job description
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. Based in Bali, you will play a pivotal role in coordinating and conducting research activities that aim to advance medical knowledge and improve patient outcomes.
As a Clinical Research Coordinator, you will work closely with a team of dedicated professionals, including researchers, clinicians, and administrative staff. Your role will involve managing various aspects of clinical research projects, ensuring compliance with ethical and regulatory standards, and facilitating the smooth execution of research protocols.
This contract position offers a competitive salary and the chance to be part of a prestigious institution known for its commitment to excellence in healthcare and research. If you are passionate about genomic medicine and have a keen interest in clinical research, we invite you to apply and be part of our mission to make a difference in the lives of women and children.
Responsibility
- Coordinate and manage clinical research projects in the Department of Genomic Medicine.
- Ensure compliance with ethical and regulatory standards for clinical research.
- Recruit and screen potential research participants, obtaining informed consent.
- Collect, process, and maintain accurate research data and documentation.
- Liaise with researchers, clinicians, and administrative staff to facilitate project execution.
- Prepare and submit research reports and documentation to relevant authorities.
- Monitor project timelines and budgets, ensuring adherence to established protocols.
- Provide support and training to research staff and participants as needed.
Qualifications
- Bachelor's degree in a relevant field such as Life Sciences, Nursing, or Public Health.
- Previous experience in clinical research coordination or a related role.
- Knowledge of clinical research regulations and ethical guidelines.
- Strong organizational and project management skills.
- Excellent communication and interpersonal skills.
- Ability to work independently and as part of a team.
- Proficiency in data management and documentation.
- Familiarity with genomic medicine and related research methodologies is a plus.