Data Analyst
at AliveDx
Penicuik EH26 0BF, , United Kingdom -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 19 Jan, 2025 | Not Specified | 19 Oct, 2024 | N/A | Statistical Packages | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
At AliveDx, we empower diagnostic insights, transform patient care, and innovate for life. With over 30-years in in vitro diagnostics, we put the health of patients first by creating innovative solutions designed for faster diagnostic results. Alba, our blood bank reagents portfolio and MosaiQ®, one of the first multiplexing and multimodality automated testing platforms, are designed to make labs more efficient and clinical decision-making more effective. Our journey started as Alba Bioscience, and later, Quotient. Today, as AliveDx, we innovate for life.
QUALIFICATIONS & EXPERIENCE REQUIRED
- Science/engineering/math degree with computational/data science/biostatistics/bioinformatics background
- Knowledge of statistical packages.
Responsibilities:
- Interrogate micro array performance data generated by the development team to draw conclusions and make predictions based on data summaries or statistical analyses.
- Develop or implement data analysis scripts and programmes for use in various aspects of the MosaiQ development project
- Assist the development team in the design of experiments such that valid data is generated from the minimum amount of experimentation.
- Apply statistical techniques to data sets (i.e. ROC curves, CI, Bootstrapping).
- Develop programs to visualise large data sets such that process improvements can be more easily recognised.
- To work closely with Quality and Regulatory Affairs personnel to create an appropriate statistical basis for validation plans, clinical trials and other data required for regulatory submissions.
- To work closely with external collaborators as required throughout the project.
- Attend internal/external meetings and courses as appropriate and disseminate information to the development project teams.
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Clinical Pharmacy
Graduate
Proficient
1
Penicuik EH26 0BF, United Kingdom