Join us on our exciting journey!IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients.
Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.
Joining IQVIA, the world’s leading comprehensive Human Data Sciences organization and working in partnership with a major Pharma company, these positions 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, essential to our core goal of patient safety.
Infectious diseases, Immunology and Inflammation; HIV & Oncology.
You will benefit from joining the largest safety department in the world and working within an industry-leading, best-practice environment.
To ensure you contribute to the business and grow your career, you will also benefit from ongoing training and development from our in-
house safety experts to plan and progress your MI / PV career
In these combined MI / PV roles, you will use both your scientific background and your language expertise to share medical information and receive and document adverse events.
You will be required to perform key medical information call center services and review, assess and process safety and product quality information to help optimize the safety profiles of products marketed around the world.
You may be in regular communications with our client, patients and HCPs and for some roles, depending on levels of experience, you will be required to lead and provide oversight and could be a subject matter expert / trainer in each therapeutic area.
This does NOT include commercial sales support except managing medical information requests forwarded by the sales representative on behalf of an HCP.
related tasks as needed e.g. regulatory reporting