Medical Director for Vaccine Development
vor 1 Monat
Valneva is a specialty vaccine company that develops, manufactures, and commercializes prophylactic vaccines for infectious diseases addressing unmet medical needs. Our team is committed to making a positive impact on global public health. We are a global company with operations in multiple countries, and we are open to people of all backgrounds. Our diverse and inclusive workforce makes Valneva a great place to work.
**Job Summary**
We are seeking a Medical Director for Vaccine Development to provide specialist support to global vaccine development related medical activities. This role will involve developing the Medical Monitoring and Oversight concept on program level and implementing it on trial level. The successful candidate will also manage external teams of regional medical monitors, support Clinical Strategy, and provide relevant medical input to essential documents.
**Responsibilities**
* Develop and implement Medical Monitoring and Oversight concepts on program level and trial level
* Manage external teams of regional medical monitors
* Support Clinical Strategy in the development and maintenance of professional and credible relationships with key opinion leaders
* Provide relevant medical input to essential documents
* Provide training to internal and external stakeholders on medical contents
* Keep abreast of professional information through conferences and medical literature
* Act as a therapeutic area subject matter expert
* Ensure compliance with applicable processes concerning Medical Monitoring and interface with Clinical Safety
* Ensure budgets, timelines, and compliance requirements are factored into programs' medical activities
**Requirements**
* Medical Doctorate (degree and experience in Clinical Development are mandatory
* Relevant therapeutic experience in immunology or vaccinology preferred
* At least 3 years of experience in clinical development
* Experience of managing cross-functional global teams on development program level
* Ability to run Medical Monitoring/Medical Oversight of assigned programs/trials
* Knowledge of clinical trial methodology, regulatory requirements, and experience in review and interpretation of clinical trial protocols
* Sound understanding of clinical safety requirements
* Excellent oral and written communication skills
**What We Offer**
* Open, appreciative company culture with innovative spirit and attractive assignments
* International surrounding with flat hierarchies
* Good team spirit in a strong and highly motivated team
* Wide range of benefits like flexitime, compensation days, performance-related bonus, lunch vouchers, child care center, company events, myClubs, full access to LinkedIn Learning, ...
**Note**
Due to legal reasons, we are obliged to disclose the minimum salary for this position, which is € gross per year based on full-time employment. However, our salaries are market-oriented and in line with your qualifications and experience.
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