Statistical programming for drug development programs
Cross-functional collaboration within and outside aqs
Sas/r programming expertise with advanced macros
The Associate Director ensures efficient execution of trial/program level plans, delivering high-quality results on time
Job Summary
The Associate Director ensures efficient execution of trial/program level plans, delivering high-quality results on time.
They are responsible for allocating resources within a program and ensuring resource sharing to meet organizational goals.
This role requires a thorough understanding of the drug development process, experience in regulatory activities, and expertise in statistical reporting.
Matching Summary
The Associate Director ensures efficient execution of trial/program level plans, delivering high-quality results on time.
Skills & Requirements
Must-have
Statistical programming for drug development programs
Cross-functional collaboration within and outside AQS
SAS/R programming expertise with advanced MACROs
CDISC, eCTD, Define.xml industry standards
Early development experience in Oncology
Leadership and people management of programmers
Nice-to-have
Experience in Immunology, Cardiovascular & Metabolic Diseases
Experience in Neuroscience therapeutic areas
Represent SP in audits and Health Authority meetings
Key Requirements
BS/MS degree in life science, computer science, statistics, mathematics, or equivalent
Fluent in English
Early development experience
Matrix or people management of approximately 6-15 programmers