Senior Global Clinical Trial Associate - Warsaw

The Associate Clinical Trial Liaison (CTL) will develop relationships with clinical trial investigators and research site staff to facilitate recruitment of subjects in pharmaceutical industry clinical trials for which ICON serves as the CRO. · Understand the scientific basis of ...

We are seeking a Trial Master File Associate to join our CDS Ophthalmology Trial Master File team. As part of this role, you will work alongside passionate and innovative professionals to ensure our customers achieve their goals. · ...

We are seeking a Trial Master File Associate to join our CDS Ophthalmology Trial Master File team as part of our Clinical Development Services (CDS) division.The successful candidate will be responsible for organizing and maintaining the Trial Master File (TMF) according to compa ...

The Associate Director will lead end-to-end analytics delivery for clinical trials managing a global project team. · ...

We are looking for a Trial Master File Associate to join our CDS Ophthalmology Trial Master File team. As part of our team you will work alongside passionate and innovative professionals to ensure our customers achieve their goals. · ...

We are seeking an experienced and dynamic Associate Director, Clinical Trial Lead to join our Global Development Operations team. This role is pivotal in leading high-impact, global Phase III and registrational clinical trials. You will be responsible for driving operational exce ...

BMS is seeking an experienced Associate Director Line Manager for Global Clinical Trial Management to join our dynamic Global Development Operation's Team in Warsaw Poland. · Manage performance and career development of Global Trial Leads GTLs and other trial management staff as ...

We are seeking a Senior Clinical Associate to join our diverse and dynamic team. · We will provide administrative and project tracking support to the Project Manager(s) and Clinical Trial Manager(s), emphasizing inspection readiness. · Support operational aspects of managed trial ...

Coordinador responsable por desarrollar estrategias operativas e informativas para envíos clinicos necesarios a nivel europeo. · Lidera discusiones, · consolida input · ,facilita discusiones via planificación escenarios. · ...

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.Our success depends on the quality of our people. That's why we've made it a priority to build a diverse cult ...

We are currently seeking a Senior Clinical Associate to join our diverse and dynamic team. · Adhere to applicable SOPs WIs policies codes of Good Clinical Practice GCP local regulatory requirements etc.Comply with relevant training requirementsAssist in trial specific document ma ...

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Challenging meaningful life-changing those aren't words that are usually associated with a job but working at Bristol Myers Squibb is anything but usual here uniquely interesting work happens every day in every department from optimizing a production line to the latest breakthrou ...

Job summary: · Senior Site Manager is a mid-level site management role with typically 3-5 years of experience. · ...

This is an ideal opportunity for professionals with backgrounds in consulting clinical operations or trial analytics who are ready to take ownership of delivery and help shape the success of global studies. · ...

We are currently seeking a Senior Clinical Research Associate 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 requi ...

We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, · Bachelor's degree in a scientific or healthcare-related field. · ...

We are seeking a Site Management Associate II to join our team. As a Site Management Associate II at ICON, you will play a vital role in supporting the management and monitoring of clinical trial sites by ensuring compliance with study protocols, regulatory requirements, · Variet ...

We are currently seeking a Site Management Associate II to join our diverse and dynamic team. · ...

We are seeking a Site Management Associate II to support the management and monitoring of clinical trial sites by ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice guidelines. · Coordinating monitoring activities at clinical trial sites ...