Sr Statistical Programmer

4 weeks ago

Bengaluru, India Trigent Software - Professional Services Full time
Location:

RemoteExperience:

5+ Years in Statistical ProgrammingImmediate Joiner

Responsibilities:Develop & Validate Programs:

Create and validate statistical programs using

SAS

and/or

R

for clinical trial data analysis.Experience in clinical trial datasets both creation and validation

(e.g., SDTM, ADaM) and

CDISC standards .Data Analysis & Reporting:

Provide programming support for

clinical study reports ,

tables ,

listings , and

figures .Collaborate with Teams:

Work closely with

biostatisticians

to ensure accurate data analysis and timely reporting.Regulatory Compliance:

Ensure adherence to

FDA ,

EMA , and other regulatory guidelines.Documentation:

Assist in the creation and maintenance of

specifications ,

SOPs , and

project documentation .Requirements:5+ Years of Experience

in statistical programming, preferably within clinical trials.Proficiency in SAS and/or R ; experience with other programming languages is a plus.Strong understanding ofExperience in a

CRO

or

pharmaceutical

company is preferred.Excellent Communication Skills

and ability to collaborate in a

global team .

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