Associate Content Editor Drug Safety Intelligence Job In Clarivate In Hyderabad / Secunderabad, Telangana, India

We are looking for an Associate Content Editor to join our team in Hyderabad This is an amazing opportunity to work on OFF-X, a translational drug safety intelligence portal The team consists of 20 people located in Spain and India and is reporting to the Regulatory and drug safety manager line We have a great skill set in the analysis of drug safety and toxicity data and we would love to speak with you if you have skills in pharmacovigilance and summary of data About You - experience, education, skills, and accomplishments .

At least 1 year of experience in pharmacovigilance and/or in editorial teams focused on scientific publicationsProven knowledge of basic pharmacology and drug safety An advanced level of English is also requiredMS or PhD in pharmacology, toxicology, biochemistry, biotechnology, medicinal chemistry or a related biological science.

Excellent interpersonal, organizational skills and teamwork skillsIt would be great if you also had Familiarity with databases and scientific information systems.

Experience on writing regulatory documentation or scientific publicationsWhat will you be doing in this roleAnalysis and interpretation of published data (clinical trials, journal articles, reviews, meta-analysis, congress communications, drug approval reports, etc)Collection and curation of information on risks and safety of drug products (recording, archiving, updating and evaluating the information)Writing case studies, reports and reviews.

Maintain informed discussions with experts and customersAbout the Team Our editorial team is a group of 20 people creating and delivering content for OFF-X, a translational drug safety intelligence portal that allows user to easily identify new safety liabilities We are a global team based on India and Spain with more than 50 years of experience in the sector We create and classify content for more than 300 references every week, including Journals, Congress publications and Regulatory documents In this team you will have the opportunity to be up-to-date with all the new advances in the drug development industry and you will be constantly learning new things.

Hours of Work General Shift - 9 AM to 6 PM ISTWe offer a full-time (40 hours/week) (Monday to Friday)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

Clarivate is looking for Phd.

Clarivate is looking for Phd profile candidates.