The Cambridge Group, Ltd. offers our contract employees a cafeteria-style, flexible benefits plan
where consultants can choose from:
Job 2226SO - PA - Statistical Programmer
Initial term: 6 months + extension
Rate: $40.00 - $55.00 per hour ($83,200 - $114,400 annualized)
Description:
Develop statistical analysis plans, specifications of analysis datasets, validation plans
and other related documents for an oncology study.
Requirements:
Previous NDA submission experience preferred.
BS Degree in Statistics, Computer Science, Mathematics, or a related science discipline.
3-5 years of experience in SAS programming in a pharmaceutical or CRO setting.
Contact: Stephanie Oscar - 800-525-3396 - www.cambridgegroup.com
Email:
Job 2328TP - CA - Biostatistical Programmer/Analyst
West coast firm is searching for qualified candidates to perform the following functions;
provide support to, and mentor more junior programmers, participate in process improvement initiatives
within Biostatistical Programming, generate randomization lists, assist in the review of key
study-related documents produced by other functions (e.g. CRF, Data Management Plan etc), write,
test and validate software programs to produce SDF and analysis datasets and TLGs for inclusion
within CSRs, ISS / ISE, publications and other communications, perform QC checking of software
programs written by junior programmers, manage software development, testing & release in a
Unix environment, understand and execute department-level, program-level and study-level macros and
utilities, write, test, validate program-level and study-level macros and utilities, and interface
with outsourcing partners and vendors at project level.
Qualified applicants must possess a BS/BSc or higher degree in Computer Science, Statistics,
Mathematics, Life Sciences or other relevant scientific subject, and have a minimum of 3 years
of relevant experience in a clinical trial programming role in a pharmaceutical environment.
You should also have a firm understanding of the drug development process and understand the role
of biostatistical programming within that process.
Contact: Traci Palmer - 800-525-3396 - www.cambridgegroup.com
Email:
Job 2276TP - CA - Sr. SAS Statistical Programmer
West Coast firm is seeking a seasoned SAS professional to work collaboratively with Biostatisticians,
Statistical Programmers, Clinical Research Associates, Clinical Data Managers and other Clinical,
Global Drug Safety, Regulatory and Project Management staff to meet project deliverables and timelines
for statistical data analysis and reporting.
Primary responsibilities of this position include; identifying potential issues in statistical analysis
plans and proposes solutions, assessing the quality of analysis data, performing cross-study analyses,
using internal macros or writes SAS® macros to automate statistical table, figure, and listing production
mentors junior programmers, assisting in the preparation of submissions of electronic data
(e.g., SAS® data sets) to regulatory agencies, independently develop analysis file programs, and work
as a primary programmer for one or two Phase 1-3 studies and as a secondary programming contact for one
Phase 1-3 study.
The qualified candidate will possess a BS degree in Biostatistics/Computer Science or equivalent with a
minimum 6 years of relevant industry experience, or a MS degree in Biostatistics/Computer Science or
equivalent and minimum 4 years of relevant industry experience in the statistical analysis of biomedical
data using SAS® software. You must also have excellent verbal, written, and interpersonal communication
skills and have a thorough knowledge of clinical trial study design and electronic data submission requirements.
In addition, you must be able to work independently on multiple concurrent projects, be capable of
attending study team meetings as the primary statistical programming contact, and have the ability to
communicate with external vendors (e.g., Contract Research Organizations) regarding electronic submission issues.
Contact: Traci Palmer - 800-525-3396 - www.cambridgegroup.com
Email:
Job 2310BG - NJ - Statistical Programmer II
Southern NJ firm is searching for candidates with at least 2 years of SAS programming experience in
a clinical trials environment to serve as the core project team member to design and specify the
overall approach to a project's programming tasks. As you support statisticians with computer
programming tasks, you will generate summary tables and data listings, produce graphs, and process
lab data, as specified in statistical analysis plan. You will also generate derived SAS datasets for
all parameters and ensure consistency among tables/listings and create, test and maintain SAS programs
for clinical studies according to departmental standard procedures. In addition to your SAS experience,
you should possess a Bachelor's Degree, preferably in computer science, statistics or a related area,
and have effective verbal and written communication skills.
Contact: Bonnie Grettler - 800-525-3396 - www.cambridgegroup.com
Email:
Job 2279TP - MA - Senior Statistical Programmer/Analyst - Biosurgery
Working at this Northeastern biotechnology company, you will support clinical development by
statistical programming of clinical study tables, listings, and figures. The ideal candidate will
have clinical trial experience (phases I-IV) with 3-5 years of experience. Candidates with SAS
programming experience in a regulated industry will be considered. A Bachelor's degree is required,
with a graduate level degree preferred.
Contact: Traci Palmer - 800-525-3396 - www.cambridgegroup.com
Email:
Job 2240BG - NJ - SAS Programmer II
Join this CRO as a senior statistical programmer. In this role, you will report to the manager,
statistical programming and be responsible for leading the development and maintenance of analysis
programs to support clients' drug development projects, leading the communication of technical issues
with lead client staff and internal team staff, and contributing to internal technological advances.
The Primary Responsibilities will be; leading the implementation of data listing, summary, and graphs
for inclusion in new drug applications (NDAs), contributing to the development of and training on
Standard Operating Procedures (SOPs), developing software for standard operating systems, providing
technical consult on clients’ needs to Operations staff, and troubleshooting as required for staff
and clients regarding specific programming concerns. You will also; review listing, summary, graph,
and tabulation specifications, provide secondary review of statistical programming deliverables,
develop standard programming procedures, and support programming needs within Operations.
Qualifications include a BA or BS in computer science, statistics, mathematics, or information
technology. Also required are at least two years programming experience with demonstrated
leadership skills at a CRO or a Pharmaceutical company with clinical trial experience.
Extensive knowledge of SAS and knowledge of C, C++, Pascal, or other high-level 3rd or 4th
generation languages is preferable. Exposure to pharmaceutical, biotechnology or device industry
highly desired. Equivalent combination of education and work experience may be substituted.
Contact: Bonnie Grettler - 800-525-3396 - www.cambridgegroup.com
Email:
Job 2311BG - NJ - Senior Statistical Programmer
Do you have at least 5 years of SAS programming experience in a clinical trials environment?
Are you presently located in Southern NJ?
If so, then utilize your skills to serve as the core project team member to design and specify
the overall approach to a project's programming tasks. As you support statisticians with computer
programming tasks, you will generate summary tables and data listings, produce graphs, and process
lab data, as specified in statistical analysis plan. You will also generate derived SAS datasets
for all parameters and ensure consistency among tables/listings and create, test and maintain SAS
programs for clinical studies according to departmental standard procedures. In addition to your
SAS experience, you should possess a Bachelor's Degree, preferably in computer science, statistics
or a related area, and have effective verbal and written communication skills.
Contact: Bonnie Grettler - 800-525-3396 - www.cambridgegroup.com
Email:
Job 2280TP - MA - Statistical Programmer/Analyst
Northeastern biotechnology firm is seeking an experienced SAS Programmer to support clinical
development by statistical programming of clinical study tables, listings, and figures. The
ideal candidate will have clinical trial experience (phases I-IV) with at least 5 years of
SAS experience. Candidates with SAS programming experience in a regulated industry will be
considered. A Bachelor's degree is required, with a graduate level degree is a plus. Biotechnology
or pharmaceutical industry experience preferred. The ideal candidate will be able to work
independently and in a team setting, have excellent communication skills, and produce quality
deliverables. A working knowledge of Base SAS, SAS Macro, SAS Graph, SAS Stat is required.
Contact: Traci Palmer - 800-525-3396 - www.cambridgegroup.com
Email:
Michele Leone Stumpf
