job description
Join Peregrine Eye and Laser Institute, a leading healthcare provider specializing in advanced ophthalmology and laser treatments, as our Clinical Research Coordinator in Bali, Indonesia. This is an exciting opportunity to contribute to groundbreaking clinical research while working in a dynamic, patient-centered environment. If you are passionate about medical research, regulatory compliance, and improving patient outcomes, we want you on our team!
As a Clinical Research Coordinator, you will play a pivotal role in managing clinical trials, ensuring adherence to protocols, and maintaining the highest standards of ethical and regulatory compliance. You will collaborate with cross-functional teams, including physicians, researchers, and regulatory bodies, to drive innovative research initiatives that shape the future of eye care.
Bali offers a unique blend of professional growth and a high quality of life, making it an ideal location for healthcare professionals. At Peregrine Eye and Laser Institute, we foster a supportive and inclusive work culture that values innovation, teamwork, and continuous learning. If you are ready to take your career to the next level in a tropical paradise, apply now!
Responsibility
- Coordinate and manage clinical research studies, ensuring compliance with protocols, ethical guidelines, and regulatory requirements.
- Recruit, screen, and enroll study participants while maintaining accurate and confidential records.
- Collaborate with principal investigators and research teams to develop study materials, including informed consent forms and case report forms.
- Monitor study progress, track data, and ensure timely submission of reports to regulatory bodies and sponsors.
- Conduct site visits, audits, and inspections to ensure adherence to Good Clinical Practice (GCP) standards.
- Facilitate communication between study sponsors, investigators, and participants to address any issues or concerns.
- Prepare and maintain study documentation, including regulatory submissions, study logs, and adverse event reports.
- Provide training and support to research staff on study protocols, procedures, and compliance requirements.
Qualifications
- Bachelor’s degree in Nursing, Life Sciences, Public Health, or a related field. A Master’s degree is a plus.
- Minimum of 2 years of experience in clinical research, healthcare, or a related field.
- Strong knowledge of Good Clinical Practice (GCP), ICH guidelines, and regulatory requirements for clinical trials.
- Excellent organizational, communication, and interpersonal skills.
- Ability to work independently and manage multiple priorities in a fast-paced environment.
- Proficiency in Microsoft Office Suite and clinical research management software.
- Fluency in English; additional languages (e.g., Bahasa Indonesia) are a plus.
- Certification in Clinical Research (e.g., SOCRA, ACRP) is highly desirable.