Clinical Research Coordinator

2-5 years
3500 - 4500 SGD monthly
22 days ago 1 Applied
Job Description

Community-based Oral Care Programme for Vulnerable Seniors through Tele-dentistry

Responsibilities

You will assist the principal investigator to develop and implement the tele-dentistry supported community-based oral care programme for seniors which includes:

. Key conduit between National Dental Centre Singapore (NDCS), Ministry of Health, SingHealth Regional Health System (RHS), Agencies, community partners.

. Prepare documents for and facilitate regulatory (e.g. Institution Review Board, Health Sciences Authority) approvals.

. Facilitate the signing of project agreements with external collaborators.

. Provide advice on programme implementation and workflow.

. Facilitate programme-related outreach events and training sessions.

. Design and develop informed consent form, data collection forms, logs and other study related document.

. Execute the approved clinical research protocols in accordance to the ICH-Guideline for Good Clinical Practice (ICH-GCP), Human Biomedical Research Act (HBRA) and other regulatory requirements, including (but not limited to) assisting the principal investigator(s) in:

  • Subject's consent taking
  • Scheduling study-related appointments for research subjects
  • Collect study data
  • Completing data collection forms
  • Administer surveys or questionnaires
  • Managing the study-related equipment
  • Handling queries by research subjects
  • Other patient-fronting research activities stated in the protocol

. Set up and maintain Investigator study file(s), including records of all approvals and reports.

. Coordinate and take minutes for study specific meetings between the various stakeholders such as NDCS, RHS and community partners.

. Set up and entry of research data into the study database.

. Simple interim analysis of data.

. Coordinating and taking notes for study specific meetings between the investigators and their study team members

. Ensure timely preparation and submission of study progress reports

. Preparation for study audits by relevant regulatory authorities and grant funding bodies

Requirements

. Degree in Nursing, Biological Science, Pharmacy or other healthcare related discipline.

. Familiar with Singapore Guideline for Good Clinical Practice (SGGCP), ethics and regulatory requirements for conducting clinical research

. Advanced knowledge of Microsoft Excel, and bio-statistical software applications.

. Excellent interpersonal and communication skills

. Strong verbal and written communication skills

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