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Explore Location
Undisclosed
Garden Grove, California, United States
(on-site)
Posted
1 day ago
Undisclosed
Garden Grove, California, United States
(on-site)
Job Type
Full-Time
Min Experience
None
Job Function
Manufacturing
Assistant Site Controller
The insights provided are generated by AI and may contain inaccuracies. Please independently verify any critical information before relying on it.
Assistant Site Controller
The insights provided are generated by AI and may contain inaccuracies. Please independently verify any critical information before relying on it.
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.
Job ID: 84525769
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