Clinical Research Associate 2/ Sr CRA1 - based in Slovakia

• Your responsibilities will include:

  • Performing site selection, initiation, monitoring and close-out visits
  • Supporting the development of a subject recruitment plan
  • Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines
  • Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions
  • Collaborating with experts at study sites and with client representatives

  
  Qualifications:

  • University degree in scientific discipline or health care
  • Requires at least 2 year of on-site monitoring experience.
  • Very good computer skills including MS Office
  • Excellent command of Ukranian and English language.
  • Organizational, time management and problem-solving skills
  • Ability to establish and maintain effective working relationships with coworkers, managers, and clients
  • Flexibility to travel
  • Driver’s license class B

  What you can expect:

  • Resources that promote your career growth
  • Leaders that support flexible work schedules
  • Programs to help you build your therapeutic knowledge
  • Excellent working environment in a stabile, international, reputable company
  • Company car or car allowance, mobile phone and attractive benefits package
• External Job Description

  External Job Description
  Clinical Research Associate

  Your responsibilities will include:

  • Performing site selection, initiation, monitoring and close-out visits
  • Supporting the development of a subject recruitment plan
  • Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines
  • Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions
  • Collaborating with experts at study sites and with client representatives

  
  Qualifications:

  • University degree in scientific discipline or health care
  • Requires 2 plus year of on-site monitoring experience.
  • Very good computer skills including MS Office
  • Excellent command of Slovak and English language.
  • Organizational, time management and problem-solving skills
  • Ability to establish and maintain effective working relationships with coworkers, managers, and clients
  • Flexibility to travel
  • Driver’s license class B

  What you can expect:

  • Resources that promote your career growth
  • Leaders that support flexible work schedules
  • Programs to help you build your therapeutic knowledge
  • Excellent working environment in a stabile, international, reputable company

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.