ADaM and TFL programming , and deep hands-on experience in
Oncology and/or Immunology efficacy analyses . The ideal candidate will have proven capability in
ADTTE datasets , advanced efficacy endpoints, and generation of complex statistical graphics, along with leadership experience and hands-on
R programming
skills.
This role requires close collaboration with statisticians, data management, and clinical teams to deliver high-quality, regulatory-compliant outputs for Phase II and Phase III clinical studies.
Required Qualifications & Experience
10+ years
of experience in statistical programming within the pharmaceutical, CRO, or biotech industry
Strong expertise in
ADaM and TFL programming
Proven hands-on experience in
Oncology and/or Immunology efficacy analyses
Extensive experience with
ADTTE datasets
and time-to-event analyses
Minimum 2 years of lead or study-level programming experience
At least 1 year of hands-on R programming experience
Solid experience working on
Phase II and Phase III clinical studies
Advanced proficiency in
SAS
(Base, Macros; additional SAS tools as applicable).
📌 Assoc principal Stat Programmer -FSP (Mumbai)
🏢 IQVIA India
📍 Mumbai
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