Principal Biostatistician

At Emerald Clinical, we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We are dedicated to advancing clinical research through scientific expertise and operational excellence, supporting biopharmaceutical, medical device, and diagnostic customers across all trial phases, from registration to post-marketing.

Our therapeutic expertise spans renal, cardiometabolic, and oncology—areas where we make a significant impact on improving global health.

At the heart of our success is our ability to combine global reach with local knowledge. Our on-the-ground teams work closely with local communities, building trust and ensuring diverse, representative patient recruitment. By prioritizing people, we deliver better engagement, more accurate data, and faster results—bringing therapies to patients in need.

Why Join Us

At our core, Emerald Clinical is committed to transforming clinical research by putting people first—both patients and our employees. By joining our team, you'll be part of a global network of passionate professionals working together to deliver better research and outcomes for millions worldwide.

Here's what makes us stand out :

• Purpose-Driven Work : You'll contribute to clinical trials that genuinely improve lives, with a focus on therapies in renal, cardiometabolic, and oncology.
• Global Reach, Local Expertise : Our teams connect with local communities, building trust and meaningful engagement for every trial.
• Collaboration and Innovation : Work in a culture that values diverse perspectives and creative solutions to solve global health challenges.

About the Role

The Principal Biostatistician is responsible for Emerald Clinical projects by performing statistical programming and biostats activities as directed by senior management or statistical services lead at Emerald Clinical.

Your Responsibilities

o Participate as biostatistician on project(s) including but not limited to reviewing protocols, preparing analysis plans, randomization plan, and writing sections of joint clinical / statistical reports.

o The programming, testing, and documentation of statistical programs for use in creating statistical tables, figures and listings. o Giving inputs to protocol writing for stats section and sample size estimation and power calculations. o Programming SDTM datasets.

o Programming analysis datasets (derived datasets including efficacy datasets) and transfer files for internal and external clients.

o The programming quality control checks for the source data and report the data issues periodically o Participating in DSMC / DSMB o Answering queries from regulatory authorities.

Training, Quality and Compliance

Customer Focus and Teamwork

meetings and activities as required

organization

Work Health and Safety

with established organisational WH&S practice and procedures

Education and Experience

Biostatistics or related work in the CRO environment

Competencies

and ambiguous environments

What We Offer

We understand that great work happens when people feel valued and supported. That's why we provide :

Interested Apply now and help us achieve our mission to improve the health of millions worldwide.

Skills Required

statistical programming, biostatistics , Sas, Microsoft Office