Project Manager Clinical Operations
Zizers, CH
In this role, you will be required to:
Main Responsibilities:
• Plan and manage clinical studies within the framework of scientific and legal guidelines
• Prepare, coordinate, oversee and if required, conduct site initiation visits, monitoring visits and site close-out visits including report review
• Coordinate the development of adapt Clinical Investigation Plans, Case Report Forms, Final Study Reports and provide operational expertise as required.
• Coordinate and develop essential documents for the execution of clinical studies
• Coordination of internal study team and external CRAs and subcontractors (CROs) involved on project level
• Validation of clinical data
• Control quality of clinical data
• Compile and archive study documents
• Main contact person for budget development and budget tracking
• Periodic review of study budgets including timelines planned.
• Provide status information on study data to AO ITC management and sponsor as required
• Maintain contact with study sites personnel (Principal Investigators and Study Nurses)
• Evaluate clinical data in collaboration with the Biostatistician, the Medical Advisor and the Medical Writer
• Assist in development of scientific publication
In order to master this challenge, you have:
Required Education:
• MSc in natural science
Required Experience:
• Basic medical knowledge
• Experience with project management
• Interest in methodological questions
• Strong organizational and follow-up skills
• Attention to detail and reliability
• Ability to work both independently and in a team
• Flexibility and customer-focused mindset
• Strong written and oral communication skills in German and English
We offer
- An interesting and varied job in an exciting and innovative organization
- The opportunity to be part of a highly committed international team
- Modern infrastructure
- Employment conditions which match the requirements and offer a high degree of flexibility regarding working hours and location