IQVIA Safety Operations
team plays an important part in the design, build and execution of end-to-end safety solutions for major pharmaceutical companies and their post market products around the world. We are proud to be an international, diverse team based across the world, with ‘safety hubs’ in Ireland, Poland, Austria, Portugal, Slovakia, Spain, India and USA. Each new joiner is supported by a nurturing management team, collaborative colleagues as well as a clear career ladder with plenty of opportunities to allow you to grow, adapt and shine. Medical Information and Adverse Event Intake Specialist with Danish and English language This position will put you at the forefront of Patient Safety. With daily direct contact with Health Care Professionals (HCPs) and patients (the very people we are working to help), this is a highly visible and important role within IQVIA and essential to our core goal of patient safety. You will perform key medical information call centre services and process safety and product quality information to help optimize the safety profiles of products across various therapeutic areas. This role can be conducted either Home Based / Hybrid / Office based - the choice is yours. RESPONSIBILITIES Provide phone support to health care professionals and consumers regarding adverse events, product quality complaints, medical inquiries, product support, and other needs as required. This does NOT include commercial sales support. Process Lifecycle safety operational data, perform data entry for tracking and Lifecycle safety databases, coding medical terminology, generating queries pertinent to the case, performing quality control, driving case closure, coordinating translations. Receive and document incoming telephone calls and emails from investigative sites or other sources reporting safety data. Build a positive, collaborative team environment with Lifecycle safety team members, lead by example, provide training and mentoring for less experienced team members. Provide regular feedback to operations team manager and Customer Delivery manager (CDM) on project metrics and challenges. Liaise with Project Manager by proactively identifying issues and proposing solutions, providing them with technical support, reports, metrics, identifying SOW changes and potential change orders, delegating client requests. Participate in training across Lifecycle safety process service offerings, participate in working groups as applicable in implementation of new initiatives, identification and implementation of process efficiencies. MINIMUM REQUIRED EDUCATION AND EXPERIENCE Bachelor’s Degree in a Life Science is required. Excellent written and verbal skills in English (min. C1) and Danish language (min. C2 / native). Knowledge of
Norwegian language
will be considered a valuable plus. Experience in Lifecycle safety (Pharmacovigilance, CEVA, Medical Information, Safety Publishing, Risk Management etc.) is an asset. Excellent attention to detail and accuracy maintaining consistently high-quality standards. Ability to work effectively on multiple projects simultaneously, organize own workload and effectively manage competing priorities. Excellent organizational skills and time management skills. This role is not available for UK visa sponsorship. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
https://jobs.iqvia.com
#J-18808-Ljbffr
team plays an important part in the design, build and execution of end-to-end safety solutions for major pharmaceutical companies and their post market products around the world. We are proud to be an international, diverse team based across the world, with ‘safety hubs’ in Ireland, Poland, Austria, Portugal, Slovakia, Spain, India and USA. Each new joiner is supported by a nurturing management team, collaborative colleagues as well as a clear career ladder with plenty of opportunities to allow you to grow, adapt and shine. Medical Information and Adverse Event Intake Specialist with Danish and English language This position will put you at the forefront of Patient Safety. With daily direct contact with Health Care Professionals (HCPs) and patients (the very people we are working to help), this is a highly visible and important role within IQVIA and essential to our core goal of patient safety. You will perform key medical information call centre services and process safety and product quality information to help optimize the safety profiles of products across various therapeutic areas. This role can be conducted either Home Based / Hybrid / Office based - the choice is yours. RESPONSIBILITIES Provide phone support to health care professionals and consumers regarding adverse events, product quality complaints, medical inquiries, product support, and other needs as required. This does NOT include commercial sales support. Process Lifecycle safety operational data, perform data entry for tracking and Lifecycle safety databases, coding medical terminology, generating queries pertinent to the case, performing quality control, driving case closure, coordinating translations. Receive and document incoming telephone calls and emails from investigative sites or other sources reporting safety data. Build a positive, collaborative team environment with Lifecycle safety team members, lead by example, provide training and mentoring for less experienced team members. Provide regular feedback to operations team manager and Customer Delivery manager (CDM) on project metrics and challenges. Liaise with Project Manager by proactively identifying issues and proposing solutions, providing them with technical support, reports, metrics, identifying SOW changes and potential change orders, delegating client requests. Participate in training across Lifecycle safety process service offerings, participate in working groups as applicable in implementation of new initiatives, identification and implementation of process efficiencies. MINIMUM REQUIRED EDUCATION AND EXPERIENCE Bachelor’s Degree in a Life Science is required. Excellent written and verbal skills in English (min. C1) and Danish language (min. C2 / native). Knowledge of
Norwegian language
will be considered a valuable plus. Experience in Lifecycle safety (Pharmacovigilance, CEVA, Medical Information, Safety Publishing, Risk Management etc.) is an asset. Excellent attention to detail and accuracy maintaining consistently high-quality standards. Ability to work effectively on multiple projects simultaneously, organize own workload and effectively manage competing priorities. Excellent organizational skills and time management skills. This role is not available for UK visa sponsorship. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
https://jobs.iqvia.com
#J-18808-Ljbffr
