Offer summary
Qualifications:
Master's degree in science or related discipline, Minimum of 5 years of CDM experience, Experience with global regulatory submissions, Knowledge of data management processes and technologies, Familiarity with regulatory guidelines and best practices.
Key responsabilities:
- Liaise between company and CRO for Data Management
- Provide oversight for CRO Data Management team
- Collaborate on study design and various processes
- Review clinical study protocols and provide comments
- Manage relationships with external vendors