job description
Join Eli Lilly and Company, a global leader in pharmaceutical innovation, as our Manager - Clinical Research Unit (CRU) Operations in Bali, Indonesia. In this pivotal role, you will oversee the day-to-day operations of our Clinical Research Unit, ensuring seamless execution of clinical trials while fostering cross-functional collaboration with medical, scientific, and operational teams.
As the CRU Operations Manager, you will play a critical role in advancing Lilly’s mission to deliver life-changing medicines to patients worldwide. You’ll lead a high-performing team, optimize operational workflows, and maintain compliance with global regulatory standards. This position offers a unique opportunity to contribute to groundbreaking research while working in a dynamic, fast-paced environment.
Bali’s vibrant culture and growing healthcare ecosystem make it an ideal location for professionals seeking a balance between career growth and quality of life. If you are a strategic leader with a passion for clinical research and operational excellence, we invite you to be part of our global team.
Why Join Eli Lilly?
- Work with a globally respected pharmaceutical company at the forefront of medical innovation.
- Opportunities for professional development and career advancement in a supportive environment.
- Competitive compensation package, including health benefits and performance incentives.
- Collaborate with cross-functional teams in a mission-driven culture focused on patient impact.
Responsibility
- Oversee daily operations of the Clinical Research Unit (CRU), ensuring adherence to protocols, timelines, and regulatory requirements.
- Lead and mentor a multidisciplinary team, fostering a culture of collaboration, accountability, and continuous improvement.
- Develop and implement operational strategies to enhance efficiency, quality, and compliance in clinical trial execution.
- Collaborate with medical, scientific, and operational stakeholders to align CRU activities with broader clinical development goals.
- Monitor and report on key performance indicators (KPIs) to senior management, identifying risks and proposing mitigation strategies.
- Ensure compliance with Good Clinical Practice (GCP), local regulations, and Lilly’s global standards for clinical research.
- Manage budgetary and resource allocation for CRU operations, optimizing costs without compromising quality.
- Drive process improvements and innovation in CRU workflows to support scalable and sustainable operations.
Qualifications
- Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or a related field; advanced degree (Master’s or PhD) preferred.
- Minimum 5 years of experience in clinical research operations, with at least 2 years in a managerial or leadership role.
- Proven track record in clinical trial management, CRU operations, or clinical site management.
- Strong understanding of Good Clinical Practice (GCP), ICH guidelines, and local regulatory requirements.
- Exceptional leadership skills with the ability to motivate teams, resolve conflicts, and drive performance.
- Excellent project management, organizational, and problem-solving abilities.
- Proficiency in English; additional languages (e.g., Bahasa Indonesia) are a plus.
- Experience with clinical trial management systems (CTMS) and electronic data capture (EDC) platforms is highly desirable.