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Clinical Research Associate II

2 mesi fa

Milano, Lombardia, Italia PSI A tempo pieno

Job Overview

As a Clinical Research Associate at PSI, you will be responsible for conducting and reporting onsite monitoring visits, participating in study startup, and performing CRF review and query resolution. You will also be involved in site communication and management, and will be a point of contact for in-house support services and vendors.

Key Responsibilities

  • Conduct and report onsite monitoring visits
  • Participate in study startup
  • Perform CRF review and query resolution
  • Manage site communication and relationships
  • Coordinate with internal project teams
  • Participate in feasibility research
  • Support regulatory team in preparing documents
  • Prepare for and participate in audits and inspections

Requirements

  • University/College degree in Life Sciences or equivalent
  • At least 2 years of independent onsite monitoring experience in Italy
  • Experience in all types of monitoring visits in Phase II and/or III
  • Experience in Oncology/Gastroenterology therapeutic areas is a strong advantage
  • Full working proficiency in English and Italian
  • Proficiency in MS Office applications
  • Ability to plan, multitask, and work in a dynamic team environment
  • Communication, collaboration, and problem-solving skills
  • Ability to travel

About PSI

  • PSI is a stable, privately-owned company with a strong reputation in the industry
  • We offer extensive onboarding and mentorship programs, profound therapeutic area trainings, and interactive soft-skills trainings
  • Our team collaboration is high on our agenda, and we aim for employees to feel valued and heard in friendly and supportive teams
  • PSI CRAs have the opportunity to work with different Sponsors on a variety of therapeutic areas