Onsite Clinical Research Associate 2 – CFSP

Posted 5 days ago

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About the role

  • Junior Clinical Research Associate at IQVIA supporting site management in clinical trials across Spain. Key responsibilities include site selection, monitoring visits, and regulatory compliance.

Responsibilities

  • 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

Requirements

  • University degree in scientific discipline or health care
  • Experience in Pharma Industry, and/or Clinical Trials environment
  • Very good computer skills including MS Office
  • Excellent command of Spanish 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

Benefits

  • 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
  • Mobile phone and attractive benefits package

Job title

Clinical Research Associate 2 – CFSP

Job type

Experience level

JuniorMid level

Salary

Not specified

Degree requirement

Bachelor's Degree

Location requirements

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