Clinical Research Coordinator (Contract, Dept of Genomic Medicine)
Join KK Women's and Children's Hospital as a Clinical Research Coordinator in the Department of Genomic Medicine. This is a unique opportunity to contribute to groundbreaking research in genomic medicine while working in a dynamic and collaborative environment. As a Clinical Research Coordinator, you will play a pivotal role in coordinating clinical trials, ensuring compliance with regulatory requirements, and managing research data. Based in Canggu, you'll be part of a team dedicated to advancing genomic medicine, with access to state-of-the-art facilities and resources.
In this role, you'll work closely with researchers, clinicians, and administrative staff to design, implement, and monitor clinical trials. You'll use tools like REDCap for data management and ensure all processes adhere to Good Clinical Practice (GCP) guidelines. This position offers a competitive salary and the chance to work in a supportive and innovative research environment.
If you're passionate about genomic medicine and eager to make a significant impact, this is the perfect opportunity to join KK Women's and Children's Hospital and contribute to cutting-edge research in Canggu.
📋 Tanggung Jawab Pekerjaan
- Coordinate and manage clinical trials from inception to completion.
- Ensure compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines.
- Manage research data using REDCap and other relevant software.
- Collaborate with researchers, clinicians, and administrative staff to design and implement clinical trials.
- Monitor and report on trial progress and outcomes.
- Maintain accurate and up-to-date documentation of all trial activities.
- Provide administrative support to the research team.
- Assist in the preparation of regulatory submissions and reports.
🎓 Kualifikasi & Syarat
- Bachelor's degree in a relevant field such as Biology, Medicine, or Clinical Research.
- Minimum of 3 years of experience in clinical research coordination.
- Certification in Good Clinical Practice (GCP) or related field.
- Proficient in using REDCap and other clinical research software.
- Strong organizational and project management skills.
- Excellent communication and interpersonal skills.
- Ability to work independently and as part of a team.
- Familiarity with regulatory requirements for clinical trials.
🛠️ Keahlian
Kirim lamaran sekarang sebelum batas waktu.🚀 Lamar Sekarang