Instagram
youtube
Facebook

Principal/ Statistical Programmer

0-2 years
Not Disclosed
10 Feb. 18, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Principal/Statistical Programmer

Location: Bangalore, Karnataka, India
Category: Research & Development
Job Type: Full-Time, Regular
Job ID: R-64916


About Eli Lilly and Company:

At Eli 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 worldwide work to discover and bring life-changing medicines to those in need, improve disease management, and give back to communities through philanthropy and volunteerism. We're looking for individuals who are determined to make life better for people everywhere.


Job Description:

Key Responsibilities:

  • Programming Activities:

    • Support programming activities for clinical trial data analysis.

    • Create standard datasets (SDTM) and analysis datasets (ADaM).

    • Generate reports including Tables, Listings, and Graphs for clinical trials.

    • Support documentation tasks such as Define, RGs, and CRT packages.

  • Collaboration and Input:

    • Collaborate with statistical colleagues and study personnel on statistical analysis plans.

    • Select statistical methods for data analysis and author related sections of the analysis plan.

    • Conduct data analysis once the reporting database is created.

  • Data Quality and Assurance:

    • Work with data management to plan and implement data quality assurance plans.

  • Technology Proficiency:

    • Maintain proficiency in SAS programming and statistical methodology.

    • Justify selected methods and implement analysis plans effectively.

    • Peer-review work products from statistical colleagues.

  • Reporting and Communication:

    • Collaborate to write reports and communicate results of clinical trials.

    • Assist in regulatory submissions and manuscripts.

    • Respond to regulatory queries in collaboration with statistical colleagues.

  • Therapeutic Area Knowledge:

    • Understand relevant disease states to improve customer focus and collaboration.

    • Stay updated with advances in technology related to clinical trial analysis.

  • Regulatory Compliance:

    • Perform work in full compliance with corporate, medical, local, and departmental policies and procedures.


Minimum Qualifications:

  • Proficient in SAS programming and statistical methodologies.

  • Strong ability to collaborate with statistical colleagues and study teams.

  • Ability to effectively manage and communicate data analysis and results.

  • Bachelor's degree or higher in a relevant field.

  • Strong analytical, communication, and organizational skills.


Equal Opportunity Employer:

Eli Lilly is dedicated to providing equal employment opportunities for all individuals, including those with disabilities. If you need accommodation during the application process, please visit Workplace Accommodation for support. Lilly does not discriminate on the basis of age, race, religion, gender, sexual orientation, disability, or any other legally protected status.


How to Apply:

Interested candidates can apply directly via Lilly's career portal