboratory.  You must be a NZ registered Medical Laboratory Scientist or eligible for registration (www.mscouncil.org.nz). Starting salary will be dependent on your level of experience and qualifications. The positions are permanent and both full-time and part-time options will be considered. 

We are also willing consider a minimum twelve month fixed term posts for suitable candidates who are unsure about permanent relocation. 

Wellington is the capital city of New Zealand, set among green hills surrounding a majestic harbour.  It has a well-established reputation as a vibrant arts and entertainment centre of NZ.  Wellington offers genuine work/life balance. For further information on Wellington please visit https://www.wellingtonnz.com/ 

If you see your future in our team, please feel free to contact us to discuss further.

About our team

Wellington Regional Genetics Laboratory (WRGL), a team of 25 staff (administrators, technicians and scientists),  is an integrated cytogenetic and molecular genetic service; karyotype, FISH, microarrays and DNA testing of prenatal, postnatal and malignancy samples (www.wellingtongenetics.co.nz).

Our aim is to ensure operations, products, advice and services meet the requirements of both internal and external clients thereby providing a timely, appropriate and high quality clinical laboratory service. This laboratory complies with or exceeds all accepted standards as embodied in IANZ Registration Criteria and the International Standard NZS/ISO 15189:2012.

About you:

• Team player 
• Excellent communication and scientific skills 
• Experience in diagnostic Genetics 

About us

Here at the 2DHBs (Capital & Coast District Health Board and Hutt Valley District Health Boards) we embrace diversity and welcome applications from all people, including all gender identities, ages, ethnicities, sexual orientations, disability and religions. A workforce that is diverse and inclusive means that we are better positioned to understand and serve our community.

The 2DHBs are pro-equity health organisation, with a particular focus on Māori, Pacific Peoples, and the Disability Community.

To find out more about us click on the following links:

Capital and Coast DHB

Hutt Valley DHB

Mental Health, Addiction and Intellectual Disability Service

PSA Allied Health Technical and Scientific MECA (for Salary Scales)

How to apply

Click the apply now button to send your application directly to us. For further information on this role please email Philip.Adamson@ccdhb.org.nz and indicate the job title and vacancy number (AH301-21) in the subject line.

Please note we will be reviewing applications when received and will progress through the recruitment process until advertising closes on 30 January 2022.

For further information please contact:

Philip Adamson
Email: Philip.Adamson@ccdhb.org.nz

Recruitment, Level 11, GNB, Wellington Hospital, Riddiford Street
Wellington
New Zealand
6021

Closing Date: 07/02/2022

Location: Remote

For further information please contact:

Samantha Barber
Email: samantha.barber@genepeople.org.uk
Website: www.genepeople.org.uk

PO Box 3378,
South Croydon

CR2 IPR

Closing Date: 30/01/2022

Location: Salisbury

An exciting opportunity has arisen at the Wessex Regional Genetics Laboratory (WRGL) in Salisbury, to join our dynamic team of genomic scientists. This is a permanent full time post for a new role as Band 8a HCPC registered Principal Clinical Scientist in Cancer Genomics in an expanding team. We are seeking an experienced and dynamic individual for the position of Principal Clinical Scientist within the Haemato-oncology team. The analytical portfolio of the section comprises a wide range of genomic techniques, including G-banding, FISH, next generation sequencing (NGS) panels and whole genome sequencing, and will shortly include SNP array. The post holder will be highly involved in the day-to-day running of the laboratory and will be required to analyse, interpret and authorise complex clinical reports for a wide range of haematological disorders and some solid tumours. The role requires the highest quality of attention to detail, to ensure that patient results are delivered in a safe and efficient way in order to direct patient management and therapeutic decisions. In addition, the post holder will provide specialist advice and support to users of the Department service, particularly in the context of multidisciplinary teams and genomic tumour advisory boards. The role is multi-disciplinary with cross-over between cytogenetics and molecular genetics. Further details and applications via NHS Jobs Ref : 269-SFT6484

For further information please contact:

Laura Chiecchio
Email: l.chiecchio@nhs.net

Wessex Regional Genetics Laboratory,
Salisbury
Wilts
SP2 8BJ

Closing Date: 30/01/2022

Location: Sheffield

We are looking to recruit to the post of Clinical Scientist Service Lead for the Core Rare Disease Service, based at Sheffield, with agile working options and potentially with some travel across the GLH geography. The post will form part of the GLH laboratory team and, together with the Lead Scientists and their deputies, ensure that NEY GLH is at the forefront of National Genomic Medicine Service. This will include: • Leading a group of scientific staff to deliver timely, high-quality genomic services in Core Rare Disease. • Developing your specialist knowledge and expertise, across genomic technologies. • Working with clinicians and other laboratories at local, regional and national levels on behalf of the GLH, and facilitating multidisciplinary meetings. • Driving service development. • Undertaking research and innovation activity. The post provides the opportunity to join a collaboration at the forefront of transforming and shaping genomics services for the future. If you like what you have read and would like to join us on our exciting journey, then we would welcome your interest and application. For a confidential discussion please contact Richard Kirk (richard.kirk2@nhs.net, 07785 655 461). To apply, go to http://www.healthjobsuk.com/vacancy/3751619

For further information please contact:

Richard
Email: Kirk

Closing Date: 30/01/2022

Location: Bristol

http://jobs.nbt.nhs.uk/job/v3765996 Consultant Clinical Scientist in Cancer Genomics (band 8C) Bristol Genetics Laboratory, South West Genomics Laboratory Hub A vacancy has arisen within the South West Genomics Laboratory Hub at Bristol for a Consultant Clinical Scientist in the Solid Tumour team. This is a new post due to service expansion. In this vital role, you will act in a Consultant Clinical Scientist capacity for the Solid Tumour services for the South West Genomic Laboratory Hub. The post holder will maintain overall leadership the Solid Tumour section of the Cancer Genomics team, developing services for their sub-specialty in line with the requirements of the SWGLH and NHSE National Genomics Test Directory. The post holder will provide Consultant level clinical advice, clinical liaison and strategic direction for their area of service and will also deputise for the lead Consultant in Cancer for aspects of Cancer service strategy and management. The post holder will also lead on specific projects. As a member of senior leadership team the post holder will also contribute to strategic direction of BGL and the SWGLH Cancer Genomics services under the overall direction of the Head of Cancer Genomics and the Head of Department. Possession of FRCPath is essential, as is significant experience in cancer genomics, in particular solid tumour, services. The successful candidates will be expected to work 37½ hours per week full-time over 7 days a week, including participation in regular weekend and out of hours working. Services are currently configured to enable a combination of remote working as well as working on site. Part time working will be considered.

For further information please contact:

Chris Wragg
Email: christopher.wragg@nbt.nhs.uk
Website: http://jobs.nbt.nhs.uk/job/v3765996

South West Genomic Laboratory Hub, Bristol Genetics Laboratory
Bristol

BS10 5NB

Closing Date: 27/02/2022

Location: London

Band 7 Clinical Scientist HCPC Registered Clinical Scientist /Pre-Registration Clinical Scientist (Cytogenetics) – Band 7 (37.5 hour per week - Substantive) Applications are invited from State Registered Clinical Scientists / Pre-Registration Clinical Scientists in Genetics to join the SIHMDS Laboratory within North West London Pathology at Hammersmith Hospital, hosted by Imperial NHS Trust. We are seeking an enthusiastic, self-motivated Clinical Scientist with proven extensive experience of Cancer Cytogenetics to work in the cytogenetics section of our laboratory and contribute to the provision of a timely and efficient ISO15189 accredited service. Applicants should ideally hold HCPC registration as a Clinical Scientist and be highly competent with bone marrow karyotyping and FISH analysis. The post holder will have responsibility for managing the technical team ensuring smooth running and quality management of the wet laboratory. Good communication, team working, and supervisory skills are essential to guide and manage the junior technical staff. They will also be required to take responsibility for delivering a high-quality routine laboratory diagnostic service for a range of specialised cytogenetic and molecular investigations including analysis, result evaluation, interpretation and reporting of haematological malignancies in a clinical setting. International or UK applicants without HCPC registration but with an extensive experience of bone marrow karyotyping and FISH analysis, including high level interpretation and report writing skills will also be considered. These applicants would be expected to already have a complete portfolio or equivalent experience to be eligible to apply for HCPC registration as a Clinical Scientist. Only applicants who meet the experience criteria will be interviewed and will be appointed at band 6 level until the registration is achieved. Experience with FFPE-FISH analysis and molecular analysis including next generation sequencing and whole genome sequencing would be an added advantage. Suitable international applicants can be provided with sponsorship on the new skilled worker visa (SOC code-2112 - Cytogeneticist) This role is substantially laboratory based, but some flexibility / ad-hoc remote working options can be considered. Please note that if there are enough eligible applicants for this post, this advert may close early. The Trust reserves the right to close this vacancy early should we receive 50 applications prior to the advertised closing date. Please ensure you submit your application as soon as possible. We are committed to equal opportunities and improving the working lives of our staff and will aim to consider applications to work flexibly, part-time or job share. Please talk to us at interview about the flexibility you may need. Apply through : http://jobs.imperial.nhs.uk/job/v3830266 Further details / informal visits contact Cytogenetics Head: Dr Udayakumar Achandira, on 02033131503 or udayakumar.achandira@nhs.net

For further information please contact:

Dr Udayakumar Achandira
Email: udayakumar.achandira@nhs.net

Hammersmith Hospital, Du Cane Road W12 0HS
London
UK
W12 0HS

Closing Date: 21/02/2022

Location: Auckland

One of New Zealand’s largest and most highly regarded health providers are looking for two passionate Genetic Counsellors/ Associate Genetic Counsellors! Excellent opportunity to join Te Puriri o Te Ora (Regional Cancer and Blood Services) Relocation assistance provided, if needed One 12 months fixed term, full time role and one permanent, full time role based in Auckland, New Zealand Genetic Health Service NZ – (Northern Hub) is one of the three hubs of the New Zealand National Genetic Service. The Northern Hub covers the population in the upper North Island. The service is based at Auckland City Hospital, New Zealand and has a core team of 5 Geneticists and 8 Genetic Counsellors. The service provides prenatal, general and cancer genetic counselling care through education, information and support to individuals, families/Whānau and other agencies. We are seeking two enthusiastic Genetic Counsellors/Associate Genetic Counsellors for a full time, fixed term position (40 hours per week) covering a parental leave and a full time, permanent position. As part of our multidisciplinary team you'll manage a caseload of general and cancer cases. Excellent written, oral and interpersonal communication skills are essential. You will be responsible for providing coordinated, efficient and quality genetic counselling service to patients and family/ Whānau. Some key accountabilities, dependant on experience, include: Determine the patients understanding of referral and give information on genetic mechanisms Record family pedigrees clearly and legibly. Participate in intake phone calls with patients Gather clinical information, family consent and laboratory information as required by Geneticists and Senior Genetic Counsellors. Accurately elicit the questions/advice by the patient and by the referrer. Accurately prepare clinical letters, documenting issues, outcomes and recommendations arising from the consultation. Ability to refer to other specialties where needed. Obtain documentation to confirm family history or diagnosis details where necessary. Obtain informed consent for genetic testing/release of information to ensure patients and/or family agree with proposed management where necessary To be considered for this role, the ideal applicant must have the following: Master in Genetic Counselling Have your FHGSA or MHGSA or Australian Society of Genetic Counsellors Board eligible In addition to the opportunity to work in a large, modern comprehensive facility, Auckland City Hospital is the largest in New Zealand. It has a vibrant mixture of lifestyles and cultures and offers easy access to stunning and diverse scenery and a wonderful range of outdoor pursuits. With its beautiful countryside and dynamic metropolitan centres, New Zealand offers a lifestyle suitable for all. This is a great opportunity for you to come and experience the kiwi lifestyle and hospitality, whether that be living permanently or coming for an extended ‘visit’. We would love to hear from you to discuss this opportunity with you. To apply to this opportunity, please visit our careers site www.careers.adhb.govt.nz or click on the link below to submit an application attaching your CV and covering letter. For further information, please contact Kimberly Gamet, Team Leader and Senior Genetic Counsellor at kimberleyg@adhb.govt.nz For assistance with your application, please contact Caryne Tee, Recruitment Consultant on CaryneT@adhb.govt.nz Auckland DHB is committed to the application of the Vulnerable Children Act 2014 and its intent to improve the safety of all children. This position is a Children’s Worker role as defined by the Act. For the biggest health sector job board in New Zealand visit kiwihealthjobs.com

For further information please contact:

Kelsey Deere
Email: kelseydeere@neonlogicagency.com
Website: https://careers.adhb.govt.nz/health-careers-job-search/details/AUC13963?utm_source=Job+Board&utm_medium=BSGM&utm_campaign=Genetic+Associate+-+Cancer+and+Blood+Services%2C+Auckland+City+Hospital

PO Box 13265,
Tauranga
Bay of Plenty
3141

Closing Date: 28/02/2022

Location: Lausanne, Switzerland

The Lausanne University Hospital (CHUV) invites application for the 80-100% position of: Clinical Laboratory Geneticist (onco-haematology) The Oncogenomic Haematology Laboratory holds full accreditation to ISO 15189 standards and is the largest cancer genomic laboratory in Switzerland, dedicated to comprehensive diagnostic analysis comprising of cyto- and molecular genomics in hematological neoplasia. As a Swiss reference center, it provides diagnostic services at the regional level within the Canton de Vaud and nationally throughout Switzerland. The molecular genomics unit provides hereditary and somatic genetic diagnostic services using state of the art technologies including next generation sequencing and digital PCR. Context The Lausanne University Hospital (CHUV) is one of the 5 Swiss University Hospitals. Thanks to its collaboration with the Faculty of biology and medicine of the University of Lausanne and the EPFL, the CHUV plays a leading role in the domains of the medical care, the medical research and the training. Mission Provide molecular and or cytogenomic diagnostic services to the referring clinicians (haematologists, oncologists, paediatricians and geneticists) and work in close collaboration with the team of clinical laboratory geneticists and genetic technologists. Ensure internal and external quality controls in agreement with the accreditation requirements Develop, implement and update state-of-the-art molecular approaches You become an expert in your field and are willing to write/publish the scientific reports, participate in international meetings and present scientific data Profile The successful applicant must be board certified in medical genetics. The position requires familiarity with reporting guidelines for both somatic and germline genetics in a diagnostic genetic setting and significant experience with interpreting and reporting genetic alterations identified with cytogenomics and or molecular genetic testing strategies. Experience in bioinformatics and genomic analyses (such as NGS, karyotyping, FISH and/or SNP array) in hematological malignancies would be advantageous. He/she will be expected to interact closely with clinical and/or research faculty members and should possess excellent communication, analytical and organizational skills: both written and verbal and have a good working knowledge in French or the capacity to acquire it quickly. We offer Becoming an employee of the Lausanne University Hospital at the canton of Vaud is the assurance of: First-rate social benefits Annual salary according to Canton VAUD scales level 9 to 12 based on experience 25 days vacation per year Stimulating work environment that inspires excellence Contact and application For further information, please contact the head of the oncogenomic haematology laboratory Prof. Jacqueline Schoumans phone +41 21 314 33 87 or +41 79 556 85 56. Application including a full curriculum vitae, reference letters and copy of diplomas can be sent until 28.02.2022 to: Jacqueline.Schoumans@chuv.ch.

For further information please contact:

Prof. Jacqueline Schoumans
Email: Jacqueline.Schoumans@chuv.ch
Website: www.chuv.ch/fr/log/accueil

Service d’hématologie, Laboratoire d’oncogénomique, Réception des laboratoires BH18-100
Lausanne
Vaud
1011