Global Trial Manager, Late Phase Studies, Single-Sponsor Dedicated - Warszawa, mazowieckie

IQVIA is hiring Clinical Research Associates · Join IQVIA today and make an impact on patients' outcome · Job Overview · Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, appl ...

IQVIA is hiring Clinical Research Associates · Join IQVIA today and make an impact on patients' outcome · Job Overview · Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, appl ...

Join IQVIA today and make an impact on patients' outcome as a Clinical Research Associate in Poland. · ...

Senior Global Trial Manager – Single Sponsor · Are you experienced in managing late phase clinical trials at a global level? · We are looking for a Senior Global Trial Manager to join our Single Sponsor Department. · Join our global team and take ownership of delivering late-ph ...

The IQVIA Sponsor-Dedicated Clinical Trials Assistant Team is supporting the project teams in the execution of clinical trials. Joining the team provides the opportunity to work with the preparation and documentation of clinical research projects in different therapeutic areas. Y ...

The IQVIA Sponsor-Dedicated Clinical Trials Assistant Team is supporting the project teams in the execution of clinical trials. Joining the team provides the opportunity to work with the preparation and documentation of clinical research projects in different therapeutic areas. Y ...

We are hiring a Study Start-Up Lead to join a sponsor-dedicated team and drive the successful planning and activation of clinical trials. · Partner closely with Clinical Operations to improve study start-up metrics and implement optimized processes. · Provide leadership, oversigh ...

Collaborate with leading pharma companies to help patients worldwide as a sponsor-dedicated Senior CRA in Poland. Enjoy stability, resources, and direct experience with clients. · ...

We are looking for a Global Studies Asset Manager to lead and drive the operational study management delivery of one (or more) of our molecule assets. · This position holds responsibility for clinical operations management and execution. · Product Development´s mission is to impr ...

We are looking for a Global Studies Asset Manager to lead and drive the operational study management delivery of one (or more) of our molecule assets. This position holds responsibility for clinical operations management and execution. · Have a minimum 3 years of relevant operati ...

Collaborate with pre and post award stakeholders to manage the coordination planning quality and implementation of Patient Recruitment and Retention operational plans on small/mid size studies. · ...

Warsaw, Poland | Full time | Home-based | R1530731 · Global Clinical Project Manager - Vendor Management Expert – Single Sponsor · Are you an experienced Vendor Management professional looking to make an impact in global clinical trials? · We are seeking a Global Clinical Project ...

Global Clinical Project Manager - Vendor Management Expert – Single Sponsor · Are you an experienced Vendor Management professional looking to make an impact in global clinical trials? · We are seeking a Global Clinical Project Manager - Vendor Management Expert to join our Singl ...

We are seeking a Global Clinical Project Manager - Vendor Management Expert to join our Single Sponsor Department. · ...

This is a strategic oversight role within a Centre of Excellence environment, focused on Risk-Based Monitoring (RBM) implementation and monitoring team oversight. · The position requires mandatory on-site presence in Warsaw three days per week, with limited travel.Develop and exe ...

We're looking for a Compliance QA Tester (CQA) to join our QA team. · Hunting for bugs and weird behaviors every single day · Writing clear, to‑the‑point bug reports in English · ...

IQVIA Biotech is seeking a Senior Site Feasibility Specialist to support our growing clinical operations team. · ...

Reference 25000PR1 · Responsibilities · Overview · : · If you are looking for a challenging and rewarding opportunity to continue your career, we encourage you to apply for this exciting role. · Your future scope of responsibility will cover: · Performing KYC/AML and other regula ...

We are seeking a Head of Affiliate Regulatory & Pharmacovigilance to lead all regulatory affairs and pharmacovigilance activities for our CEERTMEA operations. · ...

Company Description · At Nielsen, we are passionate about our work to power a better media future for all people by providing powerful insights that drive client decisions and deliver extraordinary results. Our talented, global workforce is dedicated to capturing audience engagem ...