Manager, Drug Safety Content Analysis

Job SummaryWe are looking for Manager Drug Safety Content Analysis to join our Pharmacovigilance (PV) team (offices working in Hybrid model). This is an amazing opportunity to support the team to perform literature monitoring and assessing for adverse events reporting, indexing, and abstracting by using broad knowledge of scientific terms and medical terminology, drugs, therapeutic areas, and pharmacovigilance regulations.The Manager Drug Safety Content Analysis will manage and supervise project’s PV Operations/training staff on a day-to-day basis, guiding performance of PV Operations staff in ongoing projects in terms of training, quality of deliverables, compliance with the timelines and relevant trainings.About You – experience, education, skills, and accomplishmentsMaster’s Degree in life Sciences, Health or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics etc.).A degree in Dentistry/physiotherapy/Nursing, which involves patient exposure in hospital-based environment, would be an advantageAround 10 years of experience reviewing biomedical literature for adverse event reporting and atleast 5 years of team management experienceExcellent leadership and line management skillsExcellent knowledge of drug safety and the drug development processClient focused approach to workAbility to manage multiple and varied tasks and prioritize workload with attention to detailAbility to train and mentor peopleIt would be great if you also had the following:Certification from a professional medical writer’s associationExperience with commercial and client-specific biomedical literature databasesScientific/medical writing backgroundWhat will you be doing in this role?Providing functional expertise/oversight of process and handling queries of the PV Operations staffCreateParticipation in meetings with client and within team, as needed.Performing activities delegated to the PV Operations staff in case of unplanned peaks or urgent requirementsPrepare for and respond to internal/external audits/inspectionsTaking suitable action as per client feedback for any performance or process related concernsProviding project updates to the Senior Management on periodic basisAssisting his/her manager for operational day-to-day activitiesAbout the TeamThe PV Literature team supports multiple customers covering all therapeutic areas. It is a supportive working environment with personalized training, and opportunities to engage in different aspects of pharmacovigilance and participate in customer upgrade planning if desired.Hours of WorkThis is a full-time permanent position working weekdays (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.