Offer summary
Qualifications:
Bachelor's degree in life sciences or a related field, Minimum 6 years of relevant work experience, Minimum 6 years of experience in drug development and/or clinical research, Strong knowledge of regulatory requirements and GCP, Excellent project management, leadership, and communication skills.
Key responsabilities:
- Developing and implementing strategic plans for clinical trials in different therapeutic areas
- Overseeing trial management, budget allocation, team leadership, regulatory compliance, risk management, vendor and data management
- Ensuring safety monitoring, effective communication, quality assurance, and documentation of all trial-related activities