מדעים/ביוטק
QUALIFICATIONS:
• Experience in CR&D roles/responsibilities or equivalent
• Proficient knowledge of GCP/ICH, drug development process from discovery
to registration,
study design, statistics, clinical operations
• Excellent verbal, written, communication and interpersonal skills.
• Experience in CR&D roles/responsibilities or equivalent
• Proficient knowledge of GCP/ICH, drug development process from discovery
to registration,
study design, statistics, clinical operations
• Excellent verbal, written, communication and interpersonal skills.
לפרטים נוספים
מדעים/ביוטק
Responsibilities:
Design and develop all clinical study documents, Submits all relevant study
documents to EC/IRB, CA and/or FDA, local authorities and institutions.
Design and develop all clinical study documents, Submits all relevant study
documents to EC/IRB, CA and/or FDA, local authorities and institutions.
לפרטים נוספים