1. Choose your Affinity Group

* Equal Opportunity / Affirmative Action

We serve Equal Opportunity Employers and are an Equal Opportunity Employer. The Professional Diversity Network has separate professional networking sites for different affinities, and in selecting the groups you identify with, you will be joined with those networks.

Note: Providing this information is strictly voluntary - you will not be penalized or subjected to adverse treatment. If you choose not to provide this information, simply select "Choose not to identify."

2. Choose Method
X
Sign in with LinkedIn
Sign in with Facebook
OR

Tell us about yourself

Sr. Statistical Programmer II
at Vertex Pharmaceuticals
Boston, MA

Sr. Statistical Programmer II
at Vertex Pharmaceuticals
Boston, MA

Save or bookmark jobs as you go and access them anytime later with your account.

Contacts

Description

DUTIES:

Position will effectively design and code SAS programs for assigned projects;code complex SAS programs for applications designed to analyze and report complex clinical trial data and for electronic submissions of data in CDISC format with minimal instruction or input from supervisor; provide guidance on the resolution of highly complex clinical trial reporting problems within budget and timeline constraints while assuring high quality standards; perform quality control checks of advanced SAS code and output produced by other Statistical Programmers; identify problems and develop global tools that increase the efficiency and capacity of the Statistical Programming Group; conduct briefings and participate in technical meetings for internal and external representatives.

REQUIREMENTS:

The position requires a Bachelor's degree (or foreign equivalent) in Statistics, Biostatistics, Computer Science or a related field or a related field plus three (3) years of post-baccalaureate work experience in the job offered or in a related position. Experience must include the following: Three (3) years of experience working with SAS; Three (3) years of experience working with SAS with knowledge of CDISC/SDTM/ADaM; Demonstrable experience working with all SAS language, procedures and options commonly used in clinical trial reporting including the Macro language BASE SAS, SAS/STAT, and SAS/GRAPH; Demonstrable experience with electronic submissions and CDISC Demonstrable knowledge of clinical trial data, code complex SAS programs, lead and manage clinical studies.

CONTACT:

Send Resume to Shannon Holt at Shannon_Holt@vrtx.com. Reference 12140.267

Similar Jobs

See All »

Other Jobs at Vertex Pharmaceuticals

See All »