Clinical Research Coordinator (Nursing Research) (Contract)

Singapore General Hospital Pte Ltd.; Singapore; Híbrido; SGD 33 000 - 56 000; Tempo integral

Resumo da oferta

Singapore General Hospital is seeking a Clinical Research Coordinator I/II to support clinical and health services research in accordance with regulatory and protocol requirements. The role collaborates with the PI, department staff, sponsors, and monitors to ensure compliant administration of studies.

Responsibilities include day-to-day logistics, involvement in internal monitoring, budgeting, trainer for delegated staff, and preparation for audits/inspections.

Qualificações

• Bachelor’s degree in Life Science/Pharmacy or related field; Diploma holders also eligible.
• Nursing (on project basis) experience may be considered.
• Clinical Trial Management Diploma/Advance Diploma/ Degree preferred.
• Proficiency in MS Office with intermediate to advanced Excel skills.

Responsabilidades

• Manages research study independently; coordinates daily study activities with the team.
• Participates in evaluating study proposals and protocols.
• Understands assigned protocol, timelines, inclusion/exclusion criteria, and privacy protections.
• Assists PI in designing recruitment materials and essential study documents (CRFs, source docs).
• Supports study submissions to IRB/HSA and reports safety events as required.
• Compiles study results and performs simple statistical analyses.
• Assists in budget preparation and negotiations for trial agreements.
• Maintains study payment trackers and reimbursements for participants.

Conhecimentos

Project coordination

Healthcare experience

MS Excel

MS Office

Formação académica

Bachelor's or Diploma in Life Science/Pharmacy

Nursing (on project basis)

Clinical Trial Management Diploma/Advance Diploma/ Degree

Ferramentas

MS Office

Excel

Descrição da oferta de emprego

The Clinical Research Coordinator I/II provides research support service for clinical or health services research, in accordance with the applicable regulatory, Good Clinical Practice and protocol requirements. He/she works closely with the Principal Investigator (PI), members of the department, study sponsors and monitors, etc. to support and provide guidance on the administration of the compliance, financial, personnel and other related aspects of the clinical studies.

In addition, he/she ensures smooth and efficient day-to-day logistics support for research and innovation projects and assists in study quality control activities such as internal monitoring and prepares for auditing/ inspection.

The Clinical Research Coordinator supports and participates in the SGH Nursing Research and Innovation mission of providing quality patient care, education, research.

Responsibilities

• Manages research study independently. Acts as liaison between subjects and other members of the research team to facilitates and coordinates the daily research study activities.




• Participates in the evaluating of the study proposals and protocols.




• Comprehends each assigned protocol including study proceedings and timelines, inclusion and exclusion criteria, confidentiality and privacy protections.




• Assists PI in designing and development of study recruitment advertisement, study specific source documents/ Case Report Forms and other required documents pertaining to the protocol.




• Assists sponsor or PI in the study submission to IRB or HSA. Oversees all study subject-related issues, timely report all safety events according to sponsor, IRB and regulatory authorities’ requirements.

• Compiles study results in projects database and perform simple statistical analysis.




• Assists in budget preparation and facilitates clinical trial agreement discussion.




• Develops and maintains study payment tracker, prepares study participants payment reimbursement.




• Provides study protocol specific training to delegated staff with supervision of PI.




• Participates in and /or takes responsibility for tasks and activities which support the goals of the department and hospital.

Requirements

• Bachelor Degree in Life Science/ Pharmacy & any other relevant disciplines, or Diploma in




• Life /Pharmaceutical Science/Clinical Trial Management, Diploma /Advance Diploma/ Degree




• in Nursing (on project basis)




• Knowledge of MS Office software (Intermediate to Advanced Excel skills)




• Prior working experience in healthcare setting preferred




• Have experience managing and coordinating multiple projects

Please note that this will be a short-term contract position of 6 to 8 months.