Deskripsi Pekerjaan
Are you passionate about advancing medical science and improving patient outcomes? The Singapore Eye Research Institute (SERI) is seeking a dedicated Clinical Research Coordinator to join our dynamic team. In this critical role, you will assist principal investigators in executing rigorous clinical studies, ensuring that every participant receives the highest standard of care while contributing to valuable research data. We are looking for a detail-oriented professional who thrives in a fast-paced environment and is committed to the integrity of clinical trials.
As a Clinical Research Coordinator at SERI, you will play a pivotal role in the full research lifecycle, from initial study setup to participant follow-up. Your expertise will help drive our mission to prevent, treat, and cure eye diseases and visual impairment. We offer a collaborative culture where your contributions are valued and your professional growth is supported.
Tanggung Jawab
- Assist in the recruitment and screening of eligible participants for clinical trials and research studies.
- Conduct study-specific clinical procedures and medical assessments in strict compliance with Good Clinical Practice (GCP) and study protocols.
- Manage participant follow-up schedules, ensuring adherence to visit timelines and maximizing retention rates.
- Collect, verify, and enter accurate clinical data into study databases and electronic case report forms (eCRFs).
- Liaise effectively with study participants, investigators, and external partners to foster a collaborative research environment.
- Ensure all study documentation, including informed consents and medical charts, is maintained and up-to-date.
- Monitor study progress and report any adverse events or protocol deviations to the principal investigator immediately.
Kualifikasi
- Bachelor’s degree in Nursing, Life Sciences, Medicine, or a related field.
- Previous experience in clinical research coordination or the healthcare sector is highly preferred.
- Strong interpersonal and communication skills with the ability to build rapport with patients and medical staff.
- Excellent organizational skills and attention to detail when managing complex study timelines and data.
- Familiarity with Good Clinical Practice (GCP) guidelines is an advantage.
- Proficient in computer applications and data entry systems.
- Ability to work independently and collaboratively within a multidisciplinary team.