Beschreibung
Global Medical Director Established Products / Scientific Director (m/f/d)
Reference: -en
Start: asap
Duration: 12 MM++
Main tasks:
- Responsible for or contributes to (depending of the product portfolio) developing and implementation of medical strategy and tactics and ensuring alignment with the overall brand strategy in collaboration with International Portfolio Leader
- The company's medical an scientific expert for the assigned product(s), who provides expert input for the internal and external stakeholders (e.g. to address Regulatory Authority requests)
- Stay abreast of internal and external developments and trends to maintain a fully up-to- date view of internal/external context for the assigned product(s) to ensure optimal medical affairs response in addressing patient needs
- Ensure effective and efficient use of resources and acts in line with legal, regulatory and company's standards and codes of practice
Main qualifications
- University Degree in Life Sciences (required), an advanced Clinical/ Science Degree (preferred) (e.g., MD, PharmD, PhD, etc.) with profound experience in pharmaceutical industry, in medical function at global or country level preferably in the areas of oncology, immunology
- Experience and strong knowledge of the overall drug development process
- Experience with development of insights driven medical strategy and tactics, before and after product launch, including medical communications, patient/HCP engagement as well as design and conduct of clinical trials; authoring experimental protocols and/or study results and conclusions
- Proven expertise in dealing with wide range of data/ information and developing/ responding to various requests: clinical safety/ regulatory/legal, etc
- Considerable experience in external collaboration & stakeholder management: TAEs as well as consultants, contractors and agencies
- Excellent collaboration, communication and presentation skills, fluency in English is required, additional languages are advantageous
- High self-motivation, ability to work autonomously and as part of a cross-functional team
- Track record of making decisions and aligning the organization behind them
- Experience of writing clinical publications, expert reports and other regulatory documents such as PBRER and DSUR, etc
Main advantages:
- You will work in an international environment
- A very renowned company
About us:
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.
My contact at Hays:
Referencenumber:
Make contact:
Phone:
Email: