:One of the leading Pediatric / Children's hospitals is currently looking for aGenomic Scientist for the UAE location who will analyze clinical genomic data and assess the biological impact of genomic variants, focusing on their association with constitutional genetic disorders in a pediatric diagnostic setting. Working within a highly skilled team of molecular technologists, bioinformaticians, genetic counselors, and a Laboratory Director, this role reports directly to the Laboratory Director, Genomics.Core Responsibilities:Genomic Data Analysis:

• Analyze chromosome microarray results and NGS-based tests (e.g., targeted panel, whole exome sequencing).

• Assess data quality using methods like Sanger sequencing and bioinformatics workflows.

Variant Curation:

• Conduct detailed literature reviews for variant and gene classification.

• Maintain internal genetic variant databases and adhere to ACMG guidelines.

Diagnostics and Reporting:

• Draft diagnostic reports and support assay validations.

• Create technical documentation and participate in quality improvement initiatives.

Research & Development:

• Engage in clinical research and assist with new assay validation.

• Contribute to professional practice development and support staff training.

Professional Development:

• Maintain technical expertise through self-learning and reflective practice.

• Act as a mentor for new staff and participate in quality initiatives.

Collaboration and Communication:

• Collaborate with a multidisciplinary team to ensure precise diagnostics and patient care.

• Foster teamwork, engage families in patient care decisions, and provide clear communication to support informed choices.

Safety and Compliance:

• Advocate for child safety, report risks, and uphold a culture of safety.

• Actively participate in safeguarding strategies and risk mitigation.

This role requires a strong technical background in genomic diagnostics, effective teamwork, attention to detail, and a commitment to delivering high-quality, patient-centered care in a pediatric setting.RequirementsEducation & Experienceo MS or PhD in molecular biology, biochemistry, human genetics or related scientific fieldo In-depth understanding of the genetic basis of hereditary disorderso Work experience with commonly used public genomics datasets (1000 genomes, ExAC,gnomAD, OMIM, ClinVar, PharmGKB etc.)o Knowledge of literature curation methodologieso Preferred: Previous laboratory or research experience in a disease area, genetic pathway orgenomic testing technologyo Understanding of bioinformatics tools and workflows used to identify genomic variants from next-generation sequencing datao Prior experience working in a clinical diagnostic environment is a plusCertification and Licensureo Ability to qualify for UAE allied healthcare personnel licensure requirementso Life Support and Advanced Life support Trainingo American Heart Association (AHA) Basic Life Support (BLS) required OR Intermediate LifeSupport (ILS)o Positive, enthusiastic and motivated individualo Effective communication and interpersonal skillso Team playero Experience documenting in an electronic medical record an asseto Proficiency with Microsoft Office Suiteo Ability to speak and write English is requiredo Arabic language skills (spoken) an asseto International English Language Test System (IELTS) xe2x80x93 a minimum score of 6.0 or equivalent.The English Proficiency evidence must be valid and not exceed 2 years.WORK LOCATION - DUBAI, UAE.Follow theTo view other vacancies we have, please check our website ( ) and follow us on our social media accounts - / / /Disclaimer: Black Pearl will never ask for money or any form of charge our candidates just to process or consider their application for any of our available vacancies. If you happen to receive such a request from any members of our staff or other individuals claiming to be part of Black Pearl, please do call our office at +9712 622 55 03 or drop us a message on our website - .

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