SENIOR REGULATORY AFFAIRS SPECIALIST - RUSSIAN SPEAKER (HOME-BASED)

IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients.
Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics, and human ingenuity to drive healthcare forward.
To our lifecycle management team we are looking for Senior Regulatory Affairs Specialist that will support activities on Russian market.
This is an individual contributor role that requires native/fluent Russian language knowledge and solid experience in post approval regulatory affairs in Russia.
Main Responsibilities Competently writes regulatory and technical documents with minimal review by senior staff.
Establishes relationships with customers and stakeholders; may meet face to face without rest of team to discuss regulatory issues and present lessons learned.
Adopts a proactive and flexible approach to resolve any issues.
Undertakes detailed review and management of budgets related to projects, including out of scope activities.
Ensures revenue is recognized and challenges when appropriate.
May give guidance to junior colleagues, including feedback on the quality of technical documents, and may assist in their training and development.
May present to clients at bid defense meetings by phone or in person, for a range of regulatory deliverables, at discretion of senior staff.
May write new regulatory standard operating procedures, and propose revisions or act as reviewer for regulatory standard operating procedures.
Manages meetings with Regulatory Agencies.
Qualifications Bachelor's or Master's Degree Degree in Life Science or related discipline At least 3 years relevant experience in lifecycle management regulatory affairs for Russian market Native (preferred) or fluent in Russian language Good understanding of the Research and Development process (Chemistry, Manufacturing & Controls, Preclinical and Clinical), laws and related guidelines, as appropriate.
Expert in planning and delivering work on time keeping quality parameter in mind.
In depth knowledge of regulatory procedures and intelligence in Russia Ability to work closely with client regional heads to determine the Regulatory, Publishing & submission strategy and execute project plan.
Ability to establish and maintain effective working relationships with coworkers, managers and clients.
Strong software and computer skills, including Microsoft Office, publishing applications and tools, as applicable.
Experience of involvement in regulatory strategy and determination of documentation requirements, timelines, CMC and publishing projects.
Project leadership experience.
Ability to adapt quickly to a rapidly changing environment.
Russian language on level C1 and above #LI-remote IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
Learn more at https://jobs.
qvia.
om IQVIA is a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare – and human health – forward.
Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes.
To get there, it takes diverse skills and a curiosity to explore new possibilities.
No matter your role, everyone at IQVIA contributes to our shared goal of improving human health.
Thank you for your interest in growing your career with us.