Public Health Job Opportunities

Statistical Data Analyst/Programmer

We are currently looking for a candidate to fill the position of Statistical Data Analyst/Programmer here at the Center for Administrative Data Research at the Washington University School of Medicine, Saint Louis, Missouri.

 

POSITION SUMMARY:

The individual in this position provides data management and programming expertise for the Institute for Clinical and Translational Sciences (ICTS) Center for Administrative Data Research (CADR). The studies will primarily use individual and longitudinal administrative health care billing and claims data. Continue reading “Statistical Data Analyst/Programmer”

Senior Outcomes Research Associate

Optum, in Rhode Island, is seeking a Senior Outcomes analyst. This would a be an opportunity most appropriate for a PhD graduate with strong quantitative skills and a fluency in SAS.

A former COPH faculty member, Dr. Asia Sikora Kessler currently works at Optum and is happy to answer questions to anyone interested (contact Career Services for contact info).

View the job description and apply online here.

Health Data Coordinator

The Fred and Pamela Buffett Cancer Center, Clinical Trials Office is seeking a Health Data Coordinator to be responsible for the collection and review of clinical protocol research data; Interpretation of data (including appropriate source documentation) for entry into computerized databases; Creation of data definitions and case report forms and other information related to data collection for clinical research. Provide support to the clinical study coordinators through data collection, scheduling, research protocol management, and other administrative duties.

 

View the full job description and apply online here.

Data Quality Monitor

The Fred and Pamela Buffett Cancer Center, Clinical Trials Office is seeking a Data Quality Monitor to implement a quality assurance strategy to ensure compliance with all applicable regulatory requirements. Develop and implement detailed audit plans and SOP’s, managing the internal auditing functions consistent with GCP/GMP requirements. Responsible for the process that verifies data collected is accurate and reliable. Serves as a content expert. Ensure all processes contributing to the performance of the clinical trials are conducted in accordance with ICH/GCPguidelines to ensure high quality and integrity of the research data.

View the job description and apply online here.