QPL IQVIA RDS Poland

Our team is growing join us on our mission to drive healthcare forward!ResponsibilitiesPerform site monitoring visits (selection initiation monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements i.e. Good Clinical Practice (GCP) and In More...

Job OverviewUnder general supervision perform tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations standard operating procedures (SOPs) project requirements and contractual/budgetary guidelines. May al More...

Job Overview*For this role you must have at least 5 years of oncology experience as a CPMProject Leads are an integral part of clinical trial delivery liaising with clinical teams to improve patients lives by bringing new drugs to the market faster. The Project Lead is an essential me 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...

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...

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...

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...

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...

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...

General Description: The Senior Clinical Investigator Payment Associate for Poland will undertake activities to provide specialized support and assistance to the Clinical Business Operations department and all studies in the Site Payment portfolio. This role partners closely with inve More...

As a Senior Safety Aggregate Reporting Specialist you will apply knowledge and expertise for Safety Aggregate Report and Analytics (SARA) Center deliverables including signal management activities safety aggregate reports literature surveillance and benefit risk management documents.M More...

Summary:The Global Business Operations (GBO) team is a dynamic group with high visibility within IQVIA. GBO develops strategic proposals and budgets for our customers and upon award drives contract execution including changes throughout the study lifecycle by working with numerous int More...

assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the agreed timelines. Performs Senior Review of straightforward medical writing deliverables. Negotiates timelines and discusses/resolves customer comments.Provides More...

We are seeking an Associate Director Laboratory Operations Antibody Discovery Services to join IQVIA Laboratories in Durham NC.We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purp More...

IQVIA Biotech is hiring Clinical Research Associates!Join IQVIA today and make an impact on patients outcome!Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol applicable More...