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Programming • fullerton ca
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Remote Statistical Programming Director
VirtualVocationsWhittier, California, United StatesWell-being Programming Assistant
Chapman UniversityOrange, CA, USThe average salary range is between $ 61,034 and $ 72,670 year , with the average salary hovering around $ 63,504 year .
- traffic engineer (from $ 94,459 to $ 208,000 year)
- material engineer (from $ 114,920 to $ 199,680 year)
- clinical pharmacist (from $ 190,996 to $ 192,787 year)
- pharmacist (from $ 50,113 to $ 191,821 year)
- firmware engineer (from $ 95,000 to $ 191,000 year)
- dentist (from $ 28,600 to $ 175,000 year)
- senior (from $ 59,226 to $ 174,000 year)
- senior software engineer (from $ 118,000 to $ 174,000 year)
- Stamford, CT (from $ 146,419 to $ 229,550 year)
- Hayward, CA (from $ 105,650 to $ 215,000 year)
- Santa Clara, CA (from $ 80,196 to $ 186,000 year)
- Santa Clarita, CA (from $ 80,196 to $ 186,000 year)
- San Francisco, CA (from $ 68,319 to $ 186,000 year)
- San Jose, CA (from $ 61,186 to $ 185,044 year)
- Philadelphia, PA (from $ 95,000 to $ 185,000 year)
- San Mateo, CA (from $ 60,217 to $ 185,000 year)
- San Antonio, TX (from $ 61,779 to $ 184,770 year)
- San Diego, CA (from $ 65,001 to $ 183,869 year)
The average salary range is between $ 46,226 and $ 136,493 year , with the average salary hovering around $ 72,061 year .
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Remote Statistical Programming Director
VirtualVocationsWhittier, California, United States- Full-time
- Remote
A company is looking for an Associate Director, Statistical Programming (Remote).
Key Responsibilities
Lead statistical programming teams and support the development, regulatory approval, and market acceptance of products
Design, develop, and implement technical solutions for integrating, analyzing, and reporting clinical data
Validate programming results from external vendors and independently develop, validate, troubleshoot, and maintain complex programs
Required Qualifications
Bachelor's degree with 12 years, Master's degree with 8 years, or PhD with 5 years of experience in Biostatistics or Statistics
At least 8 years of programming experience in the industry, including support of significant regulatory filings
Proficient knowledge of drug development processes, clinical trial methodology, and regulatory guidance
SAS programming experience in oncology studies
In-depth understanding of clinical data structure and relational databases