Cra Ii - Romania

ICON Clinical Research, LP

Bucharest, Romania
Not specified; competitive salary mentioned; vario...
Fully remote
2 years of cra monitoring experience
Oncology clinical trial experience
Valid driving license required
ICON Clinical Research is seeking a Clinical Research Associate II (CRA II) to join their team in Bucharest, Romania, focusing on monitoring clinical studies in phases II-IV. The role requires strong monitoring experience, particularly in oncology, and involves substantial travel. ICON promotes an inclusive culture and offers a range of attractive benefits

Job Summary

  • ICON is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation.
  • The role involves working independently to coordinate activities for setting up, monitoring, and closing out investigational sites for phases II–IV studies.
  • ICON offers competitive benefits including health insurance, retirement planning, and a global Employee Assistance Programme focused on well-being.

Matching Summary

Match Score: 85

ICON Clinical Research is seeking a Clinical Research Associate II (CRA II) to join their team in Bucharest, Romania, focusing on monitoring clinical studies in phases II-IV. The role requires strong monitoring experience, particularly in oncology, and involves substantial travel. ICON promotes an inclusive culture and offers a range of attractive benefits.

Salary

Not specified; Competitive salary mentioned; Various annual leave entitlements; Health insurance offerings; Retirement planning offerings; Global Employee Assistance Programme

Skills & Requirements

Must-have

  • 2 years of CRA monitoring experience
  • Oncology clinical trial experience
  • Valid driving license required
  • 60% travel requirement domestic and international
  • Knowledge of ICH-GCP guidelines

Nice-to-have

  • Experience mentoring less expert CRAs
  • Ability to work in fast-paced environment
  • Excellent written and verbal English communication
  • Experience with feasibility studies
  • International project leadership experience

Key Requirements

  • 2 years monitoring experience in phase I-III trials
  • Oncology experience required
  • Located in Bucharest without travel restrictions
  • Valid driving license mandatory

Work Rights

Not specified

Tailored Resume

Cover Letter