Sr. Biostats Location:Â
Mumbai, Pune, Ahmedabad, Bangalore, Chennai, Hyderabad, Kochi, Gurgaon
Mandate Skills:Â
Thorough understanding of statistical principles and study design methodology; should have worked on clinical trials phase 1-4
...
• 6-8+ yrs of statistical programming (production/validation) experience using base sas, advanced sas in CRO/Pharma space • Min 6 years in CDISC SDTM, ADaM and TLFs programming
• Experienced with developing mapping specifications for SDTM and ADa...
Company Description Clinovo is an ISO certified global service partner for pharmaceutical, biotechnology and medical devices companies. We specialize in delivering excellence on the clinical development value chain to improve the quality of life fo...
Minimum qualifications:
~ Bachelor's degree or equivalent practical experience.
~3 years of experience working with statistical packages (e.g., R, SAS, Stata, MATLAB, etc.).
~ Experience in articulating product questions, pulling data from da...
...Statistical programmer will responsible for statistical programing for clinical trial studies. Programmer will develop and validate SAS programs for datasets, and outputs (TLFs).Looking for well experienced candidat...
...communication, negotiation, and interpersonal skills.
Willingness to travel as needed to meet with SAs and attend industry events.
Ideal... ...for managing and growing the network of Di...
...Job Description
TCS is hiring for Senior Clinical Statistical Programmer
Work Location - Hyderabad/Noida
Experience Range - 5 to 12 Years
Educational Qualification(s) Required- Graduate/Post Graduate...
...and figures
Coordinate programming activities among the study programmers to achieve timely deliveries
Access and convert data to SAS... ...Educational requirements:
~ Bachelors degre...
...CRO activity, run post-hoc analysis, etc.,
~ Must have experience writing SOPs for biostatistics
~ Experience with ophthalmic gene therapy is a plus, but not required.
About Us:
Inductive Quotient An...
