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ICON Clinical Research, LP

Philippines
Not specified; competitive within country; various...
University degree in medicine or science
Knowledge of ich-gcp guidelines
Ability to travel approximately 60%
The role involves delivering high-standard clinical trial monitoring work while coordinating study setup and maintenance activities independently

Job Summary

  • The role involves delivering high-standard clinical trial monitoring work while coordinating study setup and maintenance activities independently.
  • Candidates must ensure patient safety by strictly adhering to ICON's procedures, protocols, and regulatory requirements.
  • ICON offers a competitive salary along with diverse benefits including health insurance, retirement planning, and global employee assistance programs.

Matching Summary

The role involves delivering high-standard clinical trial monitoring work while coordinating study setup and maintenance activities independently.

Salary

Not specified; Competitive within country; Various annual leave entitlements; Health insurance offerings; Retirement planning offerings

Skills & Requirements

Must-have

  • University degree in medicine or science
  • Knowledge of ICH-GCP guidelines
  • Ability to travel approximately 60%
  • Excellent written and verbal English communication

Nice-to-have

  • Strong social skills for timely query resolution
  • Experience reviewing medical data
  • Collaborative relationship building with site staff

Key Requirements

  • University degree in medicine, science, or equivalent
  • Knowledge of ICH-GCP guidelines
  • Willingness to travel approximately 60%

Work Rights

Not specified

Tailored Resume

Cover Letter