Translator (Regulatory) - Lithuanian Speaker
Job description
Join us on our exciting journey!
Position Purpose:
We are recruiting an awesome new team member to join us at our Madrid Center of Excellence office! This position will provide broad support on monitor and analyze the changes and evolution of the local regulatory environment, including guidance and regulations from regulatory authorities, trade organizations, working groups, and relevant industry thought leaders for both drug and medical devices. y activities and requests.
Responsibilities:
Assess regulatory intelligence information for relevance and impact to industry’s internal processes, drug development projects and/or regulatory strategies to create and enrich the IQVIA proprietary documents.
Monitoring agency and professional websites, local specialized press, conferences and selecting documents to be integrated in line with the IQVIA scope, editorial and intelligence management processes.
Identify business critical aspects and communicate effectively to internal and external stakeholders. This includes regular updates on new information that could impact clinical trial execution, pharmacovigilance activities, manufacturing quality as well as other ad hoc requests.
Synthesize information from regulatory documentation as well as interaction with local country experts as needed.
Share/Input data into systems or tools to enable effective knowledge management of country level operational intelligence data.
Develop and refine regulatory intelligence processes and procedures to build efficiencies
Competency Requirements
Proficiency in MS-Office, Word, Excel, and Outlook
Good organizational skills and ability to meet deadlines working within a time sensitive environment
Detail oriented and the ability to handle multiple priorities while meeting strict deadlines.
Excellent communication and interpersonal skills, with the ability to build strong relationships internally and work within a team environment
Lithuanian and Other Baltics languages and English advanced level are
Capability to work remotely with peers in an international environment.
Good understanding of the drug development and commercialization process
Highly organized and able to work independently to meet deliverable on time and on target
Team-oriented and strong relationship builder, ability to effectively collaborate with a range of individuals across the organization and externally.
Attentive to details and focused on quality output.
Effective communicator - both written and oral - in a multi-discipline team environment
Education, Skills, Experience Desired
Bachelor’s degree or equivalent
2 years or more related work experience
IQVIA™ is an equal opportunity employer. We make employment decisions based on qualifications and merit. We prohibit discrimination based on any unlawful consideration such as age, race, national origin, gender or other "protected status.“
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
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