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Clinical Research Coordinator, Paediatrics
1 month ago
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
Tell employers what skills you have
Data Analysis
Clinical Research
Public Health
Treatment
Healthcare
Invoicing
Administration
Clinical Operations
Clinical Trials
Protocol
Educational Materials
Preparedness
Interventions
Life Sciences
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