Medical Affairs Professional

Il y a 7 mois

Brussels, Belgique Lilly Temps plein

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.

**Purpose**:
We are looking for an experienced Medical Affairs Professional who is complementary to the current team with strong strategic, cross-functional teamwork and leadership skills. Responsibility for specific activities will be agreed within the team and include collaboration to the development and execution of the medical plan in line with product/disease state strategy, project/budget management, thought leader engagement, identifying data gaps for getting or maintaining product access, training of sales force. On top of the medical projects, Medical Affairs Professionals have a broad responsibility, requiring teamwork with the reimbursement department, the RWE manager, the marketing and clinical operations departments.

In this role, you will be a member of our Diabetes/Obesity Medical Affairs Team and you will report to the Belgian Medical Director. You will work in close collaboration with a dedicated Medical Advisor obesity and a dedicated MAP diabetes.

**Responsibilities**:
Responsibilities will be discussed and agreed within the team aligned with specific strengths of team members and workload.

Your primary responsibility will be diabetes and developing a strong collaboration between the diabetes and obesity cross-functional team aligning strategic and medical content. You will be responsible for specific projects from start to end, but always making sure the team is aware of objectives and progress. You engage with Thought Leaders by involving them in medical projects or get insights on new data. You will be responsible for local scientific data dissemination (presenting at locally Lilly organized meetings, independent national/regional conferences and hospital staff meetings).

You also provide expert medical support to all aspects of the local business, to ultimately enhance the customers' experience in interacting with the company, contribute to the development and review of promotional material, training of the sales force.

**Business/customer support (pre and post launch support)**
- In depth product knowledge and knowledge of therapeutic area (diabetes) and the treatment armamentarium
- Understand and anticipate the scientific information needs of all local/regional customers
- Contribute to the development of medical strategies to support brand commercialization activities by working closely with the global Medical Affairs and brand teams, Global and local Real World Evidence, corporate affairs and clinical trial management personnel
- Contribute as a medical expert to activities and deliverables of the PRA organization and defend the product value
- Contribute actively on an ongoing basis to the strategic planning for currently marketed brands
- By offering scientific and creative input, contribute to the development, review, and approval of promotional materials for the brand team
- Support training of sales representatives, and other medical representatives
- Become familiar with market evolution and potential influence on the medical interventions for the product

**Scientific Data Dissemination/Exchange**
- Knowledge of and compliance with local laws and global policies with respect to data dissemination and interactions with external health care professionals
- Address the unsolicited scientific information needs of HCPs (if they cannot be answered by medinfo service)
- Data sharing and contribution to educational meetings by providing topics/content, do the speaker briefings or being a speaker
- Organize advisory board meetings
- Development of slide sets and publications (abstracts, posters, manuscripts)
- Establish and maintain appropriate collaborations and relationships with scientific experts and thought leaders
- Develop and maintain appropriate collaborations and relationships with relevant professional societies
- Provide congress support (for example, availability to answer questions at exhibits, provide oral and poster presentations, staff medical booth, meet thought leaders, and participate in customer events)

**Clinical Research**
- Review strategic alignment of local Investigator Initiated Trial (IIT) proposals and guide in submission of the proposal
- Identify data gaps and generate RWE for getting or maintaining local access

**Regulatory Support Activities**
- Review of local labeling in collaboration with regulatory affairs
- Demonstrate deep knowledge of local label

**Scientific/Technical Expertise and continued

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