Senior Pharma SME with Veeva RIMS

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 shouldnt 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

Title: Director, Regulatory Affairs Location: San Francisco Bay Area (Onsite) Job Description: Reports into Regulatory Affairs, Global Filing & Registration: High-Impact position to lead cross-functional development & regulatory submission activities for registrational oncology programs in the US.Collaborate closely with Program Teams and Global Regulatory Leads to advance effective & consistent regulatory strategies to enable successful filing of approval of New Drug Applications.Develop strate

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. Essential Functions of the Job: Commercial Technology Leadership Lead the operational management of US and JPAC commercial technology platforms supporting Sales, Medical Affairs, Market Access

Primary Function of Position The Sr. Regulatory Affairs primary responsibilities include developing regulatory plans, reviewing design input/output documentation, identification of applicable standards and guidance documents, performing regulatory assessments to determine the impact of design/process changes, preparing regulatory submissions, maintaining regulatory filings and licenses. Essential Job Duties Provide regulatory guidance to product teams, develop regulatory plans, a