عالم باحث مساعد في المعلوماتية الحيوية

The Staff Scientist - Assistant Level (Bioinformatics) supports research within the specific areas of research programs and performs a variety of procedures using established methods and techniques. The incumbent conducts moderately complex experiments, critically evaluates scientific literature and findings, performs experiments and interprets data.

Responsibilities

• Under the general supervision of more senior scientific staff performs research tasks of a moderate scope.
• Performs scientific research at the highest standards.
• Conducts experiments, analyzes and processes data.
• Collects and summarizes scientific data/ information for experiments and archiving.
• Keeps accurate records of experiments, checks data and informs discrepancies.
• Assists with evaluating and testing new processes.
• Complies with safety regulations/ standard protocols.
• Collaborates with other Sidra members to apply the results of research and/or develop new techniques or practices.
• Prepares research results for journals and report publications.
• Presents ongoing work and findings to colleagues both local and in academic conferences.
• Communicates results/findings to the relevant scientific community via published papers.
• Develops and applies novel research methodology to investigate and perform feature extraction in medical imaging, molecular and clinical data for predicting patient outcomes that will be translated into patient care.
• Builds innovative artificial intelligence (AI) solutions using latest and advanced algorithms for improved patient care.
• Implements methods and algorithms for analysis of complex multi-omics data sets including whole exome sequencing (WES), whole genome sequencing (WGS), targeted capture sequencing, RNA-seq, single-cell RNA–seq, ChIP-seq, Methylation sequencing, miRNA-seq, metabolomic and proteomic data.
• Makes use of publicly available biological data including TCGA, GEO, TCIA, cbioportal etc.
• Analyzes rare genetic variant for familial diseases to identify pathogenic variants of likely therapeutic intervention.
• Writes progress reports and research grant proposals for funding agencies.
• Adheres to Sidra’s standards as they appear in the Code of Conduct and Conflict of Interest policies.
• Adheres to and promotes Sidra’s Values.

In view of the evolving needs and opportunities within Sidra, this position may be required to perform other duties as assigned and reporting relationships may vary.

Qualifications

ESSENTIAL

PREFERRED

Education

PhD in Bioinformatics

Experience

Successful completion of Post-Doc fellowship

Job Specific Skills and Abilities

Knowledge of scientific research methods and evaluation of research results

Effective problem solving and analytical skills and ability to be detail oriented

Strong background in multi-omics data analysis, including WES, WGS, RNA-seq, single-cell RNA-seq, ChIP-seq, and proteomics.

Experience handling and analyzing large-scale biological datasets from public repositories (e.g., TCGA, GEO, TCIA, cBioPortal).

Competence in statistical analysis and data visualization using programming languages such as Python and R.

Familiarity with artificial intelligence (AI) and machine learning methods for clinical prediction and data integration.

Ability to develop and implement novel algorithms and pipelines for feature extraction and predictive modeling in medical imaging and multi-modal clinical data.

Prior experience in rare disease genetics and identification of pathogenic variants in familial cohorts.

Strong publication record or demonstrable ability to draft manuscripts for peer-reviewed scientific journals.

Strong knowledge of statistical methods and tools

Ability to assist in the management of a project, overcome obstacles, and meet deliverable deadlines

Proficiency with Microsoft Office suite

Fluency in written and spoken English

Experience in one or more of the following disease areas: nephrology (e.g., congenital or genetic kidney disorders), cardiovascular disease (e.g., inherited or structural heart conditions), neurological disorders (e.g., developmental or degenerative syndromes), and congenital malformations. Prior work may include disease modelling, biomarker discovery, genomic characterization, or translational research aimed at understanding pathophysiology and improving clinical outcomes.