Provide broad statistical support for trial designs, protocols & CRF development on specific studies; Lead production & quality control of randomization, analysis plans, statistical reports, statistical sections of integrated clinical reports & other process supporting documents; and Perform sample-size calculations, generate randomization lists & write statistical methodology sections for inclusion in study protocols.
Must have a Master's Degree in Medical Statistics or a related field, and 5 years of experience with each of the following:
(i) Leading interactions w/multidisciplinary study across different time-zones;
(ii) Contributing to planning & delivery of core documents, such as Clinical Study Report, Statistical Analysis Plan & publications;
(iii) Collaborating on SDTM & ADAM specifications & quality control;
(iv) Developing & QC SAS or R programs & across, tables, listings & figures as specified in the SAP; and
(v) Mentoring junior biostatisticians.
Experience may be gained concurrently. 100% Telecommuting permitted from within the United States. Pay rate: $165,000. Apply online at: https://jobs.parexel.com/en/search-jobs or by sending your resume to openings@parexel.com and reference: 000523
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