• If you are looking to join a fast growing dynamic CRO.
• If you enjoy working in a team-oriented entrepreneurial environment .
• If you like the feeling that your contributions make a difference and do not like the feeling of being a small peon in a large organization .

This person's key responsibilities are:
• Design randomization schedules for random treatment assignment
• Develop statistical design and analysis methods for Phase I through IV clinical trials
• Perform power and sample size calculations
• Write statistical section of protocol
• Design and perform interim analyses
• Communicate with clients and advise them on statistical issues of study design and interpretation of statistical analyses
• Supervise and guide other statisticians in the team
• Interact and consult with clients.
• Design statistical models using SAS in accordance with study protocol and/or Statistical Analysis Plan.
• Programming and performance of statistical analyses as described in a clinical study Statistical Analysis Plan and/or a study protocol .
• Writing statistical report

• Proficiency with a computer using Windows, Windows 95/98/2000 or NT.
• Proficiency in SAS statistical PROCs to perform statistical analyses.
• Familiar with MS Office suite.
• Strong written and oral communication skills.
• Knowledge of clinical trial methodology and processes

The initial project that this position will be working on is developing applications on a new and exciting web deployed data warehouse. This is a really exciting and career building opportunity for the right candidate. The duties include supporting some legacy applications. The position will be primarily writing code and performing unit testing. We typically have a simple written unit test plan that the developer writes, gets approval on, and executes.

Desired skills include:

Note: Client company is not offering visa/transfer sponsorship at this time.

System development is primarily web-based and will focus on major initiatives such as moving core business functions to the web, a SAS Data Warehouse, Customer Relations Management and Knowledge Management systems. We have web systems that integrate SQL Server procedures, HTML, ASP, and Java with SAS macros and a SAS AF application. Experience with other programming languages and non-SAS environments is helpful. Compensation commensurate with experience.

• Interacts with statisticians/DBAs/Reviewers to determine the data processing requirements and database structure for clinical studies (10%).
• Designs/codes/tests/debugs/documents/implements software needed for summarization, reporting, analysis and checking of clinical trial data independently (40%).
• Utilizes/modifies standard programs & systems to generate displays/listings/graphs for the presentation of clinical trial study results (40%).
• At least three years of clinical trial data processing esp. Extensive programming skills with SAS software for data manipulation, statistical analysis, reporting summarization & graphing.
• Result oriented, customer focused, thinks strategically, team interfacing skills, good communication skills.
• The candidate must have worked the last two to three years with SAS in a clinical trials area.

(Cardiovascular/Metabolic/Endocrine/Gastrointestinal) studies. Employ standardized programs where applicable. Provide input into planning documents such as protocol, validation plan, and report and a

• BA/BS or equivalent experience in computer science, mathematics, statistics, life sciences, or related field(s).
• Intermediate SAS programming skills, with 2-5 years experience in a medical setting, preferably working with clinical trials data.
• Good understanding of clinical trial practices, procedures and methodologies.
• Good verbal and written communication skills.
• Good interpersonal and organizational skills.
• Attention to detail and correctness.
• Working knowledge of office tools.
• MS in Statistics is a plus.

JOB SUMMARY:

MINIMUM REQUIREMENTS:

Technical Skills:

To be considered for these positions you must have a minimum of a Bachelors degree and 3+ years experience working on Pharmaceutical Clinical Trials Phase I-IV as a SAS PROGRAMMER.

The Load Profiling Analyst performs daily operation of profiling functions such as research, sampling, statistics and electric load profiling. Involved in the profiling computing systems development, testing of new software applications, and development of business processes and procedures. Will assist in load research sampling, data collection, and analysis required to support load profiling. The Load Profiling Analyst helps ensure that load profiles are properly designed, applied and maintained.

To be considered for this position you must have 3+years of SAS, and 2+ years of MetrixND. You will also have minimum of 4 years working with metering systems for the electricity power/energy market.

Experience and Educational Requirements

To be considered for these positions you must have a minimum of a Bachelors degree and 3+ years experience working on Pharmaceutical Clinical Trials Phase I-IV as a SAS PROGRAMMER.

Experience:
Proven experience in SAS programming in clinical trials for a minimum of 2 years. Knowledge of a variety of different SAS modules including BASE, STAT, GRAPH, MACRO. Able to work within a team environment with genuine enthusiasm and commitment. Clear and effective communication skills. Ability to write concise and accurate documentation. Understanding of Windows, knowledge of Excel, Word, familiarity with the Clintrial system. Awareness of clinical trial and clinical data management processes. Relevant industry experience in programming for clinical trials including regulatory submissions.

Job Details:
Programming support and advice to statistics and data management. Develop, test, validate, implement, document and maintain the department¹s software library. Produce tables, listing and graphs for clinical study reports. Interact with Regulatory Affairs in support of electronic submissions. Importing and exporting data files. Manipulating and validation of data transfer and transformation programs. Develop and maintain appropriate SOP¹s. Identify and implement data management tools in line with the industry. Train users in new applications.

Description of Duties and Responsibilites:

Requirements:
2-3 years SAS programming, including statistical procedures and macros. Statistics degree and Pharmaceutical experience a plus. Good communication skills.

Our client prefers for somebody with experience in setting up studies in Oracle Clinical (data definition, validation procedures, and derivation procedures). A total of 1 or more year’s experience in PL/SQL and or/SAS programming and experience in the Pharmaceutical industry are required. You must have knowledge of relational databases. Previous experience with electronic data transfer and upload into Oracle Clinical poses a distinct advantage.

Same client seeks a proficient Statistical programmer / consultant to come on site for an indefinite period of time. You will be responsible for the programming involving various pharmaceutical products in the phase III or post marketing development. The project is to create an analysis data set then set up and run the statistical test as prescribed by the senior statistician; then produce reports.

Technical Skills:

Trilogy Consulting seeks 3 Clinical SAS Programmers / consultants. You will be responsible for performing analysis on clinical trial data, including listings, tabulations, graphical summaries and formal statistical estimates and tests. Must be able to assess quality of analysis data, perform cross study analysis and use SAS Macros to automate all of the above functions. You will develop analysis datasets and assist in the preparation of NDA's. A bachelor's or Masters degree in Statistics or Computer Sciences supported by 3- 4 years of industry experience. Good oral and written communication abilities and analytical skills are essential.

Technical Skills:

Technical Skills:

We have more openings with the same client for a Capacity Planner / SAS Programmer. Must have a minimum 5 years with industry experience performing capacity planning. Strong familiarity with MICS, MXG or similar tools is desired; as well as experience in a Unix environment, with SUN systems. Experience with performance monitoring of Windows NT systems. Will require gathering performance information on CPU utilization, workload analysis, memory and storage availability, and other system performance measurements.

Desired Skills:

• 40% Programming and document timely and quality clinical listings and summaries for inclusion in worldwide health registration and NDA submissions. Respond to ad-hoc business requests for tables and listings.
• 35% Lead the design and development of analysis and reporting databases.
• 15% Provide oversight and mentoring of Clinical Programmers.
• 10% Assist programming manager/supervisor in project planning, manpower projections and resource allocations across therapy areas. Interface with programming manager/supervisor to assure consistency of technical and process strategies across all therapy areas.

Background Requirements

• Relocation Assistance
• Direct Deposit
• Two Weeks Paid Vacation Each Year
• Nine Paid Holidays
• Paid Sick Leave
• Matching 401K
• Medical / Dental / Life / Vision / Long Term Disability Insurance
• Flexible Spending Plan
• Employee Benefits Program
• Employee Stock Purchase Program
• Paid Overtime
• Comp Time (save your overtime hours)

JAS Associates represents over 25 companies, including CRO’s, Pharmaceuticals and Biotechs, on primarily the East Coast, as well as in Texas, Illinois, and California.

Within the areas of concentration listed above, JAS Associates has positions at all levels in the company’s hierarchies, from entry level through Executive Director.

SAS Programmer:

Principle Programmer:

Manager of Programmers:

• Paid Work Visas
• Paid Holidays
• Sponsorship for Green Cards after 30 days
• Relocation Assistance
• Paid Vacation/Sick Days
• Medical and Dental Insurance
• 401k (after 3 months)
• Education Assistance

• Market research and analytic skills
• Knowledge of life and/or health insurance products
• Strong mathematical and analytical skills
• Effective writing and communica-tion skills
• Experience with PC analytic software (Microsoft Access, Excel), SAS or database analysis software
• The ability to work in a team setting and work on multiple projects
• MBA, Masters or equivalent experience

Role: Consultant, SAS guru, exceptionally nice person
Salary: $60,000 - $85,000 (Negotiable based upon your experience.)
Position Type: Full Time (Cary, North Carolina)
Ref Code: SPT32801

We are looking for senior software developer to join our organization. We are a high-tech, software development/ consulting organization and are looking for people who are high in accountability, motivation and responsibility. Consultants will work on a variety of client-based projects in the various industries developing decision support, information systems (primarily web-based).

This candidate should have a thirst for learning as well as mentoring both internal and external constituents. Great communication skills (both oral and written) are essential. This is an ideal position if you like to see the whole picture, don't like corporate politics and believe in the enduring values of integrity, quality and teamwork.

This person will have at least 5-7 years in a professional software development environment. This flexible, knowledge-oriented person will have had hands-on development experience in building both client/ server and web-based applications. A strong understanding of object-orientation is desired. We work with a variety of clients using cutting-edge technologies like SAS/IntrNet, SAS Warehouse Administrator, AppDev Studio, enterprise clients (AF, webAF, web, macros). This person will have an exceptional ability to help translate business problems into technology solutions. By blending their skills as a designer, developer, database guru and personality, they will make a significant contribution to a fast-growing company.

Required Skills:
Base SAS, SAS IntrNet, Warehouse Administrator, Macros, Connect, Share HTML, JavaScript and other client-side development languages Unix, Windows NT (other platforms such as VMS, MVS, CMS would be desired)

Desired Skills:
JSP, Java, ASP, Servlets and other server-side, web technologies Familiarity with XML, XSL, and/or model mapping techniques Software development life-cycle tools (e.g., Requirements management, Analysis design; visual modeling (UML); Configuration and change management; Software testing) Microsoft Office Development (Word, Excel, PowerPoint, Access, Project) Oracle, LDAP, Rational Enterprise Suite, Transaction Server, Visual Basic (5 and/or 6), Microsoft Web Server technologies (IIS, ASP, InterDev, VBScript); SQL Server 7.0 with Transact SQL or Oracle with PL/SQL Data Modeling, Data Mining or enterprise data and application integration; experience in dealing with COM/DCOM/ Corba.

Other skills:
Demonstrated project-management skills. Ability to conceptualize client needs and translate into specific implementation strategies. Excellent knowledge of programming principles and user interface issues. Superior programming, analytical, and problem-solving skills. Ability to work independently or with a team.

Additional Information:
Must be eligible to work in the U.S.
Must be able to travel up to 30-50%