Clinical Research Coordinator, Oncology/Hematology
2 months ago
Job Title: Clinical Research Coordinator (Oncology/Hematology)
Location: Singapore
Job 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.
Qualifications:
- 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.
Preferred Skills:
- 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.
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