xevmpd Search Results

A Certified Scrum Master (CSM) and people manager with 14 Years of experience in Pharmacovigilance/ Regulatory domain as a techno functional business ... View More

Experienced Regulatory Affairs Manager with expertise in pharmaceutical and medical product licensing, compliance, and marketing. Skilled in project m... View More

Veeva Vault Architect & Enterprise Content Management Professional with 7 years of experience in Veeva Vault (CDOCS, QMS, eTMF/CTMS, MedComms, RIMs), ... View More

With over 15 years of experience in the pharmaceutical industry, I have provided support for regulatory, R&D, quality, and pharmacovigilance functions... View More

Motivated professional with several years of experience juggling multiple priorities to keep company running smoothly. Communicative team leader posse... View More

Regulatory Affairs Professional with 11+ years of experience in regulatory dossier submissions and post approval changes primarily for EU market.

Dynamic regulatory professional with extensive experience at AstraZeneca, specializing in XEVMPD and IDMP submissions. Over 8 years of proven track re... View More

To obtain a challenging a reputed organization like yours, which can provide adequate opportunities and environment position in to enrich my knowledge... View More

Acting as Project manager for IDMP Implementation at Advanz More than 7 years of experience in IDMP domain 9+ years of experience in Regulatory domain... View More

Overall 7.5 years of Regulatory experience including 2.5 years of hands-on experience in Veeva vault data management and enrichment. 5+ years of exper... View More