Opportunity to work as Clinical Trial Project Manager at Lilly- Apply before 25th March 2025

About Lilly

At Lilly, we are committed to combining compassion with innovation to improve lives worldwide. Headquartered in Indianapolis, Indiana, we are a global healthcare leader dedicated to discovering and delivering life-changing medicines. Our mission extends beyond medicine, as we actively contribute to our communities through philanthropy and volunteerism. We believe in prioritizing people, and we seek individuals who share our passion for making a meaningful impact.

Job Title:

Clinical Trial Project Manager

Job Location:

Bangalore, Karnataka

Industry:

Pharmaceuticals / Healthcare / Clinical Research

Functional Area:

Research & Development

Application Deadline:

March 25, 2025

Role Overview

As a Clinical Trial Project Manager (CTPM) Associate, you will lead cross-functional study teams to execute clinical trials with quality, efficiency, and adherence to timelines and budgets. You will be responsible for project management, risk mitigation, trial execution, and cross-functional collaboration to ensure successful study completion.

Key Responsibilities

Project Management & Operational Oversight

• Develop and execute local, regional, and global clinical trials using project management methodologies.
• Define project scope, monitor trial status, and implement changes as needed.
• Create and track global trial enrollment plans, integrating inputs from multiple teams.
• Identify and mitigate trial-level risks with a proactive contingency plan.
• Oversee budget management, ensuring efficient resource allocation.
• Partner with affiliates, investigators, and third-party organizations (TPOs) to facilitate trial execution.
• Ensure timely trial delivery by coordinating with cross-functional teams.

Clinical Trial Process Leadership

• Demonstrate a thorough understanding of the drug development process and its impact on trial execution.
• Maintain inspection readiness by ensuring accurate documentation and compliance.
• Address operational challenges and implement process improvements to enhance efficiency.
• Serve as the central communication point between clinical development teams, external partners, and regulatory bodies.
• Oversee vendor qualification, selection, and management.

Scientific & Regulatory Expertise

• Provide scientific and regulatory insights for clinical and regulatory documentation.
• Support regulatory submissions and responses to agency inquiries.
• Collaborate with global and regional teams to ensure trial feasibility and compliance.
• Apply knowledge of Good Clinical Practice (GCP) and regulatory guidelines to trial execution.

Candidate Requirements

Educational Qualifications:

• Bachelor’s or Master’s degree in a scientific or health-related field.

Skills & Competencies:

• Strong project management skills with experience in clinical trial operations.
• Ability to influence stakeholders without direct authority.
• Excellent leadership, communication, and networking abilities.
• Problem-solving and critical-thinking skills to navigate complex situations.
• Experience working with global teams and third-party organizations.
• Proficiency in project management tools (e.g., MS Project, MS Excel, MS PowerPoint).
• Ability to manage priorities in a dynamic environment.

Preferred Qualifications:

• Previous experience in clinical trials, especially at site or affiliate levels.
• Understanding of regulatory requirements in global and regional contexts.
• Familiarity with risk management and contingency planning.
• Willingness to travel periodically for trial oversight.

Why Join Us?

At Lilly, we foster a collaborative and inclusive work environment where innovation thrives. By joining our team, you will have the opportunity to contribute to groundbreaking research, drive positive change in healthcare, and grow professionally in a dynamic global setting.

Apply Today!

If you are passionate about clinical research and committed to improving patient outcomes, we invite you to apply for this exciting opportunity.