Job Description
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: or by sending your resume to openings@parexel.com and reference: 000523
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EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
Job Tags
Remote work,
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