Clinical Statistical Progammer

Excellent opportunity for a contract Statistical Programmer with a growing Biotech Company in Los Angeles, Calfornia!

RESPONSIBILITIES:

- Program TLGs using SAS for the purpose of clinical study report.  This may include ad-hoc analyses.

- Understands CDISC and perform its associated mapping programming requirements.

- Understand 21CFR Part 11.

- May serves as verifier of other programmer's deliverables.

- A team player who is willing to perform assigned projects.

- Exhibits flexibility by assuming other unplanned requests/assignments. 

QUALIFICATIONS:

- Minimum MS (Biostatistics/Statistics) with 2+ years of Clinical Programming experience.

- Good communication skills.

- Ability to work well independently and with a team.