Work as a statistician on clinical trials; producing and validating complex outputs to excellent quality whilst adhering to deliverable timelines. Producing and reviewing Statistical Analysis Plans (SAPs), protocols and other pertinent study documentation. Acting as lead statistician within a reporting team environment, being responsible for statistical aspects of reporting out study results. Working as a global lead statistician across multiple studies, overseeing more junior leads and supporting regulatory interactions. Preparing randomisation schedules and acting as the unblinded statistician on reporting teams. Acting as a statistical consultant to pharmaceutical or biotech companies. Excellent team work ethos, and willingness to help others. Potential to have line management responsibilities.
This position is full-time and fully-remote. The successful candidate may be based in India.
Responsibilities
The following areas of expertise will be aligned to the role...
Statistical expertise and scientific leadership
Leadership and people development
Compliance, quality and governance
Communication and influence
Qualifications
PhD or MSc in Biostatistics or a related discipline
At least 5 years of relevant pharmaceutical industry experience
The ability to write post-hoc analysis plans, allowing internal programmers to do the formal programming of the required outputs/analysis
Robust SAS programming skills for SAS/BASE, SAS/STAT, SAS/GRAPH and ODS functionality
CDISC knowledge (SDTM and ADaM)
Study lead experience
The ability to work on complex efficacy is advantageous
Why Join Us
Remote working and flexible working hours
Career development, mentorship, and continuous learning
Supportive, friendly, and collaborative culture
About Phastar
Phastar is an award-winning biometrics and data science CRO, trusted by pharma, biotech, and medical device companies worldwide. With a global team of data specialists, we bring expertise, precision, and pace to every trial, be
📌 Senior Statistician (India)
🏢 PHASTAR
📍 India
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