Regulatory Affairs Lead CIS

компания "teva" key accountabilities: develop regulatory strategies and implementation plans for new products analyze ra status in the region, identify emergencies/gaps and propose/implement improvements follow working plan (timely submissions/approvals) and ensure smooth ra operations: maintain database for approved ra documents. timely utilize the company software: prepare for, patriciate in calls and provide accurate ra input on regular basis at meetings and forums at local and global level: build and maintain effective communication with cis market ra, sc, commercial, qa, pv, medical, portfolio, ru ra team, mnf sites and mahs keep up to date with local market requirements – timely communicate and implement changes find ra solutions for entering new markets - researched and provide regulatory intelligence to business by reviewing and evaluating ra requirements and submission strategy, including working with third-party agents requirements: high education diploma in medicine or pharmacy from 3 years of experience in regulatory affairs gained with pharmaceutical industry or agency experience of work with cis markets is mandatory understanding of the commercial implications of the business very good people management skills developed verbal and communication skills, including presentation and coaching/training skills high level of accuracy, attention to details, ability to work with big volume of data and meet deadlines computer literacy good english skills