Clinical Research Lead Assistant

ICON

Frankfurt, Germany
Clinical trial documentation management
Regulatory document preparation
Clinical trial coordination
ICON plc is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence.
  • The role involves providing administrative support for clinical trials, ensuring compliance with study protocols and regulatory requirements, and collaborating with cross-functional teams to support trial operations.
  • ICON offers competitive salary and a range of benefits focused on well-being and work-life balance, including health insurance, retirement planning, and global employee assistance programs.

Matching Summary

ICON plc is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence.

Skills & Requirements

Must-have

  • clinical trial documentation management
  • regulatory document preparation
  • clinical trial coordination
  • trial progress monitoring
  • site communication management

Nice-to-have

  • strong organizational skills
  • problem-solving skills
  • collaborative teamwork
  • attention to detail
  • multitasking abilities

Key Requirements

  • advanced degree or certification in life sciences or clinical research
  • extensive clinical trial support experience
  • solid understanding of clinical trial processes
  • knowledge of regulatory requirements

Work Rights

Not specified

Tailored Resume

Cover Letter