CTC / Clinical Trial Coordinator - sponsor dedicated, Warsaw
1 miesiąc temu
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
We are looking to hire a Clinical Trial Coordinator in Warsaw, Poland.
In this position, you will be fully dedicated to a single sponsor and you will have a full-time and permanent contract .
Core responsibilities:
Documenting and tracking study activities using relevant forms and tools, as well as relevant Project Management System Preparation of study site specific materials in accordance with relevant SOPs Setting up and maintaining tracking systems for e.g. study supplies and investigator payments Create and main contact list of study team members, study sites, and external suppliers/contract organizations Support Investigator Meetings Train and mentor less experienced Clinical Trial Administrators Set up and maintain clinical investigator files and documentation Assist with coordinating study level vendors as requested Organize/prepare for client meetings/teleconferences Liaise with all other departments to ensure the smooth running of the study as needed Maintain paper trial master file documentation and tracking/archiving as applicable Might be requested to work in a client facing environment Perform other duties as assigned by managementEducation and Qualifications:
Diploma - Secondary Education or equivalent Previous administrative experience or equivalent training/experience in clinical trials is preferred Good oral and written communication skills in Polish and English Organized and has the ability to multi-taskFortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact.
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