Evaluation and analysis of disease progression in neurodegeneration.
Experience in efficiently handling MRI and Statistical analysis of the WiRMS Clinical Trial at Nottingham University Hospitals NHS Trust, Queens Medical Centre.
Efficiently supporting the clinical trial and liaising closely with lead study investigator, statisticians, data managers and multidisciplinary project teams.
Proficient in managing large amounts of complex, real-world, digital health records and, provided data management, manipulation and analysis expertise and support to the team of statisticians and clinicians.
Efficiently managed the clinical data on the Nottingham Clinical Trials Unit database, which comprises of numerous randomised patients for the immunomodulation therapy.
Efficiently supporting the clinical trial by providing meticulous data management.
Design and maintain databases, queries, reports, graphics and data-analysis tools; effectively perform data entry, check reviews, database audits and coding; and define and validate study protocols.
Interpret, synthesize and present technical information to supervisors, management, funders and pharmaceutical and biotechnology teams.
Oversee data-management lifecycle of the clinical trial, composing and verifying reports and results.
Develop clear clinical data sets enabling the standardized collection and analysis of massive amounts of cross-boundary data content in a timely manner and with a high level of accuracy.
Efficiently performed evaluation of treatment and interpretation of research findings to adjudicate disease outcome status among numerous participants recruited in the clinical trial.
Excellent experience of playing a significant role in database management in a randomised clinical trial.
Expertise in statistical modelling and analytical techniques to address specific research aims.
Efficiently worked in all phases of data cycle such as case evaluation, data extraction and validation and data visualization.
Responsible for the preparation of written reports and manuscript for peer-reviewed, high-quality publication.
Effectively track progress of clinical studies, ensuring projects meet timelines and quality expectations.
My expectations for the company would be to provide a work environment in which I can contribute to the team, I receive appreciation for my contributions, I have job stability and the ability to grow with the company.
Expected Base Salary
**,000 GBP / year
Expected Hourly Rate
Total Professional Experience
Send a connection request to the candidate to get their contact details.Contact Candidate