Location: Vienna, Austria (Maximum 5 days in the office / month)
About the Company
We are partnered with an innovative company specialising in the development, manufacturing, and commercialisation of vaccines. They have successfully advanced several vaccines from early research to regulatory approval, and have a current portfolio of three proprietary travel vaccines.
About the Role
In this role, you will be responsible for leading and managing all aspects of one or more clinical trials (Phase I-IV), from protocol development to final trial report submission.
Main Responsibilities
- End-to-end trial oversight of one or more global Vaccine trials
- Ensure compliance with ICH-GCP, FDA/EMA regulations, and other relevant guidelines and SOPs.
- Oversee operational trial deliverables, ensuring they are met within established timelines, budget constraints, and quality standards.
- Manage relationships with CROs and other external partners, ensuring adherence to project scope, timelines, and budget.
- Collaborate effectively with various internal departments and functional areas.
- Travel may be required to oversee and coordinate clinical studies.
Main Requirements
- Advanced degree in Life Sciences or a related field
- Minimum of 3 years of experience in end-to-end Clinical Project Management
- In-depth knowledge of ICH-GCP, data protection laws, clinical trial directives, and other relevant regulations.
- Experience in CROs and/or CRAs oversight
- Excellent communication, presentation, and interpersonal skills, with strong problem-solving abilities and financial management experience.
- Fluent in English (both spoken and written)
How to Apply
If you are interested, apply here for a confidential discussion about this role.