• Weekly Payroll
• Direct Deposit
• Personalized business cards
• Medical/Dental Options (Keystone and Guardian. For Central PA area Capital Blue Cross is also offered)
• Group Short Term Disability, Long Term Disability, Life and AD&D coverage
• Payroll Deductions for Benefit Elections.
• 401 (K) plan
• Consultant Newsletter

Seeking an self-motivated, experienced Statistical Programmer with strong SAS and Visual Basic experience to develop key sales management consulting initiatives by providing state of the art programming support. Develop SAS programs to explore and analyze physician level prescription data, and utilize Visual Basic to develop applications. This position will continually require innovative thinking on conceptual products and services, state of the art statistical programming, and independent personal development in new technology.

The candidate should have a Master's degree in a quantitative science and at least five years of relevant experience, or Bachelor's plus 8 years of experience. Should be capable of developing complex but efficient SAS code combining data across time. Also requires the ability to meet critical deadlines and handle multiple priorities, clear oral communications concerning the technical aspects of a project, and the ability to develop usable documentation. Experience with SQL Server is a plus.

LOCATION: Blue Bell, PA
CONTACT: Jodi
POSITION Title: Statistical Programmer w/ SAS and VB
LENGTH of Contract: Permanent
Email:
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http://www.devonconsulting.com/SubmitResume.htm

Our Fortune 500 client is seeking a SAS Programmer with 4 years experience in clinical trials. The ideal candidate will have an indepth knowledge of SAS and statistics. Must be familiar with Regulatory Agencies requirements and experience with integration of data and validation techniques. Knowledge of Unix is a plus.

LOCATION: Clifton, NJ
CONTACT: Melanie
POSITION Title: SAS Clinical Programmer
LENGTH of Contract: Permanent
Email:
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IT Group requires additional SAS Developer with a minimum of 2 years of experience to join respiratory group for development and report analysis for FDA clinical trail evaluation. The position requires a clinical background, and the ability to work independently, meet deadlines, and meet manager's report requests. The work environment is business casual and offers independent work space.

LOCATION: Wilmington, DE
CONTACT: Jodi
POSITION Title: SAS Developer w/ Clinical background
LENGTH of Contract: 6 Months
Email:
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Provide programming support and validation of analysis datasets, pooled datasets, listings, summaries, figures and tables for Phase IIV clinical trials, ISS and ISE. Provide programming support and validation of data structures and database applications, input into specifications, and input into documents for assigned projects. Provide necessary programming support for internal and external transfer of electronic data. Maintain consulting, training, and support with internal and external customers. Assist in the formulation of SOP?s and guidelines, and actively review and monitor compliance.

Provide input into electronic submissions, and necessary output for the compilation of statistical appendices for CTR, ISS and ISE. This position requires a Bachelor's degree or equivalent experience in computer science, mathematics, statistics, life sciences, or related fields. Also requires intermediate programming skills with knowledge of database design and SAS software, and a good understanding of clinical trial practices and procedure methodologies. Should have excellent verbal and written communication skills, as well as good presentation, interpersonal, and diplomacy skills. The ideal candidate has a continuous improvement orientation with excellent organizational skills and a working knowledge office tools.

LOCATION: East Hanover, NJ
CONTACT: Pat
POSITION Title: Clinical Programmer/Analyst w/ SAS
LENGTH of Contract: 6 Months
Email:
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Seeking a SAS Programmer / Clinical Analyst with 5+ years of work experience to provide programming support and validation of data structures and database applications for Phase IIV clinical trials, including data consistency checks and monitoring reports. Provide input into specifications of analysis, datasets, pooled datasets, listings, summaries, figures, tables, data structures and database applications for Phase IIV clinical trials, ISS, and ISE. Provide input into documents for assigned projects. Provide necessary programming support for internal and external transfer of electronic data. This position requires a Bachelor's degree or equivalent experience in computer science, mathematics, statistics, life sciences or related field.

Should have a working knowledge of database design and creation of clinical database applications using Clintrial 4, as well as the ability to program basic monitoring reports in SAS. Als requires strong knowledge of global clinical trial practices, procedures and methodologies, excellent verbal and written communication skills, and excellent presentation, interpersonal, and diplomacy skills. The ideal candidate will have a continuous improvement orientation with strong organizational skills and knowledge of office tools.

LOCATION: East Hanover, NJ
CONTACT: Pat
POSITION Title:Clinical Programmer/Analyst w/SAS and Clintrial 4
LENGTH of Contract: 3 Months
Email:
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Seeking a SAS Programmer with 3+ years of experience to program, test, and validate clinical trial listing, counts, query, and integrated summary reports in the SAS and SAS Macro Languages. Will interface with internal client community to define detailed programming requirements and support the client community in adhoc queries and investigations of clinical trial database. Will be part of a strong team environment dedicated to the support of clinical and vaccine products as well as the development of sophisticated tools which assist the staff in providing service to our internal client community. A 24 week training period will be provided involving the details of the clinical trial database and associated query language, departmental SOP's, and tools and utilities available to the staff for successful support of vaccine and drug products. This position requires sound programming methodologies and testing/validation procedures. Detailed documentation required. Should have project leader experience or capability. Knowledge of relational database technology is a plus.

LOCATION: Blue Bell, PA
CONTACT: Jodi
POSITION Title: SAS Clinical Trial Programmer
LENGTH of Contract: 5 Months
Email:
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• a.. 6+months Pharmaceutical Industry experience
• b.. Use SAS to analyze clinical trial data and to produce tables, listings, and graphs
• c.. Program SAS edit checks for data cleaning
• d.. Documentation of programs adhering to regulatory and corporate standards
• e.. QC of programs
• f.. Expertise in SAS/BASE
• g.. Familiar with SAS/MACRO, SAS/STAT

Primary duties will include analysis, design, coding, implementation, testing and documentation.

Secondary responsibilities will include Unix SAS administration duties and providing assistance to customers using SAS. Work will include new product development, ad hoc analysis support and possible maintenance and enhancement of existing processes.

The job is classified as a full-time, junior level position (guaranteed for 3 years, possibly more). We need someone with several years of SAS programming experience (BASE primarily, also FSP/AF would be helpful). A background in Computer Science or Statistics would be helpful (or experience working with research studies). Salary is commensurate with experience.

We need to fill this position as soon as possible.

• a.. 6+months Pharmaceutical Industry experience
• b.. Use SAS to analyze clinical trial data and to produce tables, listings, and graphs
• c.. Program SAS edit checks for data cleaning
• d.. Documentation of programs adhering to regulatory and corporate standards
• e.. QC of programs
• f.. Expertise in SAS/BASE
• g.. Familiar with SAS/MACRO, SAS/STAT

Tasks:

Start Date : ASAP
Duration : 18 months
Location : Upper Mid West

Summary of Duties: Enhance and support existing applications as well as design and develop new application for clinical studies. Develop and maintain documentation for projects. Assist with or provide programming support for special clinical projects.

Experience, Education, and Qualifications/Certification Guidelines:

SENIOR STATISTICAL PROGRAMMER

Statistical Programmer (Wilmington & RTP)

Biostatisticians (Wilmington & RTP)

The PharmaResearch reputation for quality, stability and scientific achievement is supported by a progressive compensation/benefits package.

• Weekly Payroll Direct Deposit
• Personalized business cards
• Medical/Dental Options (Keystone Health and Guardian Dental. For Central PA area, Capital Blue Cross is also offered.)
• Group Short Term Disability, Long Term Disability, Life and AD&D coverage
• Payroll Deductions for Benefit Elections.
• 401 (K) plan
• Consultant Newsletter

Clinical Applications Programmer

STATISTICAL PROGRAMMER Research and Development

STATISTICIAN Research and Development

ASSISTANT MANAGER SEGMENTATION ANALYST

Risk Management

Senior Scoring Analyst

Smith Hanley, one of the largest and most respected statistical recruiting firms in the country, has many immediate openings throughout the United States for long-term, stable consulting positions with solid Pharmaceutical and Bio-Tech companies.

For our consultants, we offer competitive and flexible salary plans (with benefits or W-2) or sub-contract with corporations. We also offer competitive fees for referring a candidate who is hired by us. Please contact the person listed below for further details.

Smith Hanley Consultant Benefits

Philadelphia (3 positions, 6-12 month assignment+renewal) 1-3 years experience in research, hospital or pharmaceutical industries, SAS Base, Stat, Macro programming, and experience with the manipulation of large clinical data sets. Mainframe and VMS OS experience a plus. Experience with AF & SQL also desired.