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Clinical Trial Project Manager

5-8+ years
Not Disclosed
10 Feb. 25, 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: Associate, Clinical Trial Project Manager (CTPM)

Location: Bangalore, Karnataka, India
Category: Research & Development
Job Type: Full Time Regular
Job ID: R-79410


About Eli Lilly:

At Eli Lilly, we unite caring with discovery to make life better for people around the world. As a global healthcare leader headquartered in Indianapolis, Indiana, we are committed to discovering life-changing medicines, improving disease management, and giving back to communities. We are seeking determined individuals who want to make a real difference in the world.


Purpose of the Role:

The Clinical Trial Project Manager (CTPM) Associate will lead the cross-functional study team in the development and execution of clinical trials. This role is responsible for ensuring the delivery of trials with quality, on time, within scope, and budget, while leveraging project management skills, regional operational knowledge, and clinical trial process expertise.


Key Responsibilities:

  1. Project Management & Operational Knowledge:

    • Understand the scope, monitor trial progress, and manage changes to meet deliverables.

    • Develop and track global trial enrollment plans, ensuring alignment across functions and geographies.

    • Identify and mitigate trial-level risks and oversee trial budgets using financial tracking tools.

    • Coordinate with local, regional, and global teams for training and execution of trials.

    • Serve as the single point of contact for trial communication between clinical development, CDDA, and third-party organizations (TPOs).

  2. Clinical Trial Process Leadership:

    • Maintain inspection readiness for the Trial Master File (TMF) and ensure quality in trial documentation.

    • Anticipate trial issues and propose proactive solutions to mitigate risks.

    • Lead and influence the team through ambiguity and coach team members on clinical trial processes.

  3. Scientific Expertise:

    • Leverage scientific and regulatory knowledge to consult on clinical and regulatory documents.

    • Apply clinical development and operational knowledge to impact trial design and implementation.


Minimum Qualifications:

  • Education: Bachelor’s or advanced degree in a scientific or health-related field.

  • Experience: Applied knowledge of project management processes and clinical trial experience.

  • Strong leadership and networking skills.

  • Excellent communication, self-management, and organizational skills.

  • Ability to manage complex situations and navigate ambiguity.


Additional Preferences:

  • Clinical trial experience with strong working knowledge of the clinical research process.

  • Experience with project management tools (e.g., Critical Chain, MS Project, Excel, PowerPoint).

  • Ability to travel periodically.


Equal Opportunity Employer:

Eli Lilly is committed to providing equal employment opportunities for all individuals, regardless of age, race, religion, gender, sexual orientation, disability, or any other legally protected status.


How to Apply:
For more information or to apply, please visit
Eli Lilly Careers.

Contact:
If you need accommodations during the application process, please complete the
accommodation request form.


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