Job opportunity
Senior Statistical Analyst II
Tigermed
Responsibilities
Develop and validate complex
analysis datasets (ADaM)
and
TFLs
using SAS.
Write and review
programming specifications
and supporting documentation.
Create
standard macros
and tools to improve efficiency.
Serve as a
project lead programmer , assigning tasks, managing timelines, and providing technical guidance to junior team members.
Communicate with clients as the
key programming contact , including delivering outputs and managing feedback.
Conduct
SAS code review , track issues, and ensure quality standards are met.
Archive all programming deliverables and documentation per SOPs.
Mentor team members and support their technical and professional development.
Ensure compliance with
ICH-GCP , CDISC standards, and company SOPs.
Requirements
Bachelor's degree or above
in Statistics, Mathematics, Computer Science, or related field.
5+ years of SAS programming experience
in pharmaceutical or CRO environments.
Strong knowledge of
clinical trials ,
statistical methods , and
regulatory requirements .
Proven experience
leading programming projects
and mentoring team members.
Excellent
communication skills
and experience working with global teams and clients.
#J-18808-Ljbffr
Apply on source site Develop and validate complex
analysis datasets (ADaM)
and
TFLs
using SAS.
Write and review
programming specifications
and supporting documentation.
Create
standard macros
and tools to improve efficiency.
Serve as a
project lead programmer , assigning tasks, managing timelines, and providing technical guidance to junior team members.
Communicate with clients as the
key programming contact , including delivering outputs and managing feedback.
Conduct
SAS code review , track issues, and ensure quality standards are met.
Archive all programming deliverables and documentation per SOPs.
Mentor team members and support their technical and professional development.
Ensure compliance with
ICH-GCP , CDISC standards, and company SOPs.
Requirements
Bachelor's degree or above
in Statistics, Mathematics, Computer Science, or related field.
5+ years of SAS programming experience
in pharmaceutical or CRO environments.
Strong knowledge of
clinical trials ,
statistical methods , and
regulatory requirements .
Proven experience
leading programming projects
and mentoring team members.
Excellent
communication skills
and experience working with global teams and clients.
#J-18808-Ljbffr