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Clinical research coordinator, oncology/hematology

1 month ago

Singapore SL-Human Resource Consultancy Pte Ltd Full time

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.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.#J-18808-Ljbffr