Available candidates                          programmers & biostatisticians

 

DataCeutics will from time to time announce programmers and biostatisticians available for placement into pharmaceutical and biotech organizations.  Our resources are highly-experienced, self starters whose careers are devoted to the pharmaceutical & biotech industry.

 

CV - profile 101

Senior Consultant, Clinical SAS Programmer Analyst - 15 years +

A skilled Clinical SAS Programmer Analyst with over 15 years of experience in the pharmaceutical industry. He is adept at producing tables, listings, figures and datasets to support the analysis of all phases of clinical trials and he has worked closely with statisticians to provide accurate and timely statistical analyses. Capable of providing statistical expertise on all analyses involving logistic regression and he can easily develop standard macros and tools for data analysis and reporting. He has established and implemented programming standards to comply with regulatory requirements such as CDISC (ADaM and SDTM datasets) across all studies and has led and provided input into technical initiatives in order to develop and strengthen standard processes within analysis and reporting. He has trained and mentored programming personnel and is a strong communicator that would be an asset to any team.

 

cv - profile 102

Senior Consultant, Clinical SAS Programmer Analyst - 25 years +

Over 25 years of clinical experience within the pharmaceutical industry. Since 1989, he has been a SAS Clinical Programmer and Biostatistician for pharmaceutical and biotech companies.  He has created safety and efficacy tables, listings and graphs related to clinical trials and has been involved in building CDISC datasets. He has supported FDA submissions and approvals and supported validation of SAS programs for clinical trials in a UNIX environment and has helped to write SAS programs to independently duplicate Safety and Efficacy tables, listings, Kaplan-Meier survival graphs and analysis datasets. He has created CDISC ADaM and SDTM datasets in Epidemiological for incidence rates of patients from database registries. 

 

cv - profile 103

Senior Consultant, Clinical SAS Programmer Analyst - 30 years +

Over 30 years of experience in BASE SAS, SAS MACROS, SAS/ACCESS, & SAS SQL.  Experience working in Phases I - III of Clinical Trials related to various therapeutic areas such as Cardiovascular, Rheumatoid Arthritis, & Oncology. Experience working on multidisciplinary teams & also capable of completing independent research projects. Creates SDTM & ADaM datasets for submissions to regulatory authorities like the FDA.

 

CV - PROFILE 104

Senior Consultant, Clinical SAS Programmer Analyst - 12 Years

Twelve years of SAS programming experience supporting Phase I-III clinical trials. Extensive lead experience & has served as a Programming Manager. Experience with CDISC Standards (SDTM & ADaM). Works on teams & creates tables, listings & graphs following CDISC standards. Has great communication & interpersonal skills.

 

CV - PROFILE 105

Senior Consultant, Clinical SAS Programmer Analyst - 13 Years +

A Senior Consultant, Clinical SAS Programmer Analyst with over 13 years’ experience. He has worked in a SAS Programming group and was responsible for managing and developing the Phase I Statistical and Database Programming group and is also responsible for the programming for Phase I. He has also supported Phase II-III clinical trials, and has worked on several successful ISS/ISE submissions.  He has extensive experience with tables, listings and graphs as well as working with CDISC (SDTM and AdaM) standards.

 

CV - PROFILE 106

Lead Consultant, Clinical SAS Programmer Analyst - 25 Years +

A SAS-certified professional with over 25 years’ experience in the clinical reporting industry.  He is very experienced in CDISC standards implementations. He works with SDTM and ADaM, and preparation of tables, listings and graphs. He is a technical manager for all verification projects.  He is instrumental in the review of the verification process along with acting as a verification programmer.   He manages and performs on SAS-based software development projects and data migration projects, and in the preparation of SAS-based clinical study reports in support of NDAs for the pharmaceutical industry.  He provides services in support of SAS/PH-Clinical implementation; SAS Warehouse Administration; SAS/IntrNet implementations and SAS-based clinical reporting environment implementation and migrations.  Specializes in UNIX and Windows platforms