Offer summary
Qualifications:
Minimum of 3 years' experience in clinical trials., Proven ability to lead cross-functional teams., Experience monitoring oncology clinical trials., Familiarity with ICH-GCP guidelines..
Key responsabilities:
- Deliver clinical study components at the country level.
- Prepare country financial agreements and maintain budgets.
- Lead Local Study Team for compliance and performance.
- Ensure timely preparation and submission of consent forms.
- Liaise with regulatory authorities for study submissions.