Added
10 days ago
Type
Full time
Salary
Salary not provided

Related skills

mentoring client management clinical trials regulatory submissions ich-gcp

๐Ÿ“‹ Description

  • Monitor and own the progress of clinical studies at investigative sites and ensure that clinical
  • Coordinate all necessary activities required to set up and monitor a study (i.e., identify
  • Handle appropriately sized clinical trials and support clinical study teams with trials that are
  • Train and mentor junior staff members.
  • Interact directly with clients, initiate payments, and participate in proposal activities

๐ŸŽฏ Requirements

  • 4-year college degree or equivalent experience
  • Holder of CRA certificate
  • Minimum 5 years of CRA/SCRA experience within a CRO, pharmaceutical, biotechnology, or medical
  • Experience monitoring clinical trials across a variety of therapeutic areas
  • Availability for domestic travel including overnight stays, which may constitute up to
  • Fluency in English and the local language is required

๐ŸŽ Benefits

  • Empowered to make an impact and build meaningful client relationships
  • Opportunity to grow career in an environment that values quality, accountability, and professional
  • Fully home-based within Hungary
  • Opportunity to train and mentor junior staff members
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