Clinical Research Coordinator - Leading Healthcare Innovation in Bali
Join Mandaya Hospital Group, a pioneer in healthcare excellence, as a Clinical Research Coordinator in the vibrant heart of Bali. This is a unique opportunity to contribute to groundbreaking clinical studies that shape the future of medical research while working in a dynamic and supportive environment. As part of our team, you'll be at the forefront of clinical research, ensuring the smooth execution of studies and the highest standards of patient care.
In this role, you'll manage the day-to-day operations of clinical trials, coordinate with researchers, and ensure compliance with regulatory requirements. You'll work closely with a team of healthcare professionals to deliver exceptional research outcomes. This is your chance to make a meaningful impact in the healthcare industry while enjoying the beauty and culture of Bali.
Mandaya Hospital Group is committed to fostering a culture of innovation and excellence. With state-of-the-art facilities and a team of dedicated professionals, we provide an ideal setting for you to grow and succeed. Join us and be part of a team that is shaping the future of healthcare.
๐ Tanggung Jawab Pekerjaan
- Manage the day-to-day operations of clinical trials, ensuring adherence to study protocols and regulatory guidelines.
- Coordinate with researchers, clinicians, and other stakeholders to ensure the smooth execution of clinical studies.
- Monitor and report study progress, including patient recruitment, data collection, and adverse event reporting.
- Ensure compliance with ethical and regulatory standards, including GCP (Good Clinical Practice) guidelines.
- Develop and maintain study-related documentation, including Case Report Forms (CRFs) and Informed Consent Forms (ICFs).
- Collaborate with the data management team to ensure accurate and timely data entry and reporting.
- Provide support to the clinical team in patient care and study-related activities.
- Participate in continuous quality improvement initiatives to enhance the efficiency and effectiveness of clinical research processes.
๐ Kualifikasi & Syarat
- Bachelor's degree in Life Sciences, Pharmacy, Medicine, or a related field.
- Minimum 3 years of experience in clinical research coordination or a related role.
- Strong understanding of clinical research principles and regulatory requirements, including GCP and ICH-GCP.
- Proficient in using clinical research software such as OpenClinica, Medidata Rave, or similar platforms.
- Excellent organizational and time management skills.
- Strong communication and interpersonal skills, with the ability to work effectively in a team environment.
- Ability to work under pressure and meet tight deadlines.
- Fluent in English, both written and spoken.
๐ ๏ธ Keahlian
Kirim lamaran sekarang sebelum batas waktu.๐ Lamar Sekarang