Clinical Research Physician
il y a 4 semaines
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.
You will be the first member of the cross-functional team that will be put in place to support the (pre-)launch of a new molecule in Alzheimer’s disease.
We are ideally looking for a physician with medical affairs experience with strong strategic, cross-functional teamwork and leadership skills. You will be in charge of the development and the execution of the medical plan in line with product/disease state strategy, project/budget management, thought leader engagement, identifying data gaps for getting product access and training of sales force. On top of the medical projects, the Clinical Research Physician/Clinical Research Scientist has a broad responsibility, requiring teamwork with the reimbursement department, the RWE manager, the marketing and clinical operations department.
You are a member of the Medical Affairs Team and are reporting to the Medical Director in Belgium.
**RESPONSIBILITIES**
**Business/customer support (pre and post launch support)**
- In depth product knowledge and knowledge of the therapeutic area (Alzheimer’s disease) and the treatment options
- Contribute to the development of medical strategies to support brand commercialization activities by working closely with the global Medical Affairs and brand teams, Global Patient Outcomes/Real World Evidence and global Price, Reimbursement and Access (PRA), clinical management or personnel and other cross-functional management during the development of the local business plan.
- Contribute as a scientific and medical expert to activities and deliverables of the PRA organization, in particular giving clinical input and insight to defend the product value.
- 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 archetypes and potential influence on the medical interventions for the product.
- Take a leadership role in defining the Patient Journey and corresponding Moments of Truth based on his/her medical knowledge. Become patient advocate, as well as a medical expert.
**Scientific Data Dissemination/Exchange**
- Knowledge of and compliance with local laws and regulations with respect to data dissemination and interactions with external health care professionals.
- Understand and actively address the unsolicited scientific information needs of external health care professionals according (if they cannot be answered by medical information service)
- Organize advisory board meetings and/or other meetings with health care professionals.
- Support medical information associates in preparation and review of medical letters and other medical information materials.
- Support development of slide sets and publications (abstracts, posters, manuscripts).
- Establish and maintain appropriate collaborations and relationships with external scientific experts, 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**
- Understand and keep updated with the pre-clinical and clinical data relevant to the molecule.
- Identify data gaps and generate RWE to support local access.
- Participate in investigator identification and selection, in conjunction with clinical teams.
- Review IIT proposals and publications, and guide in submission of the proposal.
**Regulatory Support Activities**
- Participate in review of local labeling collaboration with Regulatory Affairs.
- Demonstrate deep knowledge of local label.
**Scientific/Technical Expertise and continued development**
- Be aware of current trends and projections for clinical practice and access in the therapeutic area(s) relevant to the product, both near term (1-2 years) and longer-term (3-5 years).
- Critically read and evaluate the relevant medical literature; know the status and data from competitive products; and keep updated with medical and other scientific developments relevant to the product.
- Responsible for the scientific training of the clinical study team.
- Act as scientific consultant for clinical study team members, others in medical and cross-functionall
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