Posts Tagged: biostatistical programming company

Senior Statistical Programmer Consultant, San Diego CA

6 month potentially renewable contract, onsite San Diego Responsibilities will include, but are not limited to, the following: • Provide programming input to CRF, SAP, analysis file specifications, and tables, figures, and listings (TFLs) shells. • Write SAS programs to generate derived analysis datasets, perform analysis, and TFLs. • Perform ad hoc flexible and rapid… Read more »

Senior Statistical Programmer; Direct Hire – San Diego, CA

The Senior Statistical Programmer will lead statistical programming support to major clinical studies, including ad hoc analysis for clinical development, drug safety, regulatory affair, medical affair, and research group. He/she will be working with CROs to ensure projects meet agree upon timeline with good quality, developing ISS/ISE, converting legacy study data to CDISC for submission,… Read more »

Director of Data Management; San Diego, CA

We are seeking a leader to head the DM team in overseeing several ongoing trials, starting-up new trials and providing DM vendor oversight activities across the development programs. The incumbent will work closely with the head of Biometrics in identifying project DM demands and resource needs. Provides hands-on support to project teams by leading data… Read more »

Senior Data Manager; San Diego, CA

  We are seeking a Data Manager with a keen attention to detail who will be responsible for overseeing the start-up and execution of several trials with a CRO and additional support with upcoming submissions. The individual will coordinate and manage daily data management and vendor oversight activities for multiple clinical trials to support both… Read more »

Seattle Contract Statistician

Onsite Seattle preferred but will consider remote for ideal candidate W2 Only – 6 month contract Responsible for statistical aspects of clinical and pre-clinical research projects including study design, sample size estimation, patient randomization, case report form development, writing statistical analysis plans, statistical analysis and interpretation of data, and reporting of results. Work with SAS… Read more »

Leading CRO hiring multiple permanent Senior or Principal Biostatisticians, onsite or remote thru United States

Principal Biostatistician Overview: Designs, plans, and executes biostatistical components of clinical trials. Uses sound statistical methodology to conduct studies, prepares the statistical components of protocols, and is responsible for the statistical components of reports. Responsibilities:  Serves as the lead biostatistician on programs of studies or submissions, or on simple to complex individual studies. •    Serves… Read more »

More Efficiency, More Talent + More Value in 2017

Another year is upon us, and here at SimulStat we’re focusing 2017 on more ways to provide added value to our clients. With more efficient processes in place and a bigger talent pool of data managers, SAS programmers, biostatisticians and epidemiologists to pull from, we’re adding more value to our core services. Here’s a closer… Read more »

Staff Spotlight: Tristan Gittens, Senior SAS Programmer at SimulStat

Meet Tristan Gittens, our Senior SAS Programmer. With a background in Pre-Med at UC Berkeley, a Masters of Science in Epidemiology at Stanford University, and a substantial amount work experience in the field of science, Tristan is an extremely valuable member of our team who brings a wealth and variety of knowledge. In his current… Read more »

It’s going to be a BIG year for Biostatisticians and Statistical Programmers

As we look back on another successful year at SimulStat, we can’t help but make some predictions about the coming year. Throughout 2015, we saw an extremely high demand for contract biostatisticians and statistical programmers. Much of this demand came from pharmaceutical and biotech companies looking to bring some of their biostatistics/statistical programming in-house versus… Read more »