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Https://Careers.Lilly.Com/Us/En/Job/Lillusr79410externalenus/Clinical-Trial-Project-Manager?Utm_Source=Indeed&Utm_Medium=Phenom-Feeds

5+ years
Not Disclosed
10 Feb. 4, 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 (CTPM) Associate

Location: Bangalore, Karnataka, India
Job Type: Full Time, Regular
Job ID: R-79410

About Lilly:

At Lilly, we unite caring with discovery to improve the lives of people worldwide. As a global healthcare leader, we are committed to discovering and delivering life-changing medicines to those in need, enhancing the understanding and management of diseases, and giving back to communities. We are looking for individuals passionate about making a positive impact.

Position Overview:

The Clinical Trial Project Manager (CTPM) Associate leads cross-functional teams in the development and execution of clinical trials, ensuring quality, timely delivery, and adherence to scope and budget. The CTPM Associate uses project management skills, regional operational knowledge, and clinical expertise to oversee trial execution and collaborate with other teams to meet key milestones.

Primary Responsibilities:

  • Project Management:
    • Manage trial scope, timeline, risk, and budget, ensuring alignment across regions and functions.
    • Assess risks and create mitigation plans, incorporating scientific knowledge and trial processes.
    • Track trial enrollment, working with cross-functional teams and monitoring the trial’s financial status.
    • Coordinate cross-functional study teams for smooth trial execution and resolution of issues.
  • Clinical Trial Leadership:
    • Coordinate and ensure inspection readiness for trial Master File (TMF) records.
    • Anticipate and address trial and regional issues, and propose proactive solutions.
    • Lead and influence teams to ensure adherence to regulatory and GCP standards.
  • Scientific Expertise:
    • Provide scientific consultation for regulatory documents and respond to queries from regulatory agencies.
    • Support trial design, feasibility, and implementation with knowledge of scientific and regulatory requirements.

Minimum Qualifications:

  • Education: Bachelor’s degree in a scientific or health-related field (advanced degree preferred).
  • Skills:
    • Strong knowledge of project management methodologies and tools (e.g., MS Project, Excel, PowerPoint).
    • Demonstrated ability to work cross-culturally and influence without authority.
    • Leadership skills with experience in cross-functional and cross-cultural teams.
    • Effective communication, problem-solving, and organizational skills.
  • Experience:
    • Clinical trial experience, especially in clinical research and site-level operations.
    • Prior experience in managing clinical trials, including working with external partners.

Other Preferences:

  • Familiarity with project management tools and techniques (e.g., Critical Chain).
  • Flexibility to adjust to shifting priorities and travel as needed.

Lilly’s Commitment to Diversity:

Lilly is dedicated to providing equal opportunities and fostering an inclusive work environment for all employees. We offer reasonable accommodations to individuals with disabilities during the application process.