Clinical Research Nurse — Study Coordinator & Patient Advocate

St. Luke's Medical Center; Quezon City; On-site; PHP 360,000 - 600,000; Full time

Job summary

St. Luke’s Medical Center in Quezon City is seeking a dedicated Research Nurse to coordinate clinical studies on-site. You will screen and enroll participants, obtain informed consent, administer study procedures, and monitor safety in collaboration with physicians and study teams.

The role emphasizes regulatory compliance, accurate documentation, and participation in meetings and quality improvement initiatives to advance patient-centered research.

Qualifications

• Assists investigator in assessing patients for protocol eligibility.
• Maintains source documentation and prepares study activity reports for sponsors and regulatory bodies as appropriate.
• Obtains pharmacology and other required laboratory specimens as required by protocols and safety standards.
• Serves as the R&B monitor for clinical trials / clinical research projects.
• Collaborates with multidisciplinary teams to monitor and evaluate patient and family response to the study.

Responsibilities

• Coordinating and implementing clinical research protocols, including patient screening, enrollment, informed consent, and follow-up visits.
• Collecting and documenting clinical data and administering study-related treatments according to protocol.
• Monitoring participants for safety and adherence; maintaining accurate records.
• Preparing reports or documentation for audits and study meetings; ensuring regulatory and ethical compliance.
• Participating in departmental meetings, training, and quality improvement initiatives; educating patients about study participation.

Job description

St. Luke’s Medical Center in Quezon City is seeking a dedicated Research Nurse to coordinate clinical studies on-site. You will screen and enroll participants, obtain informed consent, administer study procedures, and monitor safety in collaboration with physicians and study teams.

The role emphasizes regulatory compliance, accurate documentation, and participation in meetings and quality improvement initiatives to advance patient-centered research.