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:
The purpose of the Senior Associate Consultant / Consultant - VEO role is to work with cross-functional, multidisciplinary teams to develop strategic summaries on the value of our medicines for our key priority products and indications.
The Senior Associate Consultant / Consultant - VEO role combines scientific knowledge and communication skills in order to organize and deliver relevant RWE information that are meaningful and relevant for Lilly and for our customers.
The Senior Associate Consultant / Consultant - VEO role is a recognized technical expert for RWE deliverables.
Primary Responsibilities:
Align with cross-functional teams on value evidence needs. Therapeutic area understanding (15%)
- Work with teams to ensure a deep understanding and clear documentation of the key priority needs that our customers have for RWE evidence, for our key priority products and indications and how this evidence supports they key product messages.
- Develop a plan to provide timely updates to the teams on the value of our medicines in clinical practice for the selected needs and priority products and indications.
- Maintain and enhance clinical and therapeutic knowledge, including disease state, product, and competitor data
RWE project delivery. Analyze and synthesize published evidence (80%)
- Perform regular/periodic literature searches and critical appraisal of RWE studies to identify strengths and weaknesses of different study approaches and designs.
- Provide balanced, scientifically based, consistent and accurate RWE summaries for internal and external use.
- Summarize search findings with key messages and synthesize published evidence in different formats, depending on our customers’ needs (narrative summaries, visual presentations, etc.)
- Store final deliverables in an appropriate storage system. Update the information and communicate the findings on a regular basis.
Customer Focus (5%)
- Network with others to identify process or strategic improvements, share best practices and suggest opportunities where appropriate.
- Identify trends, make recommendations, and drives initiatives to improve customer experience.
- Demonstrate flexibility and availability in the event of scheduling adjustment or unexpected events.
- Engage in activities supporting reward and recognition, teambuilding, and diversity.
Minimum Qualification Requirements
- Bachelor’s Degree with at least 5-7 years’ experience and/or knowledge in health outcomes research/real world evidence/healthcare consulting/competitive intelligence.
- Knowledge, experience and understanding of healthcare data used in outcomes research.
- Experience in medical, scientific or technical writing fields (at least 3-5 years)
- Cognitive abilities including verbal reasoning, attention to detail, critical thinking, and analytical ability.
- Strong comprehension and communication skills including the ability to translate and disseminate complex scientific information in a clear and concise manner
- Excellent written and verbal communication skills and high attention to detail
- Demonstrated ability to influence and collaborate within and across teams
- Demonstrated project management and time management skills.
- Strong interpersonal skills and the ability to be flexible in varying environments and with multiple customer groups.
- Demonstrated high-level end-user computer skills (e.g., word processing, tables and graphics, spreadsheets, presentation, and templates)
Other Information/Additional Preferences:
Other Information:
- Project Management experience would be an advantage
- Epidemiology, clinical pharmacology, therapeutic area, or other medical and scientific specific knowledge and experience (e.g., immunology, diabetes, or oncology expertise).
- Expertise with understanding the pros and cons of different approaches to generate Real World Evidence.
- Publication experience.
- Ability to work well independently and as part of a team.
Additional Preferences:
- Ability to work well across cultures and time zones.
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
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