QPL IQVIA RDS Poland

The IQVIA Internship provides you with the opportunity to gain relevant project-based work experience at one of the most successful and cutting-edge global clinical research units in the market while building relationships within the company that will impact your future.You will be wo More...

IQVIA is seeking a Sr. CRA 1 or CRA 2 with a minimum of 1.5 years of on-site oncology monitoring experience:Essential FunctionsPerform site monitoring visits (selection initiation monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements More...

At IQVIA we are continuously expanding the boundaries of whats possible in clinical development through advanced analytics cutting-edge technology and deep scientific expertise. Within our Research & Development Solutions (RDS) organization we are enhancing our services with agent More...

Join Our Team as a Therapeutic Strategy Lead!Are you passionate about creating innovative delivery strategies that meet customer needs Do you thrive in a collaborative environment where you can make a real impact If so we have the perfect opportunity for you!PurposeAs a Therapeutic St More...

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 More...

Join IQVIA as a CRA / SrCRA (m/w/d) in our Clinical Site Management department home-based throughout Germany. You will focus on a comprehensive clinical trial management in a variety of indications and learn about the diverse scientific approach of the sponsors. Beside establishing st More...

The IQVIA Internship provides you with the opportunity to gain relevant project-based work experience at one of the most successful and cutting-edge global clinical research units in the market while building relationships within the company that will impact your future.You will be wo More...

IQVIA is looking to appoint statistical programmers to utilize the SAS programming language to develop clinical study report materials according to the objectives of a clinical trial for regulatory submissions. Programming and performing related tasks serving the full spectrum of stat More...

Job OverviewCreate Linguistic Validation and eCOA quotations performing necessary research on existing translations.Essential FunctionsEstablish new processes and improve upon existing processes related to project support.Manage the set up and maintenance of all project quotation file More...

Job OverviewLocation: home-based in Poland Senior Global Trial Managers (SGTMs) are an integral part of clinical trial delivery leading and working alongside clinical teams to improve patients lives by bringing new drugs to the market faster. The SGTM is a member of the core project t More...

*This is a Remote opportunity based in EMEAThe IQVIA Obesity Center of Excellence a hub of Obesity clinical innovation is looking for exceptional Board-Certified physicians to join our team as a Medical Strategy Lead to help us expand our Obesity and Metabolic portfolio and advance th More...

Job OverviewManage the execution of the assigned clinical study (ies) from initiation through to closeout. Ensure that clinical study management and project deliverables are on time and is in accordance with standard operating procedures (SOPs) policies and practices. To provide proje More...

Associate Project Manager eCOALocation: Spain Italy Greece Poland Portugal Bulgaria home-basedJob OverviewMaintains and validates the project scope plans and schedules for moderately complex projects; adheres to established metrics for project success; applies standards (e.g. delivery More...

Principal Statistical Programmer Standards Location: home-based anywhere in the United States or Canada Position Summary:IQVIA is hiring to expand a sponsor-dedicated team working fully within the environment of a prominent Pharma company supporting their long-term standards initiativ More...