Associate Content Editor - Pharmacokinetics

We are looking for an Associate Content Editor to join our DMPK team in Chennai/Bangalore. This is an amazing opportunity to work on DMPK knowledge area of Cortellis Drug Discovery Intelligence (CDDI). This is a great opportunity to collaborate with a talented team of experts placed in Barcelona, Chennai, Hyderabad and Bangalore. We have a great skill set in Life sciences and we would love to speak with you if you have the skillset in fetching relevant content from scientific sources like journals, patents, congress abstracts and FDA documents on drug pharmacokinetics, and drug-drug interactions content. About You – experience, education, skills, and accomplishments 1-3 years work experience in Pharmacokinetics or Drug-Drug interactions fields of work is requiredProven experience in analyzing and extracting relevant data from scientific sources related to Pharmacokinetics content Education (B.Pharm / M.Pharm / Pharm.D (Pharmaceutics/Pharmacology)Strong collaboration, motivation, and communication skills with the ability to interact effectively with other team members in different geographiesAbility to deal with ambiguity and changing prioritiesAbility to work according to established service level agreements with end customersTechnical skills as defined for technology areaA good team player with the ability to work on own initiativeWell organized and disciplined with regards policy, procedure, and standards It would be great if you also had . . .  A PhD or postgraduate background in pharmaceutical sciences would be beneficialWhat will you be doing in this role? Extracting pharmacokinetic details of the therapeutic drug including the model (animal/human), dose, regime, and duration from scientific sourcesIndexing pharmacokinetic parameters measured (with substrate and technique) and the methods of evaluation from labels, references, posters, and conferencesCapturing drug-drug interactions and indexing overall effects and impacts that a drug-drug interaction could create on both pharmacokinetic and pharmacodynamic aspectsTo undertake any other reasonable duties as requested by your line manager / director on a permanent or temporary basis Product you will be developingCDDI focuses exclusively on pharma and drug development, harmonizing and integrating essential biological, chemical and pharmacological data from disparate sources into a single platform. Users will be benefited by using the broadest, deepest, most accurate source of R&D intelligence that has been manually curated, validated, and shared using a solution built by scientists for scientists. About the Team   DMPK team analyses scientific journals, patents, congress abstracts, and FDA documents and provides content to CDDI. External stakeholders would be scientists and pharma companies interested in identifying and validating drug PK and DDI behaviours. The DMPK knowledge area of CDDI provides continually updated information that supports drug research at every stage of drug development. Hours of Work  40 hours/per day 9:00 AM to 6:00 PM IST. This is a full-time positionAt 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.