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Pozíció leírása / Job description

Organisation/Department

 

Join our brand new team in Hungary and be a part of this outstanding opportunity. Clairo has a US headquarters with 30 facilities in nine countries. If you would like to work in a full remote setup and you would like to make an impact in the clinical trial industry, then this one of a kind company is for you!

 

Clario. The Best of ERT & Bioclinica! Two industry leading companies merged together to generate the richest clinical evidence.  

 

Clario delivers the leading endpoint technology solutions for clinical trials. Through experience gained from over 19,000 clinical trials delivered in support of 870 regulatory approvals, Clario fuses scientific expertise and global scale into the broadest endpoint technology platform to enable pharmaceutical, biotech and medical device partners to transform lives. Through Trial Anywhere™, Clario has mastered the ability to generate rich evidence across all trial models: decentralized, hybrid and site-based clinical trials. With 30 facilities in nine countries across North America, Europe and Asia Pacific, Clario’s global team of science, technology and operational experts has been delivering the richest clinical evidence for nearly 50 years.

 

What we offer: 

  • A real diverse Multicultural environment
  • We support your professional development through internal and external training and certification programs
  • Global employee exchange program, meaning you can apply to work in any of our global locations for 4 weeks

Our System Analyst (SAS Programmer) will

  • Perform any and all functions as required to meet corporate commitments and deliverables
  • Receive and review non-Clario standard client file specifications from Project Manageror client and interact with the client to finalize transfer specifications
  • Develop SAS programs to create non-standard data files, specifically vertical file and incremental data file requirements
  • As part of the Software Development Life Cycle, review User Requirements and create and/or review Functional and Technical Specifications and approve specifications
  • Create and test ad-hoc programs for Esoteric quality control checks requested by QC
  • Data resolution/mining
  • Other client requirements
  • Assist with orientation and training of Systems Analysts and Data Management / Project Management personnel as determined by management.
  • In conjunction with the entire department, recommend, develop and implement SOPs for improved CDP Procedures.

Elvárások / Requirements

What we seek -

  • BS in computer sciences or related field; MS in computer sciences related field helpful.
  • Minimum three years experience in BASE SAS products and procedures and one year experience in database design and data structures.
  • Understanding of the pharmaceutical drug development process, ideally gained through a minimum of two years experience in the pharmaceutical or healthcare industry. 
  • Strong organization, analytical and communication skills.
  • Detail-oriented.
  • Experience with Windows and Microsoft Office products.
  • Experience with DB programming is a plus.
  • Local to Hungary
  • Ability to work from home on a regular

Amit nyújtunk / Benefits

Join our Budapest team as a System Analyst to provide world class customer service over the phone in support of clinical trials deployed at hundreds of clinical sites worldwide.

Are you an experienced SAS Programmer, ideally with Clinical experience? Joining our Budapest team as a Systems Analyst will put you at the heart of our operations. Liaising with our Data Management teams and external clients, you will ensure the high quality research and analysis performed by Clario experts is translated into accurate and relevant data files for our clients

Randstad Hungária Kft. logó

System Analyst

Budapest
Full time

Published on 13.07.2022

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