Post-Doctoral Research Associate in Cancer Genomics (Cancer Genomics)
Контакты
Формат работы
onsite
Тип работы
fulltime
Английский
b2
Страна
UK
bioinformaticscancer genomicsgenetic epidemiologyplinkprostate cancerpolygenic risk scoresgenomic data analysisgenotype quality control
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Хорошая вакансия
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Роль четко описана и связана с профильными исследованиями в известном университете, но зарплата не указана, а для работы требуется право на трудоустройство в Великобритании без спонсорства визы.
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Без спонсорства визыЗарплата не указанаЧеткие задачиСовременные инструментыЗначимые исследования
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Post-Doctoral Research Associate in Cancer Genomics (Cancer Genomics): Analysing genomic data and calculating prostate cancer polygenic risk scores for the GP-TEST-Pro clinical study with an accent on genotype quality control, ancestry assessment, and variant harmonisation. Focus on validating a 451-SNV risk score, evaluating genomic markers for clinically significant prostate cancer detection, and integrating rigorous genetic epidemiology methods.
Location: Oxford Road, Manchester, United Kingdom. Applicants must demonstrate the right to work in the UK; this role is not eligible for Skilled Worker visa sponsorship.
Company
hirify.global research role contributing to the multidisciplinary GP-TEST-Pro prostate cancer clinical study.
What you will do
Receive, securely store, and manage genomic data according to University, NHS, and study governance requirements.
Perform genotype and imputed-data quality control, including sample- and variant-level checks, ancestry assessment, allele harmonisation, and preparation of analysis-ready datasets.
Use genetic analysis tools such as PLINK/PLINK2 and imputation server outputs to process and analyse genomic data.
Calculate and validate a 451-SNV prostate cancer polygenic risk score using published effect sizes.
Evaluate additional genomic markers and polygenic risk score approaches relevant to clinically significant prostate cancer detection.
Requirements
PhD, or imminent PhD completion, in genetic epidemiology, statistical genetics, bioinformatics, cancer genomics, epidemiology, data science, or a related quantitative discipline.
Hands-on experience conducting cancer genomic medicine research and analysing genetic or genomic datasets.
Experience cleaning, quality-controlling, and managing genotype or imputed genomic data, including pre- and post-imputation checks.
Experience calculating, validating, or applying polygenic risk scores with variant effect sizes and ancestry or population-structure adjustment.
Understanding of SNVs, alleles, imputation, linkage disequilibrium, ancestry, population structure, and principal components.
Right to work in the UK required; Skilled Worker visa sponsorship is not available.
Nice to have
First- or co-author publications in cancer detection research.
Experience with prostate cancer genetics, cancer risk prediction, diagnostic accuracy, calibration, discrimination, or multivariable risk modelling.
Experience integrating genomic data with clinical, epidemiological, biomarker, or imaging data.
Experience working with PPI groups and co-investigators.
Expertise in cancer screening or early detection research.
Culture & Benefits
Collaborative, multidisciplinary, inclusive research environment.
Generous employer pension contribution.
29 days of annual leave plus bank holidays and Christmas closure.
Ride-to-work and electric vehicle car schemes.
Flexible and hybrid working information is available, subject to the role's requirements.
Hiring process
Applications close at midnight on the stated closing date.
Shortlisting and interviews are handled by the role's academic contact.
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