Clinical Data Scientist
Confirmed on the employer's own hiring board on Nov 10, 2026. First seen by Alion on Nov 10, 2026.
Join Cyllene Therapeutics as a Clinical Data Scientist, where you will play a crucial role in overseeing clinical study data throughout the lifecycle of our clinical trials. You will work closely with Clinical Development and our external statistical and data management vendor to develop and implement a clinical intelligence framework for monitoring incoming blinded clinical data. The ideal candidate will have a strong foundation in clinical data management, an understanding of clinical research and statistical data analysis, and a keen interest in artificial intelligence.
Missions
- Develop and implement approaches for data oversight and monitoring incoming blinded clinical study data, generating meaningful clinical intelligence outputs.
- Collaborate with the external data management and statistical vendor to understand data flows, data structures, and study-specific requirements, and support data review processes.
- Work with clinical study databases and other relevant data sources to integrate and analyze clinical trial data, developing repeatable analytical workflows for ongoing data surveillance.
Profil recherché
**Education:** Bachelor’s or Master’s degree in Biostatistics, Data Science, Biomedical Informatics, or a related field.**Professional experience:**
* At least 5 years of relevant experience working as clinical Data manager in a CRO or Biotech or Pharmaceutical company or closely related function.
* Strong understanding of clinical trial data and clinical research concepts.
* Hands-on experience working with clinical study databases and clinical data management systems.
* Strong knowledge and experience in AI usage in Data analysis/Clinical Intelligence
* Experience reviewing and assessing clinical data for quality, completeness, consistency, and trends.
* Strong analytical and problem-solving skills with the ability to identify meaningful patterns in complex datasets.
* Working knowledge of statistical concepts and data analysis.
* Experience working with external clinical data management, statistical, or CRO vendors.
* Experience working in a blinded clinical trial environment.
* Strong proficiency with SQL and/or analytical programming languages such as Python or R.
* Experience with data visualization and reporting tools.
* Experience in data management of clinical trials in neurology or neurology-urology indications preferred.
* Ability to translate analytical findings into actionable information.
**Soft skills:**
* Analytical Thinking & Scientific Curiosity
* Proactivity & Problem-Solving
* Cross-functional Collaboration & Communication
* Autonomy & Adaptability
**Languages:** English (spoken and written)
*Cyllene Therapeutics is an equal opportunity employer. We welcome applicants of all backgrounds and do not discriminate on the basis of race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status or any other protected characteristic.*