cra - Budapest

ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. · Oversight of clini ...

+The Entry Clinical Research Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. · ...

We are seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. · We're proud to foster an inclusive environment driving innovation and excellence,We welcome you to join us on our mission to shape the future of clinical development. · ...

+ICON plc is a world-leading healthcare intelligence and clinical research organization. · +Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. · Conducting site visits to assess site perform ...

We are seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requireme ...

The Entry Clinical Research Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. · For those with medical and/or health/life science i ...

ICON plc is a world-leading healthcare intelligence and clinical research organization. We welcome you to join us on our mission to shape the future of clinical development. · We are currently seeking a Clinical Research Associate to join our diverse and dynamic team at ICON Plc. ...

Clinical Research Associate (CRA) role at ICON plc in Hungary. The position involves overseeing clinical trials, ensuring compliance, collecting data, and developing relationships with stakeholders. · Coordinate study activities. · Maintain study documentation. · Develop collabor ...

The Clinical Operations Lead is responsible for overseeing clinical operations of a project within a defined regional/global level.Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan ...

+ +The Clinical Operations Lead is responsible for the clinical operations of a project within a defined regional/global level. · + +Oversight of project deliverables and assigned Clinical Research Associate (CRAs) · Implementation of enrollment and recruitment strategies togethe ...

Manage clinical site monitoring services for one or more projects. · In-house based position responsible for project monitoring services including training site/patient recruitment data/document management budgets regulatory filings aligns SOPs study guidelines GCP best practices ...

The Entry Clinical Research Associate at Medpace offers an exciting career in drug and medical device development while making a difference in people’s lives.This could be the right opportunity for those with medical and/or health/life science interest and background who want to ...

We are seeking Experienced Ophthalmology CRA to complete our FSO team. · All aspects of study site monitoring including routine monitoring and close-out of clinical sites,maintenance of study files,conduct of pre-study and initiation visits;liaise with vendors;and other duties as ...

Manage clinical site monitoring services for projects including multiple services. In-house based position responsible for design and oversight of project monitoring services. · ...

+ Clinical Research Associate I + · We are currently seeking Experienced Ophthalmology CRA 1 to complete our FSO team. · You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in clinical trials.+ ...

The Clinical Scientist supports medical monitoring and scientific tasks on projects under theguidance of Therapeutic Medical Advisors (TMA) and in collaboration with the cross functional project team. These activities enable the use of high quality, scientific data to make timely ...

The Clinical Scientist supports medical monitoring and scientific tasks on projects under the guidance of Therapeutic Medical Advisors (TMA) and in collaboration with the cross functional project team. · Respond to protocol questions/CRAs/Sites under direction and supervision of ...

IQVIA is looking to hire a motivated Clinical Trial Assistant, Single Sponsor Dedicated, Hungary · Job Overview: · CTA performs daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accura ...

The Entry Clinical Research Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. · ...

We are looking for Clinical Research Associates to join our team. You will be responsible for ensuring that all site-level activities related to the study implementation are performed in accordance with the protocol, applicable regulatory requirements and Good Clinical Practice g ...