Job Title: Statistical Programmer-ll

Location: Hyderabad
Job Type: Full-time
Work Type: Work From Office.
About Us: Sylphid Analytics is a global provider of specialized services to the
pharmaceutical industry, offering high-quality, practical, responsive, and cost-
effective solutions to support biotechnology and pharmaceutical companies. From
Phase I to IV clinical trials, we expedite the development of life-saving drugs and
devices, focusing on adaptability, quality, and efficiency throughout. Our commitment
to excellence ensures that every client experiences complete confidence in our
staff”s knowledge, abilities, and reliability, witnessing clear benefits and results from
our involvement in their projects. By supporting clients who facilitate the acceleration
of drug approvals to market, we contribute to creating a safer and better world,
shaping a brighter future for all.
Responsibilities:
1. Lead and oversee the development, validation, and execution of SAS
programs for statistical analysis and reporting.
2. Collaborate closely with statisticians, data managers, and other cross-
functional teams to ensure the successful execution of clinical trials.
3. Provide expert input on the design and implementation of SDTM and ADaM
datasets, adhering to CDISC standards.
4. Perform quality control activities, ensuring the accuracy and integrity of
statistical output and data deliverables.
5. Contribute to the creation and review of programming documentation,
including programming plans, specifications, and validation documentation.
6. Mentor and guide junior programmers, fostering a collaborative and growth-
oriented team environment.
7. Stay current with industry best practices, emerging technologies, and
regulatory requirements related to statistical programming in clinical research.
Qualifications:
1. Bachelor’s or master’s degree in a relevant field (e.g., Statistics, Computer
Science, Life Sciences).
2. Minimum of 4-7 years of progressive experience as a statistical programmer
in the clinical research industry.
3. Expertise in SAS programming, including advanced data step programming,
macro development, and proficiency with statistical procedures.
4. Strong knowledge of CDISC standards, SDTM, and ADaM datasets and soon
TLF’s.
5. Demonstrated experience in leading programming activities for regulatory
submissions (e.g., FDA, EMA).
6. Excellent understanding of regulatory guidelines such as ICH-GCP and 21
CFR Part 11.
7. Exceptional organizational and communication skills, with the ability to
effectively collaborate in a team environment.
Preferred Skills:
1. Experience with other programming languages (e.g., R, Python) is a plus.
2. Familiarity with data visualization tools (e.g., Spotfire, Tableau).
3. Previous experience with oncology or other therapeutic areas.
How to Apply: Interested candidates are invited to submit their resume,
cover letter, and examples of relevant work here in Apply now. Please include
Senior-Level SAS Programmer Application and in the subject line.