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Jobs in Singapore   »   Jobs in Singapore   »   Education / Training Job   »   Clinical Research Coordinator (Contract)
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Clinical Research Coordinator (Contract)

National University Hospital (singapore) Pte Ltd

National University Hospital (singapore) Pte Ltd company logo

Job Purpose

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

Duties and Responsibilities

Primary Duties and Responsibilities


Clinical Trial

  • 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.

Secondary Duties and Responsibilities


Recruitment Plan

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

Job Specification/Requirements

  • Life science diploma/ degree or nursing degree is preferred. The relevant degree subject area is life science or biomedical science.
  • Ability to work both independently and in a team.
  • Good communication skills.
  • Good patient interaction skills.
  • Be flexible and self-motivated.
  • Ability to write clearly
  • Possess excellent organisational skills.
  • Enjoy paying attention to detail.
  • Computer literacy.
  • Ability to work flexibly with occasional weekends and late nights.

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