Provide expert guidance and tailored solutions on projects, programs, and processes that span multiple related areas in support of the organization's overall Clinical Data Standards strategy
Job Summary
Provide expert guidance and tailored solutions on projects, programs, and processes that span multiple related areas in support of the organization's overall Clinical Data Standards strategy.
Responsible for the development and maintenance of clear specifications for standard content across the data lifecycle, including data collection, delivery, analysis & reporting, aligned with program requirements and medical writing.
We offer a competitive salary and extensive benefits package, a flexible working environment, and career development opportunities.
Matching Summary
Provide expert guidance and tailored solutions on projects, programs, and processes that span multiple related areas in support of the organization's overall Clinical Data Standards strategy.
Skills & Requirements
Must-have
Clinical Data Standards
CDISC standards
ICH GCP regulatory requirements
data collection and analysis tools
SAS programming
Nice-to-have
customer focus
solution-oriented
interpersonal skills
cross-functional leadership
decision making and problem solving
Key Requirements
Bachelor’s degree in scientific, technology or healthcare discipline
At least 6 years of relevant pharmaceutical/scientific experience