Clinical Research Coordinator - Healthcare & Medical

Join Singapore General Hospital as a Clinical Research Coordinator and play a pivotal role in advancing medical research in Bali. This is a unique opportunity to contribute to groundbreaking clinical projects while working in a dynamic and collaborative environment. In this role, you will manage the day-to-day operations of clinical trials, ensuring compliance with international standards and regulations. Based in Ubud, you'll be part of a team dedicated to improving patient care through innovative research.

As a Clinical Research Coordinator at Singapore General Hospital, you will be responsible for coordinating and managing clinical research studies from inception to completion. You will work closely with researchers, clinicians, and regulatory bodies to ensure the smooth execution of trials. This role offers a competitive salary and the chance to grow within a reputable healthcare organization.

📋 Tanggung Jawab Pekerjaan

• Manage the day-to-day operations of clinical trials, ensuring compliance with international standards and regulations.
• Coordinate with researchers, clinicians, and regulatory bodies to ensure the smooth execution of trials.
• Develop and maintain study documentation, including protocols, case report forms, and study reports.
• Monitor and report on trial progress, including recruitment, data collection, and adverse event reporting.
• Ensure the safety and well-being of study participants by adhering to ethical guidelines and regulatory requirements.
• Provide administrative support to the research team, including scheduling, travel arrangements, and vendor management.
• Collaborate with data management teams to ensure accurate and timely data entry and reporting.
• Participate in training and education programs to stay updated on best practices and regulatory changes.

🎓 Kualifikasi & Syarat

• Bachelor's degree in healthcare administration, public health, or a related field.
• Minimum of 3 years of experience in clinical research coordination or a related role.
• Certification in clinical research coordination (CRC) or a related certification is preferred.
• Proficiency in English, both written and spoken.
• Strong organizational and project management skills.
• Experience with clinical trial management software such as Oracle Clinical, Medidata Rave, or similar.
• Knowledge of international regulatory requirements, including ICH-GCP and FDA regulations.
• Ability to work independently and as part of a team in a fast-paced environment.

🛠️ Keahlian

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