Patient & Site Engagement Opeations Specialist - Sponsor Dedicated (m/w/d) - Budapest

Our ever-growing Lifecycle Safety Medical team is expanding. We are hiring Associate Medical Safety Directors in Portugal, Hungary, Slovakia, Romania, Bulgaria, Serbia, Ukraine and Croatia. The role participates in all aspects of the Medical Safety activities as per scope of work ...

We are looking for a Global Studies Asset Manager to lead · and drive operational study management delivery · of one or more molecule assets. This role involves · working closely with internal teams, partner operations, · cross-functional experts, vendor partners.Leverage PDG' ...

This Patient & Site Engagement Operations Manager will collaborate with pre-award stakeholders to manage patient recruitment operational plans on small/mid-size studies. · ...

Patient Recruitment and Retention operational plans on small/mid size studies. Collaborate with sponsors and project teams to implement and monitor impact of the recruitment/retention tactical plan. Represent IQVIA Patient Recruitment at site/sponsor-facing meetings to present st ...

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. Position may be responsible for the implementation of smaller programs in their enti ...

We are seeking a new colleague to join our dedicated team at the National Institute of Oncology as a Clinical Research Coordinator. · Performing administrative and organizational tasks related to clinical trials · Collaborating with the investigational team, IKEB, and pharmaceuti ...

We are seeking a new colleague to join our dedicated team at the National Institute of Oncology as a Clinical Research Coordinator. · Performing administrative and organizational tasks related to clinical trials · Collaborating with the investigational team, IKEB, and pharmaceuti ...

We are seeking a new colleague to join our dedicated team at the National Institute of Oncology as a Clinical Research Coordinator. · Performing administrative and organizational tasks related to clinical trials · Collaborating with the investigational team, IKEB, and pharmaceuti ...

The Senior Clinical Data Manager role is a great opportunity to work within our sponsor dedicated department and have this unique relationship with a sponsor. · ...

This role will be dedicated to one of IQVIA's largest clients through a Functional Service Provider (FSP) type partnership. This means you get all the benefits of working for an industry leading global CRO while operating within a sponsor environment and utilizing sponsor systems ...

A Clinical Research Coordinator position at the National Institute of Oncology. We are seeking a new colleague to join our dedicated team. · Performing administrative and organizational tasks related to clinical trialsCollaborating with the investigational team, IKEB, and pharmac ...

We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. · We are agile and driven to accelerate the delivery of therapies, · Serves as subject matter expert within the organiza ...

As Site Activation Lead, you ensure clinical trials move from plan to reality without unnecessary delays, protecting timelines, budgets, and most importantly — patient access to new therapies. · Variuos annual leave entitlements/li>A range of health insurance offeringsCompetitive ...

+We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. · +Acts as Functional Lead for Data Management including primary contact for internal liaison between Data Management/O ...

IQVIA Biotech is seeking a Senior Site Feasibility Specialist to support our growing clinical operations team. In this role, you will lead country-level site activation activities and ensure timely start-up of investigative sites in alignment with global and local regulations. · ...

As an experienced individual contributor within IQVIA Biotech's Regulatory Affairs team you'll operate under limited supervision to drive regulatory strategy and delivery across complex multi-stakeholder projects. · You'll lead cross-functional regulatory workstreams prepare and ...

We are responsible and accountable for the customer-focused leadership and management of Site Start-Up (SSU) deliverables within a country, region or globally, within the assigned projects or programs. · Directs the technical and operational aspects of the Site Start-Up deliverab ...

The Strategy Lead is an experienced project leader and principal author within Syneos Health's Global Risk Management & REMS (GRMR) business. · You will define the strategy and authoring approach for EU Risk Management Plans (RMPs) and additional Risk Minimisation Measures (aRMMs ...

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

Clinical research associate responsible for overseeing clinical trials from a centralized location. Conducts remote monitoring to ensure compliance with regulations and protocols. · ...