Job Details

Please no third party applicants

SUMMARY:

Join a leading pharmaceutical company as a Senior Statistical Consultant for an engaging 6-month renewable project. We are seeking an experienced professional who is hands-on and adept at supporting regulatory submissions. If you have strong programming skills and expertise in CDISC, we want to hear from you. Exceptional communication skills are essential to effectively convey complex results to the study team.

EXPERIENCE & QUALIFICATIONS

• 8-10+ years of biostatistical experience in the pharmaceutical industry, with a focus on recent Sponsor side roles.
• Minimum of a Master's degree in Biostatistics or Statistics.
• Hands-on experience in drafting SAPs and conducting detailed TLF reviews.
• A proven history of successful regulatory submissions.
• Required ability to analyze datasets and provide strategic guidance to the statistical programming team as necessary.
• Strong communication skills for interpreting and explaining complex analytical results.

LOCATION:

This position is entirely remote, with a preference for candidates who can accommodate PST core working hours.