Labcorp Drug Development

As a leading contract research organization (CRO), Labcorp Drug Development provides comprehensive drug development solutions for a range of industries. Our services cover the preclinical, clinical and post-market phases of drug development, the product life cycles for medical device and diagnostics and development services paired with regulatory support for the chemical testing and crop protection industries.

Labcorp Drug Development is a global leader in nonclinical safety assessment, clinical trial testing and clinical trial management services. Our unique perspectives are based on decades of scientific, medical and regulatory expertise.

Did you know?

In July 2022, Labcorp announced its intention to spin off its clinical development business as a separate public company, subject to the satisfaction of certain customary conditions. Fortrea will become the new brand identity for our Clinical Development business in connection with the spin-off, which is expected in mid-2023.

We believe that the exceptional is possible when you have the right partner, so we are looking for the right people to help build a transformative force in Clinical Development. www.fortrea.com

Core responsibilities:

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  Documenting and tracking study activities using relevant forms and tools, as well as relevant Project Management System
  
  
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  Preparation of study site specific materials in accordance with relevant SOPs
  
  
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  Setting up and maintaining tracking systems for e.g. study supplies and investigator payments
  
  
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  Create and main contact list of study team members, study sites, and external suppliers/contract organizations
  
  
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  Support Investigator Meetings
  
  
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  Train and mentor less experienced Clinical Trial Administrators
  
  
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  Set up and maintain clinical investigator files and documentation
  
  
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  Assist with coordinating study level vendors as requested
  
  
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  Organize/prepare for client meetings/teleconferences
  
  
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  Liaise with all other departments to ensure the smooth running of the study as needed
  
  
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  Maintain paper trial master file documentation and tracking/archiving as applicable
  
  
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  Might be requested to work in a client facing environment
  
  
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  Perform other duties as assigned by management
  
  

Education and Qualifications:

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  Diploma - Secondary Education or equivalent
  
  
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  Previous administrative experience or equivalent training/experience in clinical trials is preferred
  
  
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  Good oral and written communication skills in Hungarian and English
  
  
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  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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