Eli Lilly and Company Hiring Associate, Clinical Trial Project Manager (CTPM) | Bangalore, India

Eli Lilly and Company Hiring Associate, Clinical Trial Project Manager (CTPM)

Overview

Eli Lilly and Company, a global healthcare leader, is hiring an Associate, Clinical Trial Project Manager (CTPM) in Bangalore, Karnataka, India. If you have experience in project management within clinical trials and a background in life sciences, clinical research, or related fields, this could be your next career opportunity!

About Eli Lilly and Company

Eli Lilly and Company is committed to making life better through innovation and high-quality pharmaceuticals. Headquartered in Indianapolis, Indiana, the company has a strong presence worldwide, focusing on research, development, and improving global healthcare.

Job Role: Associate, Clinical Trial Project Manager (CTPM)

The Clinical Trial Project Manager (CTPM) Associate will lead cross-functional teams to execute clinical trials successfully. This role requires expertise in clinical trial project management, risk assessment, budgeting, and regulatory compliance.

Responsibilities

Project Management & Execution

• Develop and execute local, regional, and global clinical trials using project management tools and methodologies.
• Scope & Timeline Management: Monitor project scope and timelines, ensuring trials are delivered on time.
• Risk Mitigation & Contingency Planning: Identify trial risks and develop proactive strategies.
• Budget Tracking: Manage trial-level budgets and financial tracking tools.

Stakeholder & Team Coordination

• Lead cross-functional study teams throughout trial execution.
• Manage relationships with affiliates, investigators, and third-party organizations (TPOs).
• Oversee training programs for affiliates and site teams.

Regulatory & Clinical Compliance

• Ensure regulatory compliance with Good Clinical Practice (GCP) and industry regulations.
• Maintain trial inspection readiness and ensure adherence to clinical documentation processes.
• Collaborate with regulatory agencies, providing scientific and technical expertise.

Qualifications & Experience

Required Education

• Bachelor’s or Master’s degree in Life Sciences, Clinical Research, Pharmacy, Biotechnology, or related fields.

Experience & Skills

• Clinical trial management experience with knowledge of global and regional regulatory requirements.
• Strong project management skills, including budgeting, timeline tracking, and risk mitigation.
• Excellent communication, leadership, and stakeholder management abilities.
• Proficiency in MS Excel, MS PowerPoint, and project management tools.

How to Apply

Interested candidates can apply directly through the Eli Lilly Careers Portal.

👉 Apply Now

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