Pharmacovigilance Assistant
Há 6 dias
Job OverviewSupport pharmacovigilance team members with different activities and review, assess and process safety data and information, across service lines, received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations SOPs and internal guidelines under guidance and support of senior operation team members.**Essential Functions**- To Prioritize and complete the assigned trainings on time.- Process Safety data according to applicable regulations, guidelines, Standard Operating procedures (SOPs) and project requirements.- To perform Pharmacovigilance activities per project requirement including but not limited to, collecting and tracking incoming Adverse Events(AE)/endpoint information- determining initial/update status of incoming events- database entry- coding AE and Products, writing narratives, Literature related activities as per internal/ project timelines.- Ensure to meet quality standards per project requirements.- Ensure to meet productivity and delivery standards per project requirements.- To ensure compliance to all project related processes and activities.- Creating, maintaining and tracking cases as applicable to the project plan.- Identify quality problems, if any, and bring them to the attention of a senior team member.- To demonstrate problem solving capabilities.- To mentor new teams members, if assigned by the Manager.- Attend project team meetings and provide feedback to operations manager on any challenges/issues or successes.- 100% compliance towards all people practices and processes- Perform other duties as assigned.**Qualifications**- Bachelor’s Degree in scientific or healthcare discipline/life sciences graduation with 1-1.5 years of relevant experience.- Advanced level of English- Good knowledge of medical terminology.- Working knowledge of applicable Safety Database.- Knowledge of applicable global, regional, local clinical research regulatory requirements.- Excellent attention to detail and accuracy.- Strong organizational skills and time management skills.- Strong verbal/written communication skills.- Self-motivated and flexible.- Ability to follow instructions/guidelines, utilize initiative and work independently.- Ability to multi-task, manage competing priorities and deadlines.- Willingness and aptitude to learn new skills across Safety service lines.- Ability to establish and maintain effective communication and working relationships with coworkers, managers and clients.- Ability to work as a Team Player, contribute and work towards achieving Team goals.- Ensure quality of deliverables according to the agreed terms.- Demonstration of IQVIA core values while doing daily tasks
-
Pharmacovigilance Assistant Ii
1 semana atrás
São Paulo, Brasil ICON Plc Tempo inteiroPharmacovigilance Assistant IIICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical developmentWe are currently seeking a Pharmacovigilance Assistant II to join our...
-
Pharmacovigilance Assistant I
Há 2 dias
São Paulo, Brasil Icon Tempo inteiroPharmacovigilance Assistant I ICON plc is a world-leading healthcare intelligence and clinical research organization.We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.We are currently seeking a Pharmacovigilance Assistant I to join our...
-
Pharmacovigilance Assistant I
3 semanas atrás
São Paulo, Brasil ICON Tempo inteiroPharmacovigilance Assistant I ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Pharmacovigilance Assistant I to join our...
-
Pharmacovigilance Assistant I
Há 4 horas
São Paulo, São Paulo, Brasil ICON plc Tempo inteiroPharmacovigilance Assistant IICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical developmentWe are currently seeking a Pharmacovigilance Assistant I to join our...
-
Pharmacovigilance Assistant
Há 7 dias
São Paulo, Brasil IQVIA Tempo inteiroJob Overview Support pharmacovigilance team members with different activities and review, assess and process safety data and information, across service lines, received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations SOPs and internal guidelines under guidance and support...
-
Medical Contact Center Assistant I
Há 6 dias
São Paulo, Brasil Fortrea Tempo inteiroJoin to apply for the Medical Contact Center Assistant I role at Fortrea . Responsibilities Respond to medical information queries, product quality complaints, and general queries received via telephone, email, fax, etc. Receive information, record, and report adverse drug reactions within the required timelines according to regulations and internal WI/SOPs....
-
Contract Marketing Assistant
2 semanas atrás
Sao Paulo, Brasil Ultragenyx Pharmaceutical Inc. Tempo inteiro**Why Join Us?**- Be a hero for our rare disease patients_- _Our commitment and care for patients extends to our people, so culture is an essential cornerstone for Ultragenyx. We remain continuously focused on creating a supportive and inclusive environment of profound learning and growth - so employees can thrive in all areas of their lives, in and outside...
-
Medical Contact Center Assistant I
Há 6 horas
São Paulo, São Paulo, Brasil Fortrea Tempo inteiroSummary Of ResponsibilitiesTo respond to medical information queries/product quality complaints/general queries that may be received over the telephone call, email, fax etc.Receive information, record, and report Adverse Drug Reaction in timelines (according to the regulations and to internal WI/SOPs) that may be received over telephone calls, email, fax...
-
Clinical Research Associate Ii
Há 8 horas
Sao Paulo, Brasil MSD Tempo inteiro**Responsibilities include, but are not limited to**: - The role is accountable for performance and compliance for assigned protocols and sites in a country; - Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our company policies and procedures, quality standards and adverse event...