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Assistant Site Controller

Job

Confidential

Garden Grove, CA (In Person)

$164,984 Salary, Full-Time

Posted 1 week ago (Updated 14 hours ago) • Actively hiring

Expires 7/6/2026

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Job Description

Assistant Site Controller at Confidential Assistant Site Controller at Confidential in Garden Grove, California Posted in 1 day ago.
Job Description:
Senior Statistical Analyst (Eye Care | Aesthetics), AbbVie Inc.,
Irvine, CA:
Hybrid (onsite 3 days a week/ 2 days WFH). Deliver statistical programming expertise for clinical studies with lower complexity. Ensure accurate data analysis, reporting, & adherence to regulatory standards. Develop SAS programs for generating ADaM datasets, tables, listings, & figures. Create specifications for ADaM datasets for individual & integrated analyses. Collaborate closely with crossfunctional teams to achieve project objectives. Prepare documentation for regulatory submissions, including reviewers guides & data definition documents. Lead development of standard SAS macros & participate in development of standard operating procedures. Provide supervision & mentorship to statistical programmers & analysts. Must have a MS in statistics, biostatistics, computer science, mechanical engineering or a related field & 2 years as a statistical analyst leading statistical programming activities for clinical studies. Of experience required, must have 2 years: (i) applying SAS programming concepts & techniques related to drug development; (ii) creating & validating ADaM datasets in compliance with CDISC/ADaM Standards; (iii) providing statistical programming supporting for Phase
I, II, & III
clinical trials; (iv) generating clinical outputs (tables, listings, & figures) with SAS; & (v) utilizing each of the following SAS tools:
SAS/BASE, SAS/MACROS, SAS/SQL, SAS/GRAPH, & SAS/STAT.
Alternatively, would accept a BS in statistics, biostatistics, Computer science, mechanical engineering or a related field & 5 years as a statistical analyst leading statistical programming activities for clinical studies. Of experience required, must have 5 years: (i) applying SAS programming concepts & techniques related to drug development; (ii) creating & validating ADaM datasets in compliance with CDISC/ADaM Standards; (iii) providing statistical programming supporting for Phase
I, II, & III
clinical trials; (iv) generating clinical outputs (tables, listings, & figures) with SAS; & (v) utilizing each of the following SAS tools:
SAS/BASE, SAS/MACROS, SAS/SQL, SAS/GRAPH, & SAS/STAT.
Work experience may be gained concurrently. Will accept reasonable combination of education, training & experience.
Salary Range:
$146,467.84 - $183,500.00 per year.
Apply online at https:
//careers.abbvie.com/en or send resume to Job.opportunity.abbvie@abbvie.com. Refer to
Req ID:
REF49786C.
recblid p8flj05ftu6wvxe4o7yqpvyqws69or