Instagram
youtube
Facebook

Clinical Trial Project Manager

3+ years
Not Disclosed
10 Feb. 17, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

Clinical Trial Project Manager – Research & Development
Location: Bangalore, Karnataka, India
Job Type: Full Time Regular
Job Id: R-79410

Job Summary:
At Lilly, we unite caring with discovery to make life better for people around the world. As a Clinical Trial Project Manager (CTPM) Associate, you will lead cross-functional teams to develop and execute clinical trials, ensuring quality, on-time delivery, and adherence to scope and budget. This role requires project management expertise, clinical trial process leadership, and scientific knowledge to achieve successful trial outcomes.

Key Responsibilities:

  • Project Management & Regional Operational Knowledge:

    • Use project management tools and processes to execute clinical trials regionally and globally.
    • Monitor trial progress and adjust plans as needed to ensure successful trial completion.
    • Develop trial enrollment strategies and coordinate across functions for efficient execution.
    • Manage the trial budget, track expenses, and ensure financial alignment with stakeholders.
    • Partner with various organizations for affiliate, site, and investigator training.
    • Act as the central point of contact for trial communication and resolve issues effectively.
    • Identify and develop improvement activities based on industry trends.
  • Clinical Trial Process Leadership & Expertise:

    • Understand the drug development process and coordinate cross-functional activities.
    • Ensure trial records are compliant and inspection-ready.
    • Lead teams through complex issues and propose solutions to mitigate risks.
    • Apply global/regional regulations and Lilly standards in trial execution.
  • Scientific Expertise:

    • Use scientific knowledge to prepare clinical and regulatory documents.
    • Provide consultation on trial design, feasibility, and implementation.
    • Support the scientific needs of the business through critical thinking and problem-solving.

Minimum Qualification Requirements:

  • Bachelor’s degree (scientific or health-related preferred).
  • Applied knowledge of project management methodology and tools.
  • Experience in clinical trial management or a related field.
  • Strong leadership, communication, and organizational skills.
  • Ability to work cross-functionally with global teams and external partners.

Other Preferences:

  • Clinical trial experience with a strong understanding of the clinical research process.
  • Proficiency with project management tools (e.g., MS Project, MS Excel, MS PowerPoint).
  • Ability to travel periodically.

Lilly is committed to diversity and equal opportunity for all applicants. We encourage individuals with disabilities to apply.