Offer summary

Qualifications:

Master's Degree in Medical Statistics or a related field., At least 5 years of experience in biostatistics roles., Experience leading multidisciplinary study interactions across time zones., Proficiency in developing and QC of SAS or R programs and statistical reports..

Key responsibilities:

Provide statistical support for trial designs, protocols, and CRF development.

Lead production and quality control of analysis plans, reports, and documentation.

Perform sample-size calculations, generate randomization lists, and write statistical methodology sections.

Mentor junior biostatisticians and collaborate on SDTM & ADAM specifications.

Job description

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

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

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.

Required profile