Content Editor - Regulatory Intelligence

We are looking for a Content Editor to join our Regulatory Intelligence team in Belgrade. This is an amazing opportunity to learn more about the IP & regulatory intelligence in general. You would be reporting to the Senior Team Manager of Contend Editing. We would love to speak with you if you're enthusiastic person with life sciences background, and ideally have previous experience in the field of regulatory intelligence.About You – experience, education, skills, and accomplishments Bachelor’s degree (Pharmacy, Chemistry or similar)Advanced level of English languageIt would be great if you also had . . . 2-4 years’ experience in pharmaceutical sector and/or regulatory affairs departments.Another European languageDemonstrated ability to work collaboratively in a highly matrixed organizationGood communication skills and proactivityExperience with analysis of large volumes of structured or unstructured dataWhat will you be doing in this role?Monitor the evolution of regulatory landscape worldwide (Monitoring of Regulatory information on the Agency and/or Governmental website)Analyze the changes in the regulatory requirements and implement them in the databases.Work in collaboration with a pool of external consultants: undertake the research and identification of local experts, negotiating contract terms, managing invoices and copyrights when needed.Provide transversal support to the team and the organization on aspects related to candidate subject matter expertiseCommunicate relevant information to concerned stakeholders, internal and customer facing; undertake any other reasonable duties as requested by the line manager on a permanent or temporary basisAbout the Team Regulatory Intelligence information is part of the Clarivate LS Content Operations Group and comprises several teams responsible for the daily collection, synthesis and maintenance of data relating to regulatory information. These records form a core element of our Cortellis RI database.The Content Editor is responsible for providing accurate and timely regulatory intelligence information for specific set of countries & for the monitoring of the information from identified sources in line with CRI scope and editorial processes, providing in depth analyses of changes impacting processes and submissions for the pharmaceutical industry. Within the team, the candidate will participate to the elaboration and development of the regulatory content for the Country modules assigned.Hours of Work Standard Serbian working hours, full-time employment. #LI-HybridWe Offer:Private health insurancePaid lunchYearly bonusYearly merit planMy Learning platformFamily benefits: Bushido kids sports school, tutorship lessonsFitPassMental health care - Psychotherapy sessionsCompany bicycles for rent free of charge25 days of annual leaveOnly shortlisted candidates will be contacted.At Clarivate, we are committed to providing equal employment opportunities for all persons with respect to hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. We comply with applicable laws and regulations governing non-discrimination in all locations.