Website:
mentriix.com
Job details:
Company Description
Mentriix, operating under High Standards Inc, is a global Clinical Research Organization (CRO) specializing in comprehensive solutions across the clinical trial lifecycle. With expertise in Clinical Data Management, Clinical SAS Programming, Biostatistics, and Statistical Programming, Mentriix supports Oncology and Non-Oncology clinical trials. The company implements CDISC standards and provides regulatory submissions support across agencies like FDA, EMA, and PMDA. Mentriix has a global presence, with operations in India, the USA, and South Africa, and partners with Pharma, Biotech, and CROs to deliver compliant and cost-effective research solutions.
Role Description
This is a full-time remote role for a Principal SAS Programmer with expertise in R and Oncology. Responsibilities include developing and validating complex statistical programs, ensuring compliance with industry standards like CDISC, and analyzing clinical trial data. The role also involves collaborating with biostatistics, data management, and regulatory teams to create datasets, tables, listings, and figures (TFLs) for oncology studies. Additionally, the role requires implementing advanced analytics and ensuring seamless communication of programming outputs to stakeholders.
Qualifications
- Strong expertise in Statistical Programming and proficiency in SAS and R programming
- Advanced Analytical Skills to interpret clinical data and generate statistical insights
- Experience in Data Management and handling datasets such as SDTM and ADaM
- Proficiency in Statistics and familiarity with oncology-specific trial methodologies
- Excellent understanding of CDISC standards and regulatory requirements for clinical trial programming
- Strong problem-solving and communication skills to collaborate effectively in cross-functional teams
- Background in Oncology trials is highly beneficial
- Master's or Bachelor's degree in Biostatistics, Computer Science, or a related discipline
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