Position/Title: Sr. Programmer/Sr. Data Analyst
- Description
The Sr. Programmer / Sr. Data Analyst will provide support on programming, data checking, validation of analysis results, and generation of ad-hoc analyses for clinical trials and pre-clinical research. - Responsibilities
- Work with and help direct activities of outsourcing vendors.
- Review CRFs, edit check specifications, database specifications, statistical analysis plans, and other study related documents.
- Check data, identify issues, and coordinate with CROs' Data Managers to resolve data issues.
- Validate analysis results generated by CROs.
- Produce tables, listings, figures for ad-hoc analysis to support clinical study reports, future study design, publication, and manuscripts.
- Participate in SOP development and process improvement.
- Requirements
- BS or MS in Statistics, Mathematics, Computer Science or related fields with a minimum of 5 to 7 years of SAS programming experience in the pharmaceutical or biotechnology industry.
- Skilled and experienced in Base SAS, SAS/STAT, SAS/Graph, ODS, and macro facility.
- Well organized, excellent attention to details, demonstrate and be able to deliver high quality of work.
- Proactive and be able to work independently with minimum direction and supervision.
- Works well under pressure, with initiative to take on unfamiliar tasks.
- Flexible, multiple tasking, and a team player with excellent interpersonal skills.
- Good oral and written communication skills.
- Experience with CDISC data standard and NDA submission desired.
Send resume to:
Career OpportunitiesMAP Pharmaceuticals, Inc.
2400 Bayshore Parkway, Suite 200
Mountain View, CA 94043 Or e-mail resume to: hr@mappharma.com [ back to careers ]