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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.
**Job summary**
**Main Accountability/responsibility**
**Scientific expertise and Medical Affairs Delivery**:
- Develop and/or contribute to the affiliate/therapeutic area (TA) medical plan and strategies along with CRP.
- Lead / support data analysis and the development of slides and publications (abstracts, posters, manuscripts).
- Partner with other existing Medical Affairs roles Clinical Research Physicians (CRP), Clinical Research Scientists (CRS), and Medical Science Liaison (MSL) to achieve a seamless medical team aimed at delivering exceptional customer experiences through medical education initiatives, using where possible various omnichannel engagement tools.
- Contribute to insight collection in the respective disease area pertaining to patient journey, treatment patterns, unmet needs, etc. Along with the field medical teams (MSLs).
- Support CRP in preparing and executing data generation plans in line with the affiliate’s business requirements.
- Medical information letter creation (local) and review (regional/global) in collaboration with Med Info function.
- Support the initiation, oversight, and follow-up of Medical Affairs studies (clinical trials, real world evidence, etc.).
- Support the execution and management of externally sponsored/initiated research/trials.
- Support Scientific Data Disclosure (SDD plans).
- Serve / Support as the affiliate medical/scientific leaders including research and regulatory deliverables, where required in collaboration with the CRP.
- Critically read and evaluate relevant medical literature to be current in the TA.
- Keep up to date with Medical and other Scientific developments relevant to the product/portfolio.
- Be aware and identify current trends, issues and projections for clinical practice and access.
**Cross functional Team collaboration**:
Serve as the key medical point of contact for the cross functional teams including the commercial team:
- Contribute clinical, scientific and strategic input to support the cross functional team.
- Serve as a key resource for Medical Launch support.
- Contribute to the development of medical strategies for brand plans.
- Offering scientific and creative input, contribute to the development (local materials) and/or review global/regional materials of promotional materials for the brand team.
- Effectively communicate and transfer knowledge of the therapeutic available solutions environment, the clinical landscape and relevant medical and scientific knowledge.
- Oversee the medical component of the local Patient Support Programs Serve as a key resource to support the medical training needs of internal Business Partners such as Sales and Marketing.
- Oversee the collation and analysis of customer information to drive understanding and insights and pro-actively anticipate issues/challenges and raise them to relevant stakeholders.
- Deliver scientific, educational, and promotional presentations internally and to customers.
- Lead/support the planning and implementation of symposia, advisory boards, scientific exchange, speaker trainings and educational meetings/events with HCPs as needed.
- Provide recommendations for thought leaders (TLs) and other external parties to serve as consultants or faculty.
- Identify, support, and train Lilly contracted speakers.
- Effectively lead collaborate with alliance partners.
- Partner with CRP/CRS and act as back up when needed.
**Customer Engagement & Experience**:
- Respond to external customer questions and needs, including escalations by Med Info & Sales in accordance with the company-wide requirements for responding to unsolicited requests for information.
- Drive the local coordination of activities and engagement of Thought Leaders.
- Develop and maintain collaborations and relationships with relevant professional societies.
- Deliver scientific, educational and occasionally meetings organized by commercial teams (whether virtual or face to face).
- Collaborate cross-functionally to drive improvements in customer engagements through digital innovations.
- Take a leadership role in medical to deliver positive customer experiences.
**Collaboration with Regulatory**:
- Participate in development and review of local labeling and labeling modifications in collaboration with affiliate CRP, global development, brand teams, regulatory, and legal. Demonstrate deep knowledge of local label.
- Provide medical expertise to regulatory