About The Position

As a Clinical Research Associate at PSI you will be involved in improving patients' lives while enjoying a variety of monitoring tasks and working on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry. Home-based in Portugal

Requirements

  • College/University degree in Life Sciences or an equivalent combination of education, training & experience.
  • At least 2 years of independent on-site monitoring experience in Portugal.
  • Full working proficiency in Portuguese, English and MS Office applications.
  • Ability to plan, multitask and work in a dynamic team environment.
  • Communication, collaboration, and problem-solving skills.
  • Ability to travel and valid driver’s license.

Nice To Haves

  • Experience in Oncology, Hematology is a plus.

Responsibilities

  • Conduct and report all types of onsite monitoring visits
  • Be involved in study startup
  • Perform CRF review, source document verification and query resolution
  • Be responsible for site communication and management
  • Be a point of contact for in-house support services and vendors
  • Communicate with internal project teams regarding study progress
  • Be involved in site identification process
  • Support regulatory team in preparing documents for study submissions
  • Prepare for and participate in audits and inspections

Benefits

  • extensive training programs
  • profound therapeutic area trainings
  • monitors training program
  • mentorship programs
  • interactive soft-skills trainings
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