Global Medical Advisor

**ABOUT THE JOB**

Want a 3D Career? Join Norgine.

At Norgine, our colleagues Dare themselves to be different and try new things, Drive to achieve their goals and beyond, and Develop themselves and their community.

We call it the 3D career at Norgine and it offers you a fully-rounded experience with no limits.

Bring everything about yourself that you’re proud of, whether that’s your passion for making a difference, focus on others’ well-being, or intellectual curiosity to unleash in a fast-paced environment and supportive community.

In return, get a sense of belonging, a long-term career with ongoing development and upskilling, and a company that cares about people’s wellness as much as you do.

Because at Norgine, we transform lives with innovative healthcare solutions.

We have an exciting opportunity for a Global Medical Advisor to join Norgine.

The person holding this position will report to Senior Global Director of Medical Affairs and be a member of the Global Development team.

The core responsibility of the role is to provide strategic global medical support and act as a global medical lead for designated products/brands, in order to support the development and commercialisation of the designated products/brands throughout their lifecycle

If you want a multi-dimensional 3D career in a leading healthcare organisation, join us.

**Requirements**:
**KEY RESPONSIBILITIES & ACCOUNTABILITIES**
- Providing medical support and contribution to overall strategic global brand plan development and lifecycle management as well as execution of the medical elements of the agreed brand/development plan to time and budget; the medical activities potentially being performed in a cross-functional fashion e.g. publication activities, advisory boards; External Experts engagement; congress & conference support; public relations activities; collaborative initiatives etc..
- Provide medical input to develop and review medical information, training as well as education and promotional materials.
- Deliver medical elements of training as required both internally and to appropriate external stakeholders
- Reviewer for global materials; carrying out copy approval for materials to comply with applicable Codes and Company standards and for the management of any code-related issues.
- Development and review of Medical Information, training and marketing materials.
- Planning, review and support for data generation activities including and not limited to Phase IV studies including health economic and real-world data programmes.
- Review and manage IST proposals, including liaison with business partners on study review.
- Liaison with PV Physicians to ensure safety reporting requirements from company-supported IST, NIS and market research studies are met.
- Support joint management committees with external partner companies
- Undertake and support due diligence activities for potential business opportunities.

**SKILLS & KNOWLEDGE**
- Medical or pharmacy qualification and UK Registration or equivalent further qualification in pharmaceutical medicine or allied disciplines preferred
- Broad-based experience in Medical Affairs and related roles, at Affiliate and Global levels.
- Brand management / medical brand support experience essential.
- Training and experience in copy approval and relevant codes of practice regulating the promotion of medicines and ideally medical devices
- Working knowledge of major aspects of operational drug and device safety
- Working knowledge of the drug development process
- Working knowledge of the medicines and devices regulatory processes in Europe
- Knowledge and skills should be maintained by appropriate updates and training.

This job description is a summary of the typical functions of the job - not an exhaustive or comprehensive list of all possible responsibilities, tasks and duties.

**Benefits**

Benefits vary between locations.