Real World Evidence - Senior/Associate Mgr

Key Skills

Data Analysis, Data Analytics, Design, R Programming, SAS

Job Description

Eli Lilly and Company discovers, develops, manufactures, and sells pharmaceutical products worldwide. The company offers products across a broad range of therapeutic areas including: Diabetes, Oncology, Psoriasis, Psoriatic arthritis, Rheumatoid arthritis, Lupus and Gastrointestinal disorders. Eli Lilly and Company was founded in 1876 and is headquartered in Indianapolis, Indiana.

Our purpose: Lilly unites caring with discovery to create medicines that make life better for people around the world.

Responsibilities:

Primary Responsibilities: This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. Consult with your supervisor regarding your actual job responsibilities and any related duties that may be required for the position.

Development of Dashboards

• Design, develop and deliver user friendly and interactive dashboards per business requirements
• Work closely with internal business partners to develop solutions which meet the business needs
• Develop detailed documentation & specifications with cohort and variable definitions
• Provide direction to internal partners on best possible dashboard structures
• Present dashboard and data insights to the internal partners
• Maintain and revise dashboards as and when needed
• Seek out opportunities to attract and develop new dashboards with the help of new internal partners and customers within Lilly
• Demonstrate skills by helping team refine and standardize processes and dashboard related documents

RWE Project Delivery

• Work in routine with GPORWE scientists to conduct RWE methods research and develop timelines and working plan
• Perform in-depth research on disease background and understand the business need thoroughly
• Independently develop and finalise study documents such as high-level research protocols, statistical analysis plans and analysis specifications
• Conduct data analysis with variety of data sources ensuring quality and efficiency, while maintaining documentation and complying with pre-defined study standards
• Influence or negotiate change of timelines and content with scientists
• Develop project report and deliver tables, figures, listings according to specifications
• Assist publication process and collaborate with medical writing team to ensure timely delivery of abstracts, posters and manuscripts
• Contribute to RWE process improvements, including projects that make RWE COE staff more efficient.
• Provide database and other tool (e.g., RWE analytic tools) expertise.
• Lead, scope, and deliver data broker projects to give a GPORWE scientist list of potential data sources for their research.

Customer Focus & Pilot work

• Work with internal and external experts to develop and prepare
• Network with others to identify and share best practices globally
• Pilot new work and evaluate/make recommendation on the new work
• Train yourself as and when required to support diversification of work
• Engage in activities supporting reward and recognition, team building, and diversity
• Support cross-functional coaching, mentoring, and training

Basic Requirements:

• Bachelor’s/Master’s Degree with at least 2-5 years’ experience and/or knowledge in health outcomes research, statistical analysis, and epidemiology
• Knowledge, experience and understanding of healthcare data sources used in outcomes research
• Demonstrated mastery of written English with experience in medical, scientific or technical writing fields (at least 1 year); professional verbal skills in English.
• Strong health informatics and programming skills. Excellent programming skills in statistical packages such as SAS or R.
• Cognitive abilities including; verbal reasoning, attention to detail, critical thinking, and analytical ability.
• 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).

Additional Skills/Preferences:

• Epidemiology, clinical pharmacology, therapeutic area, or other medical and scientific specific knowledge and experience (e.g., neuroscience, immunology, oncology, or endocrine expertise).
• Expertise with clinical vocabularies, terminologies, or coding systems that are structured to represent the care and treatment of patients. Terms cover diagnoses, findings, operations, treatments, drugs, administrative items etc., with examples being SNOMED, ICD, CPT, RXNORM, etc.,.
• Expertise with external health data and information standards for the structure, processing, and delivery of health information. This includes the issues of information representation and interoperability between systems.
• Publication experience.
• Ability to work well independently and as part of a team.
• Limited travel, up to approximately 10%

Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively “Lilly”) are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources ( Lilly_Recruiting_Compliance@lists.lilly.com ) for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process. 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.