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ICON Clinical Research, LP

Germany
Not specified; competitive salary offered; range o...
Not specified
Conducting site qualification initiation monitoring visits
Ensuring protocol compliance and patient safety
Performing data review and query resolution
ICON Clinical Research is seeking a Clinical Research Associate II in Germany, responsible for conducting various phases of clinical trials, ensuring compliance, and collaborating with site staff. The ideal candidate should have a relevant bachelor's degree, at least two years of experience in clinical research, and strong organizational skills

Job Summary

  • ICON is a world-leading healthcare intelligence and clinical research organization dedicated to shaping the future of clinical development.
  • The role involves conducting site qualification, initiation, monitoring, and close-out visits while ensuring protocol compliance and data integrity.
  • Benefits include competitive salary, various annual leave entitlements, health insurance, retirement planning, and a global Employee Assistance Programme.

Matching Summary

Match Score: 85

ICON Clinical Research is seeking a Clinical Research Associate II in Germany, responsible for conducting various phases of clinical trials, ensuring compliance, and collaborating with site staff. The ideal candidate should have a relevant bachelor's degree, at least two years of experience in clinical research, and strong organizational skills.

Salary

Not specified; Competitive salary offered; Range of additional benefits provided

Skills & Requirements

Must-have

  • Conducting site qualification initiation monitoring visits
  • Ensuring protocol compliance and patient safety
  • Performing data review and query resolution
  • Valid driver's license required
  • Ability to travel at least 60% of time

Nice-to-have

  • Strong organizational and communication skills
  • Attention to detail in fast-paced environment
  • Collaborative team player with independent work ability

Key Requirements

  • Bachelor's degree in scientific or healthcare-related field
  • Minimum of 2 years experience as Clinical Research Associate
  • In-depth knowledge of ICH-GCP guidelines and regulations
  • Valid driver's license required
  • Willingness to travel at least 60% domestically and internationally

Work Rights

Not specified

Tailored Resume

Cover Letter