Location: Hyderabad

Salary: As per the Market standard

Roles & Responsibility

• Perform Biostatistics activities in accordance with corporate quality standards, SOPs/Work Instructions/Guidelines, ICH-GCP and/or other regulatory requirements.
• Analyze clinical trial data producing accurate results representing the outcome of the trial. Validates statistical output.
• Provide input into statistical standard operating procedures (SOPs) and general standardization efforts within the department (e.g., statistical methodology standards, standard data presentations).
• Participate in interactions with regulatory agencies, as required

Preferred Technical And Professional Expertise

• Good Knowledge in ICH-GCP(E6), ICH-E9.
• Knowledge in BASE SAS, SAS.
• Working knowledge in CDISC Standards like SDTM, ADaM and other Regulatory guidelines.

Good To Have

• Communication skills – effective and amicable communication between groups, developers testers, designers, and users.
• Analytical skills – Good understanding of algorithms and logic that goes behind coding the application.
• Collaboration and team-orientation.
• Creativity, originality, and out of the box thinking capability.

Qualifications

• Bachelor’s or Master’s degree in Biostatistics, Statistics, Life Sciences, Pharmacology, Bioinformatics or a related field.

Why Inductive Quotient? We are team a of 75 + talented and passionate professionals with strong statistical and analytical

background combined with required study expertise.

We take lots of pride in our culture that enables open and creative thinking, deeply valuing us

employees and their contributions towards our organization success.

Skills: base sas,ich-gcp,sas