Clinical Study Lead

ICON plc

Not specified; competitive within each country; ra...
Vendor oversight for clinical trials
Study protocol understanding and training
Cro etmf review and compliance
The role involves overseeing vendors to ensure adherence to budget, timelines, and organizational objectives for individual protocols

Job Summary

  • The role involves overseeing vendors to ensure adherence to budget, timelines, and organizational objectives for individual protocols.
  • Candidates will develop strong relationships with vendors and sites while ensuring continuity throughout all phases of the trial.
  • ICON offers a competitive salary, diverse benefits including health insurance and retirement planning, and a commitment to an inclusive culture.

Matching Summary

The role involves overseeing vendors to ensure adherence to budget, timelines, and organizational objectives for individual protocols.

Salary

Not specified; Competitive within each country; Range of additional benefits included

Skills & Requirements

Must-have

  • Vendor oversight for clinical trials
  • Study protocol understanding and training
  • CRO eTMF review and compliance
  • Budget and timeline management
  • Site readiness coordination

Nice-to-have

  • Strong vendor and site relationships
  • Continuous improvement recommendations
  • Mentorship of junior team members
  • Inclusive environment fostering innovation

Key Requirements

  • Undergraduate degree in clinical or science field
  • Minimum 5 years relevant experience
  • Minimum 3 years clinical research management role
  • Fluent English and host country language
  • Licensed healthcare professional preferred

Work Rights

Not specified

Tailored Resume

Cover Letter