Clinical Research Operations Manager (1-Year Contract) - Bali, Indonesia

Join JobStudio as a Clinical Research Operations Manager in the heart of Bali and lead groundbreaking healthcare initiatives that shape the future of medical innovation. This 1-year contract role offers a unique opportunity to oversee high-impact clinical research projects from start to finish. Based in Bali's vibrant research hubs, you'll work alongside a dynamic team of experts to ensure seamless operations and compliance with global standards.

As a Clinical Research Operations Manager at JobStudio, you'll be responsible for managing the day-to-day operations of clinical trials, coordinating with research sites, and ensuring all regulatory requirements are met. You'll have the chance to work with cutting-edge technologies and contribute to groundbreaking medical advancements. This is your opportunity to make a significant impact in the healthcare industry while enjoying Bali's unique lifestyle.

📋 Tanggung Jawab Pekerjaan

• Oversee the end-to-end management of clinical research projects, ensuring timely and efficient execution.
• Coordinate with research sites, CROs, and regulatory agencies to ensure compliance with global standards.
• Develop and implement operational strategies to optimize research processes and improve efficiency.
• Manage budgets and resources, ensuring financial compliance and cost-effectiveness.
• Conduct regular site audits to monitor quality and compliance.
• Collaborate with cross-functional teams to ensure seamless integration of research activities.
• Provide training and support to research staff to enhance their skills and knowledge.
• Stay updated with the latest trends and best practices in clinical research operations.

🎓 Kualifikasi & Syarat

• Bachelor's degree in a relevant field such as Pharmacy, Medicine, Public Health, or a related discipline.
• Minimum of 5 years of experience in clinical research operations, with a strong background in regulatory affairs.
• Proven experience in managing clinical trials from initiation to completion.
• Certification in Good Clinical Practice (GCP) or equivalent.
• Proficiency in clinical research software such as Oracle Clinical, Medidata Rave, or similar.
• Strong knowledge of regulatory requirements and compliance standards.
• Excellent leadership and project management skills.
• Ability to work effectively in a fast-paced, dynamic environment.

🛠️ Keahlian

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