Not specified; competitive within each country; in...
2 years experience in icf writing
Proficient knowledge of ich/gcp guidelines
Experience with ethics committee queries
This role is crucial for ensuring the accuracy, compliance, and timely approval of informed consent forms for global clinical trials
Job Summary
This role is crucial for ensuring the accuracy, compliance, and timely approval of informed consent forms for global clinical trials.
The successful candidate will serve as a key point of contact for sponsors and functional leads to optimize project outcomes.
ICON offers a competitive salary along with comprehensive benefits including health insurance, retirement planning, and flexible country-specific perks.
Matching Summary
This role is crucial for ensuring the accuracy, compliance, and timely approval of informed consent forms for global clinical trials.
Salary
Not specified; Competitive within each country; Includes various annual leave entitlements and health insurance offerings
Skills & Requirements
Must-have
2 years experience in ICF writing
Proficient knowledge of ICH/GCP guidelines
Experience with Ethics Committee queries
Nice-to-have
Protocol interpreting and review skills
Strong analytical and problem-solving abilities
Mentorship and coaching capabilities
Key Requirements
4 to 8 years experience in Feasibility, Start Up and Site Activation
Minimum 2 years experience in Informed Consent Form writing/development