CyberDivan Recruiting SAS Jobs
From sasCommunity
The CyberDivanspecializes in the Recruitment and Placement of Personnel Working in Clinical Trials for Pharmaceutical Companies, Biotech Companies and Contract Research Organizations.
Current SAS Openings:
[edit] SAS Senior Statistical Programmer/Analyst
JOB STATEMENT: The primary focus of this position is to perform and lead statistical programming tasks associated with Phase 1, 2, 3 and 4 clinical trials for new drug and biological products, as well as medical devices. ESSENTIAL JOB FUNCTIONS: • Develop policies and procedures. • Provide leadership and work on multiple clinical projects • Train/mentor statistical programmers. • Successful completion of programming tasks on time and on budget • Expected to provide leadership in new technologies and procedures for improved efficiencies. • Design, develop and test SAS software to implement Program Analysis Specifications (PAS) for multiple projects. • Document and validate SAS software development according to Biostatistics standard operating procedures. JOB REQUIREMENTS / EDUCATION / EXPERIENCE: • Bachelor or Master’s degree in a scientific discipline, preferably Statistics or Computer/Health Science. • Minimum of three to five years Statistical Programmer Analyst III experience relevant biopharmaceutical industry experience. • Ability to train/mentor statistical programming support staff. • Knowledgeable about regulatory and ICH Guidelines as it pertains to project support. • Excellence in interpersonal, verbal and written communication skills a pre-requisite for advancement.
Location: Atlanta, GA
[edit] SAS Principal Analyst II
Job Description: Contribute to computer programming efforts for a clinical trial drug project and to provide programming support for clinical trial data reporting and regulatory submissions. Assumes protocol level and some project management responsibilitywhile supporting the Programming and Statistics lead. Able to support multiple protocols independently and to contribute to integrated summaries of efficacy and safety. Demonstrates strong SAS programming skills participates in protocol team and some project team interactions. Builds successful relationships and seamless interfaces at the protocol project team level. Provides timely and effective communication to the programming and statistics leads. Education Requirements: MS/MA is required Experience Requirements: Experience in SAS programming related to clinical drug development. Familiarity with data management principles and exposure to requirements for statistical computation regarding layout and presentation of data to support programming analyses. Significant academic training in computing, statistics, or other scientific discipline MS/MA or equivalent experience required at least 4 years relevant experience in the pharmaceutical industry
Locations: Hopewell, NJ & Wallingford, CT
[edit] SAS Technical Manager
Job Description: Responsible for the development and implementation efforts for the globalization, improvement, and standardization of processes and systems that support clinical trial data reporting and regulatory submissions. Contributes to theproject leadership of an indication for a late stage development program. Demonstrates advanced SAS programming skills evaluates processes in order to increase efficiencies and develop innovative strategies and technologies for flexible and global clinical trial reporting. Negotiates within the department and cross functionally, building successful partnerships and seamless interfaces. Provides timely and effective communication to team members, highlighting GBS goals and priorities, ensuring work efforts parallel departmental objectives. Supports teams by providing technical direction, coaching and feedback to programmers. Provides input into the development and technical training needs of programmers. Familiarity withdata management principles and exposure to requirements for statistical computation regarding layout and presentation of data to support programming analyses. Education Requirements: MS/MA is required Experience Requirements: Significant academic training in computing, statistics, or other scientific discipline MS/MA is required and at least 6 years SAS programming experience in the pharmaceutical industry and some experience supervising technical resources.
Locations: Hopewell, NJ & Wallingford, CT
