Plc programming serp_jobs.h1.location_city
serp_jobs.job_alerts.create_a_job
Plc programming • pasadena ca
- serp_jobs.job_card.promoted
Biostatistical Programming Manager
VirtualVocationsPasadena, California, United StatesPLC Controls Engineer
Toni GroupLos Angeles, CA, USProgramming Insights Associate
Disney Direct to ConsumerGlendale, California, United StatesPLC Controls Engineer
Career Search AssociatesLos Angeles, CAPLC Controls Engineer
Career Development PartnersLos Angeles, CA- serp_jobs.job_card.promoted
CMM Programming Manager
Hadrian AutomationLos Angeles, CA, USProgramming Manager, Orchestral
LA PhilLos Angeles, CAPLC Controls Engineer
OneSource Technical, IncLos Angeles, CAPLC Controls Engineer
Professional Recruiting Consultants, Inc.Los Angeles , CAPLC Controls Engineer
Lordan AssociatesLos Angeles, CAProgramming Manager, Orchestral
Hollywood BowlLos Angeles, CA- serp_jobs.job_card.promoted
Manager, Statistical Programming
Arrowhead PharmaceuticalsPasadena, CA, USCoordinator, Music Programming
Sirius XMLos Angeles, California, USPLC Controls Engineer
bizjobz LLCLos Angeles, CAProgramming Manager, Orchestral
Los Angeles Philharmonic AssociationLos Angeles, CA, USAPLC Controls Engineer
Integra PersonnelLos Angeles, CAPLC Controls Engineer
The Recruiting ProLos Angeles, CAtutor - Java programming
BUKILos Angeles, CA, USPLC Controls Engineer
Retail OptionsLos Angeles, CAPLC Controls Engineer
Career Professionals, IncLos Angeles, CABiostatistical Programming Manager
VirtualVocationsPasadena, California, United States- serp_jobs.job_card.full_time
A company is looking for a Biostatistical Programming Manager to oversee statistical aspects of clinical activities. Key Responsibilities Oversee the execution and quality of projects managed by Functional Service Providers (FSPs) according to quality oversight plans Align FSP assignments with development priorities and ensure compliance with quality and timeline expectations Provide technical consultancy and guidance to FSP staff on processes, tools, and utilities Required Qualifications Doctorate degree OR Master's degree with 2 years of experience OR Bachelor's degree with 4 years of experience OR Associate's degree with 8 years of experience OR High school diploma / GED with 10 years of experience in statistical programming Master's in Computer Science, Statistics, Mathematics, Life Sciences, or a relevant scientific subject preferred Experience in regulatory submissions and vendor / resource management In-depth knowledge of SAS / Graph and Stat packages 6+ years of statistical programming experience in the biopharmaceutical industry