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.

Did you know?

Labcorp's Clinical Development and Commercialization Services business is now Fortrea in connection with its planned spin-off from Labcorp, which is expected in mid-2023. Fortrea’s spin-off from Labcorp is subject to satisfaction of certain customary conditions. This spin-off will position both organizations for accelerated growth and allow each to focus resources on distinct strategic priorities, customer and employee needs and value creation opportunities. As a provider of phase I-IV clinical trial management, regulatory guidance, patient access solutions and market access consulting, Fortrea will partner with both emerging and large pharmaceutical, biotechnology, device and diagnostic companies to drive healthcare innovation and improve the lives of patients worldwide.

Fortrea is looking for problem-solvers and creative thinkers who are passionate about breaking down barriers faced by sponsors of clinical trials, and who are committed to helping transform the development process to get promising life-changing ideas and therapies to patients faster. Join us as we cultivate a workspace where all employees have the opportunity to grow and make impacts on a global scale. For more information and questions related to Fortrea, please visit www.fortrea.com .

Fortrea is looking to hire a Financial Clinical Trial Administrator in Poland.

In this position, you will be fully dedicated to a single sponsor and you will have a full-time and permanent contract.

As a Fortrea employee dedicated to an FSP project, you will bring your specialized discipline to a core team working directly with one sponsor. Whether your specialization is in clinical monitoring, clinical project management, data management, biometrics or pharmacovigilance, we have an FSP opportunity to match your area of expertise.

With the support of exceptional people and an energized purpose, you’ll be empowered to own your career journey with dedicated mentoring, training and personalized development planning.

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 management

Requirements:

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-task

Labcorp is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.

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