Clinical Trial Data - Software Development

☞ gloor & lang Pharma and Biotech Recruiting

View: 204

Update day: 21-03-2024

Location: Oberwil (BL) Basel-Landschaft BL

Category: IT - Software

Industry: Staffing Recruiting

Position: Entry level

Job type: Full-time

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Job content

Cloud based Software for next level Pharma Research

You look for crativity and intellectual space to bring your own ideas to the table ? You are excited to design, build and deliver a solution utilizing the latest technology for a highly regulated healthcare industry ?

Get started in new Software Development for Clinical Data Crunching. Your solutions will help pharma industry to get quick grasp of trends in Clinical Studies. Join an innovative young health care provider that starts to offer cloud based Software Solutions for Clinical and Medical use. The young start-up is designing and developing an application utilizing Blockchain technology for the pharmaceutical industry.

Your role:
  • The software product development lifecycle for a specific product group including development, backlog maintenance, planning & review, test & release management
  • Responsible for the communication and management of the external development team within your product group
  • Facilitating customized solution developments for customers, and clients to help improve and increase business
  • act as internal know-how base for Data Management
Your profile :
  • +5 years of IT work experience preferably in clinical research
  • Experience with clinical trials data management or healthcare data management
  • A solid technical background in software development processes
  • Knowledge of SCRUM, preferably Product Manager and/or Owner experience
  • Understanding and preferably experience with Quality Management systems and procedures (Guidelines, Standards, SOPs etc.)
If you possess knowledge in topics like 21CFR11, ICH-GCP and other relevant pharma regulations this would be a very strong asset for the new team. Some knowledge in decentralized clinical trials will be helpful as well as experience with systems such as EDC, eTMF, CTMS, Pharmacovigilance, etc.

You are a strong communicator with interpersonal, strategic, analytical, and organizational skills. Let’s talk together!

__Interested? We are looking forward to get in touch with you.

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Deadline: 05-05-2024

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