The CLEAR Working Group is looking for a clinical information analyst to help reduce the burden of hospital readmissions by developing strategies and conducting research for a pilot clinical trial for bladder cancer patients.
Requirements
- 3 years of experience in analyzing and interpreting processes and clinical outcomes.
- Experience in working with a database and project/program management and with management of clinical trials.
- Efficient in RedCap, Microsoft Word, Excel and Powerpoint.
Responsibilities
- Gathers, analyzes, and interprets data and clinical trial data to identify opportunities to improve the quality of care for patients
- Prepares reports based on measures of processes and outcomes of care
- Serves as a clinical trial project manager for a pilot trial including
- Regulatory oversight including IRB process and compliance with ClinicalTrials.gov
- Screening, consent and enrolment of patients into trial
- Data entry and management
- Training, and support of study team members both internally and externally
Other
- Bachelor's degree
- Excellent interpersonal and communication skills (both written and oral).
- Ability to work in a team, as well as be self-sufficient, motivated and organized.
- This is a 2 year term-limited appointment.
- Positions that are eligible for hybrid or mobile/remote work mode are at the discretion of the hiring department.
