Location: Home-Based Anywhere in North America
Closing Date: 06 May 17
Type: Full Time
Salary (£): Negotiable
We are seeking Biostatisticians to analyze all parts of any clinical study, and provide planning on multiple clinical studies from multiple clients including tracking project activities and project time management.
Principal Biostatistician, Biostatistics* *These remote opportunities are open to any North America home-office location. We are seeking Biostatisticians to analyze all parts of any clinical study, and provide planning on multiple clinical studies from multiple clients including tracking project activities and project time management. In this role, the selected candidate will prepare/review ISS/ISE statistical analysis plan; review/prepare patient evaluability listings; review protocol and CRF, data management plan and edit specifications; request and perform breaking of blind procedure; prepare/review interim and statistical analysis plan; prepare and review data display and annotation of safety and efficacy shell data displays; perform quality control of complex safety, efficacy, ISS, ISE data displays as well as data integration; provide specifications and review for structure, content and algorithms for ADaM efficacy datasets; prepare statistical report and statistical section of CSR; prepare charter for DSMB/DMC. We require a Master’s degree/Ph.D. in statistics/Biostatistics or equivalent; at least 7 years for M.S. or at least 4 years for Ph.D. in clinical statistics experience along with at least 1 year of managing people/projects and understanding of ICH Guidelines E3, E9, E10. High degree of accuracy and attention to detail along with proficiency in SAS and ability to program using SAS macro language required. Proficiency in statistical procedures including non-parametric analysis, linear and non-linear models, categorical data and survival analysis techniques and understanding of data management flow in a clinical trials environment is also required along with excellent project management and organizational skills. For more information: www.Chiltern.com At Chiltern, you'll join a team of like-minded individuals headed by some of the most dynamic and influential leaders in drug and medical device development today. You'll work on cutting-edge global research projects in a fast-paced but collegial atmosphere where you'll have the opportunity to make meaningful - and acknowledged - contributions. You'll have opportunities to grow personally and professionally and abundant room for advancement along with generous incentive programs. Chiltern is the leading, global mid-sized contract research organization that listens to client needs to deliver customized clinical development solutions. Chiltern’s team of more than 3,700 works across 47 countries to provide flexible, specialized services, with core competencies in Biopharma, Medical Device and Diagnostics, Oncology, Clinical Analytics and Source. Visit Chiltern.com to learn more about responsive solutions that are Designed Around You®... Chiltern is an EEO / AA Employer and is committed to providing opportunities to minorities, women, individuals with disabilities and veterans.
1016 W 9th Ave, King of Prussia, United States
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