The Associate / Research Coordinator will assist the Principal Investigator with population health studies using electronic health records and cancer registries. You will also help implement and coordinate research projects and its activities. These activities may include screening, recruitment and consent taking, incident event reporting, data collection and data management, biological specimen collection and retrieval, maintenance of site files and research participants’ follow up. You are required to adhere to Good Clinical Practice (GCP) guidelines, protocols, and regulatory compliances and also support the department with general administration tasks.
Requirements:
- Degree/Diploma in Life Science or its equivalent.
- Research experience will be an added advantage.
- Proficient in Microsoft Office applications.
- Proficient in English and a second language for ease of communication during patient recruitment.
- Good interpersonal and communication skills; comfortable interacting with patients, doctors, nurses, and other healthcare professionals.
- Meticulous, a good team player, independent and self-motivated with good time management abilities.
