Description
One of San Francisco Bay area's leading pharmaceutical providers is now recruiting for a clinical data programmer.The Clinical Data Programmer is responsible for both EDC and Report (listings) Programming on assigned studies. This is conducted by performing system setup and testing following standard process procedure and SOP.
Primary Duties
- Leads and coordinates the design and testing of clinical study databases to match CRFs according to company standards.
- Assist in database upgrades/migrations including testing
- Maintain appropriate documentation surrounding maintaining or archiving clinical data and/or programs.
- Responsible for managing data transfers between with CRO's and Vendors.
- Ensures timely completion of tasks assigned with quality
- Some travel may be required
- Other Duties as assigned.
- Advise data management on reporting tools for custom reports
- Ensures clinical study databases are integration ready
Required Qualifications and Experience
- Bachelor in Computer Sciences, Mathematics, Life Sciences with a minimum of 2 - 5 years of clinical programming experience in the pharmaceutical or biotechnology industry, or MA/MS with 2 years of experience
- Clinical programmer experience in a pharmaceutical or CRO working in a FDA regulated environment
- Some knowledge of ICH, FDA, and GCP regulations and guidelines; Knowledge of CDASH, SDTM and CDISC
- SQL or SAS programming skills preferred
- EDC Systems; Medidata Rave and Lab Admin experienced preferred
- Reporting tools; JReview, BOXI
Compensation
This pharmaceutical provider is very eager to hire and encourages all interested applicants to apply as soon as possible. This is a 1 year contract, with potential for extension or conversion. Do not hesitate to apply today.