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Veeva RIMS Sr. Pharma
Career Insights for Regulatory Affairs Manager
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Scorecard
Based on California data
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What they do
A Regulatory Affairs Manager plans, directs, or coordinates production activities of an organization to ensure compliance with regulations and standard operating procedures.
$235,442 / year median in California
-1% projected decline
Job Description
ROLE:
Veeva RIMS - Sr.
Pharma Location:
Foster City, CA ( 4 days onsite )
Duration:
12mo
Status:
w2
Rate Range:
85-95 w2
Domain:
PHARMA Referral:
$ total rate of candidate with referral shouldn t 95hr.
•Must be local to Foster City, CA (Bay area) or nearby cities.
•Only want local
SKILLS MATRIX
YES / NO Years 1-5 Rating
SKILLS REQUIRED
Veeva
RIMS PHARMA
industry exp INDs, NDAs, BLAs, eCTD health authority requirements regulatory affairs, operations
Job Requirements:
Senior Pharma Submission SME with Veeva RIMS 10+ years of experience in regulatory affairs, operations, or technical writing with strong business background within the biotech or pharmaceutical industry Strong experience with Veeva RIMS Expertise in regulatory submissions including INDs, NDAs, BLAs, eCTD, and global health authority requirements Ability to translate complex technical , clinical, and CMC content into compliant submission formats Experience leading submission strategy, process development for authorship, technology leadership , template standardization, process optimization, and audit/compliance support Strong collaboration skills across scientific, regulatory, and publishing teams