**Job Description**
This PhD project aims to better understand the genetic and clinical variability of Inherited Retinal Diseases (IRDs), particularly those caused by mutations in the PRPH2 gene, which are a common cause of early vision loss. The project will involve studying a large patient cohort using detailed genetic analysis and advanced imaging techniques to identify genotype-phenotype correlations, characterize disease progression, and explore early disease changes. This crucial knowledge will improve prognosis, patient care guidance, and support the development of future gene-based therapies for PRPH2-IRD. The trajectory also includes close collaboration with the Center for Medical Genetics Ghent for functional research.
**Skills & Abilities**
• Keen interest in clinical research, ophthalmology, ocular genetics, and imaging techniques.
• Ability to work and communicate in a professional and correct manner with patients.
• Excellent English and Dutch communication skills, both spoken and written.
• Strong knowledge of French (recommended).
• Excellent analytical and problem-solving skills.
• Stress-resistant and flexible, with strong organizational skills.
• Highly motivated.
• Ability to function well independently as well as in a team.
• Ability to take initiative and have a hands-on mentality, perseverance, and critical mind.
**Qualifications**
Required Degree(s) in:
• Medicine
• Pharmaceutical Sciences
• Biomedical Sciences
• Related biological studies (Master’s degree required)
**Experience**
Other:
• 1 – 4 years of Research Experience in Biological sciences
• 1 – 4 years of Research Experience in Medical sciences
• 1 – 4 years of Research Experience in Pharmacological sciences
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