Informed Consent Specialist

ICON

Bangalore, India
Not specified; not specified; competitive within e...
4 to 8 years feasibility start up site activation experience
Minimum 2 years icf writing development experience
Proficient knowledge of ich/gcp guidelines
The role is crucial in ensuring the accuracy, compliance, and timely approval of informed consent forms for global clinical trials

Job Summary

  • The role is crucial in ensuring the accuracy, compliance, and timely approval of informed consent forms for global clinical trials.
  • Candidates will serve as a key point of contact for sponsors and functional leads to optimize project outcomes and resolve ethics committee queries.
  • ICON offers a competitive salary along with comprehensive benefits including health insurance, retirement planning, and flexible country-specific perks.

Matching Summary

The role is crucial in ensuring the accuracy, compliance, and timely approval of informed consent forms for global clinical trials.

Salary

Not specified; Not specified; Competitive within each country with various annual leave entitlements and health insurance offerings

Skills & Requirements

Must-have

  • 4 to 8 years Feasibility Start Up Site Activation experience
  • Minimum 2 years ICF writing development experience
  • Proficient knowledge of ICH/GCP guidelines
  • Strong English writing and communication skills

Nice-to-have

  • Protocol interpreting and review capability
  • Ability to mentor new hires during onboarding
  • Experience representing department at audits

Key Requirements

  • 4-8 years experience in Feasibility, Start Up, and Site Activation
  • Minimum 2 years experience in ICF writing/development
  • Proficient knowledge of applicable country regulations

Work Rights

Not specified

Tailored Resume

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