Offer summary
Qualifications:
Degree in medical or related science, Minimum two years in clinical research, Experience in Hungarian regulatory processes, Knowledge of ICH GCP and regulations, Multilingualism preferred.
Key responsabilities:
- Act as a subject matter expert for regulatory submissions
- Plan and track documents for submissions and activations
- Communicate status, risks and actions on start-up activities
- Provide country/site/EC requirements for site activation
- Initiate and develop relationships with investigators