Job Description

Job Title: Clinical Research Coordinator (Oncology/Hematology)Location: SingaporeJob Summary: One of our clients is seeking a dedicated and detail-oriented Clinical Research Coordinator to join our team in the Oncology/Hematology therapeutic area. The ideal candidate will have a healthcare background and be passionate about contributing to cutting-edge clinical research. This role involves coordinating clinical trials, ensuring compliance with regulatory requirements, and providing support to the research team.Key Responsibilities:

• Assist Principal Investigators in the conduct of clinical trials and research studies, adhering to study protocols, Singapore Good Clinical Practice Guidelines, and other regulatory and ethical requirements.
• Coordinate patient recruitment, screening, and scheduling of trial-related procedures.
• Manage data entry, validation, and extraction of relevant information from medical records.
• Report adverse events and maintain investigator files and essential documentation.
• Prepare for and conduct cross-institution audits/inspections, ensuring safety and compliance at study sites.
• Support database establishment, migration, and maintenance.
• Organize and participate in departmental academic or service meetings, such as grand rounds, Tumor Boards, and journal clubs.
• Assist in preparing scientific manuscripts and presentations for scientific meetings or other study-related presentations.
• Provide general administrative support and coordination for research and academic activities as required.

• Degree in Life Sciences, Health Sciences, Nursing, Medicine, Pharmacy, or a related field.
• Prior experience in clinical research or clinical trials, particularly in Oncology or Hematology, is highly advantageous.
• Proficiency in Microsoft Office and statistical software.
• Excellent communication and interpersonal skills, with the ability to work both independently and as part of a team.
• Meticulous, proactive, and well-organized, with strong multitasking capabilities.
• Bilingual abilities are a plus.

• Knowledge of ICH Good Clinical Practice (GCP) guidelines.
• Experience with data management and regulatory submissions.
• Ability to empathize with patients and provide a smooth patient journey during clinical trials.

SL-Human Resource Consultancy Pte Ltd