Clinical Research Coordinator (Haematology-Oncology) 1 year contract

Job ID:  1334
Job Function:  Allied Health
Institution:  National University Hospital


A clinical research coordinator will assist Principal Investigator or Co-investigators to monitor the administration and progress of a clinical trial.


You will be responsible for the following:

• Oversee overall clinical operations related to the conduct of the clinical trials.

• To adhere to compliance with Research Governance, Good Clinical Practice, Data Protection and Ethical Requirements.

• To ensure the study and study procedures are conducted in accordance with the study protocol

• To participate in patient recruitment.

• To ensure study entry criteria are fulfilled.

• To ensure informed consent procedure is followed.

• To coordinate patient visits for future tests and procedures.

• To schedule visit according to study protocol.

• To organize and participate in site initiation visit.

• To work in collaboration with study team to ensure trial preparedness.

• To monitor patients throughout the study to ensure study drugs are given according to protocol requirement.

• To arrange for clinical and laboratory investigations to be carried out according to protocol.

• Ensure results of investigations and X-ray films are collected.

• Maintains records of additional investigations for invoicing purposes.

• To collects and collates research data, ensuring its accuracy and completeness.

• Ensure timely and accurate transcription of information on source documents, paper case report forms (CRFs), or electronic CRFs.

• To label and ensure biological specimens are delivered in the correct conditions as specified in the trial protocol.

• To assist investigator(s) in adverse events / serious adverse events reporting.

• To maintain confidentiality on patient data.

• To work with pharmacy to maintain drug accountability logs.

• To raise payment request forms for billing to companies

• Creation and maintenance of all trial files, including the trial master file, and oversight of site files.

• To work with company in developing and implementing recruitment plan to ensure long-term recruitment target is met.



• Scientific qualification preferred but other suitable qualification will be considered on a case-by-case basis.

• Ability to work both independently and in a team.

• Good patient interaction skills.

• Be flexible and self-motivated.

• Ability to write clearly

• Possess excellent organisational skills.

• Enjoy paying attention to detail.

• Computer literacy


Interested applicants are invited to email a detailed resume stating your current and expected salary to