job description
Are you passionate about advancing clinical research and making a tangible impact on healthcare outcomes? Woodlands Health is seeking a dedicated Clinical Research Coordinator to join our dynamic team in Bali. In this role, you will play a pivotal part in managing and facilitating clinical studies, ensuring compliance with regulatory standards, and contributing to groundbreaking medical research.
Based in the vibrant and culturally rich environment of Bali, this position offers a unique opportunity to blend professional growth with an exceptional quality of life. You will collaborate with a multidisciplinary team of healthcare professionals, researchers, and administrators to drive forward our mission of improving patient care through evidence-based research.
If you are detail-oriented, organized, and eager to contribute to meaningful healthcare advancements, we invite you to apply and become a part of our innovative research community.
Responsibility
- Coordinate and manage clinical research studies from initiation to completion, ensuring adherence to protocols and regulatory requirements.
- Liaise with principal investigators, study sponsors, and ethical review boards to facilitate study approvals and amendments.
- Oversee participant recruitment, screening, and enrollment, ensuring informed consent processes are followed meticulously.
- Maintain accurate and up-to-date study documentation, including case report forms, source documents, and regulatory binders.
- Monitor study progress, identify potential issues, and implement corrective actions to ensure timely and high-quality data collection.
- Conduct regular site visits and audits to ensure compliance with Good Clinical Practice (GCP) guidelines and study protocols.
- Prepare and submit progress reports, adverse event reports, and other required documentation to regulatory authorities and sponsors.
- Collaborate with data management teams to ensure the integrity and accuracy of study data.
Qualifications
- Bachelor's degree in Life Sciences, Nursing, Public Health, or a related field. A Master's degree is a plus.
- Minimum of 2 years of experience in clinical research coordination, preferably in a healthcare or academic setting.
- Certification in Good Clinical Practice (GCP) is highly desirable.
- Strong understanding of clinical trial methodologies, regulatory requirements, and ethical considerations.
- Excellent organizational and project management skills, with the ability to manage multiple studies simultaneously.
- Proficient in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Exceptional communication and interpersonal skills, with the ability to work effectively in a multicultural team.
- Fluency in English is required; proficiency in Bahasa Indonesia is an advantage.