We are looking for Senior Content Editor Regulatory Intelligence to join our team in Barcelona on a Fix Term Contract.You’ll join our Life Sciences Regulatory team that provide far more than just content sets. . Our data are enriched with unique abstracts, commentaries and analysis prepared by our team of industry experts — critical insight on-tap from the thought leaders that shape pharmaceutical opinion. All over the world, decision-makers depend on us for the essential knowledge that can justify their strategies, promote outstanding research and business growth, and keep them abreast of the market.About You – experience, education, skills, and accomplishments Degree in Sciences (Pharmacy, Pharmacology, Biology, Chemistry, Biomedical Sciences, etc.) or equivalent experience4+ years’ experience in pharmaceutical sector with knowledge of regulatory landscape and procedures within country/region.Excellent written and oral communication skills in English.Drug development lifecycle knowledge.Hands on experience of being engaged in clinical research (in pharma or CRO) or regulatory documentation or PV compliance activities.It would be great if you also had . . .Demonstrated ability to work collaboratively in a highly matrixed organization.Good skills of problem-solving and good judgment in decision making and setting priorities.Capability to work remotely with peers in an international environment.Versatile in a multitasking environment.Analysis of large volumes of structured or unstructured data.Ability to delve deep into content and results.Additional language skill such as French, Arabic represents an asset.What will you be doing in this role? You’ll work on Regulatory surveillance, Maintenance of regulatory content for a given set of countries and Customers support:Ensure the contents of CRI proprietary documents are valid and updated for the assigned countries by assessing impact of drug/devices changing regulations.Collaborate with a pool of external consultants: undertake the research and identification of local experts, negotiating contract terms, managing budgets of maintenance.Coordinate cross countries validation of content par thematic criteria.Perform in depth analyses of changes impacting the current regulatory compliance for the pharmaceutical industry.Handle internal and external customer queries to fulfil their needs.Provide customer support and expertise; communicate the enriched regulatory content to sales or product specialists.Management of vendors: scope of work for local consultants and other service providers where applicable, copyrights and invoice management.Management of editorial procedure and rules: strategic discussion, documentation.About the Team You’ll be reporting to the Senior Team Manager, based in France.We are an international and diverse team of more than 10 colleagues based around the world.The team culture is dynamic, creative, and supportive – excellence, integrity, and care are in our DNA.You’ll have 40 annual paid hours of volunteering time and the chance of being part of an active volunteering community which promotes diversity and inclusion across the business.Hours of WorkThis role 40 horus per week in Barcelona, EU hours, and we offer a Fix Term Contract until 1 April 2024. Hybrid, going to our central office 2-3 times per week.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.
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