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Develop database systems in RedCap for early detection of ovarian cancer trials of normal risk and highrisk women. The developer reports to Principal Investigator at MGH Biostatistics. The database system will accept input from sites enrolling patients in this trial including baseline information regular blood test results repeated at defined intervals cancer outcomes offstudy and end of study data. The database system will integrate the risk of ovarian cancer algorithm (ROCA) and use the demographic information from the baseline form and the ongoing blood test results to calculate a risk of having ovarian cancer and return this information to the sites with a recommendation for the next screening action.
Database developer in RedCap for early detection of cancer clinical trials. Bachelors Degree required with experience of early detection trial data biostatistics clinical research data management and development of web applications preferred.
Principal duties and responsibilities will entail
- Develop database system for high risk study
- Develop database system for normal risk study
- Develop tables to capture the data on forms used by recruitment sites to enroll patients in these studies using existing database created in Trial/DB as a template.
- Transfer existing data on all subjects enrolled in NROSS (Normal risk of ovarian cancer screening study) from Trial/DB to RedCap.
- Integrate risk of ovarian cancer algorithm (ROCA) into RedCap database as part of database system. Data from patients blood tests and patients age will form the input into ROCA and output will be a risk score which will be inserted into the database. Risk scores will be used to form recommendations for screening decisions by recruitment sites.
Skills and Competencies Required:
1. RedCap database programming
2. Web development
3. MS Office (Word Excel)
Required:
1. Bachelors Degree.
2. Understanding of RedCap database system.
Preferred:
1. Experience with early detection trial data such as NROSS.
2. Experience with development of web applications.
3. Experience with biostatistics.
4. Experience with human studies protocols
5. Experience with clinical research data management.
Required Experience:
Junior IC