Regulatory Affairs Manager - Russian Speaker (home-based)
ソフィア, ブルガリア共和国| ギリシャ共和国| スロバキア (スロバキア共和国)| ルーマニア| ハンガリー共和国| リトアニア共和国| チェコ共和国| エストニア共和国| ポーランド共和国| ブルガリア共和国| Remote
Job Description
To our lifecycle management team we are looking for Regulatory Affairs Manager 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
- Acts as a Regulatory Lead on complex projects, which may include technical writing or may act as a Project Manager for a stand-alone project, with guidance from senior staff as appropriate.
- 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 5 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.iqvia.com
類似職種
-
R1456305
TMF Manager, sponsor-dedicated (Hybrid/home-based, Bulgaria)
複数勤務地詳細はこちら
-
R1458224
Study Coordinator - virtual
複数勤務地詳細はこちら
Join our Global Talent Network
最近情報を配信しています。新しい希望に合った求人がオープンした際にご案内させていただきますので、ご登録ください。