Offer summary
Qualifications:
Bachelor's Degree required; advanced preferred., 5+ years clinical research experience., 2-4+ years project management experience., Strong regulatory knowledge and GCPs., Proficient in MS Office Suite..Key responsabilities:
- Lead integration of project team activities.
- Manage CRO/vendor selection and operations.
- Provide strategic input on clinical trials.
- Generate country-specific Informed Consent Forms.
- Interface with multiple departments on projects.