Job Description:
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 research activities at NUH:
· 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 interventions are given according to protocol requirement.
· To arrange for assessments to be carried out according to protocol.
· 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 assist investigator(s) in adverse events / serious adverse events reporting.
· To maintain confidentiality on patient data.
· To raise payment request forms for billing
· Creation and maintenance of all trial files, including the trial master file, and oversight of site files.
· To prepare and submit ethics (Domain Specific Research Board) reports
· To liaise with the collaborators (KK Women’s and Children’s Hospital, Saw Swee Hock School of Public Health, industrial company) for recruitment, interventions and data analysis
In addition to above research-related duties, you will also be involved in:
· Coordination with appointed vendor for the development and production of patient and healthcare provider educational materials on patient treatment modality
· Organisation of training workshops for healthcare providers.
Requirements:
· 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, and liaise with various parties
· Good patient interaction skills.
· 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, and liaise with various parties
· Good patient interaction skills
