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Associate/Clinical Research Coordinator (with Radiography experience) - PHR job in Singapore at SINGAPORE EYE RESEARCH INSTITUTE

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Associate/Clinical Research Coordinator (with Radiography experience) - PHR at SINGAPORE EYE RESEARCH INSTITUTE

Associate/Clinical Research Coordinator (with Radiography experience) - PHR

SINGAPORE EYE RESEARCH INSTITUTE Singapore Contract

The SINGAPORE EYERESEARCH INSTITUTE (SERI) serves as Singapore’s national research institute for ophthalmic and vision research. SERI functions as the research arm of the various clinical ophthalmic centres in Singapore including the Singapore National Eye Centre, the National University Health Systems (NUHS), Tan Tock Seng Hospital etc., and further works in collaboration with Duke-NUS Graduate Medical School and various biomedical research institutions, as well as major eye centers and research institutes throughout the world. SERI has developed aworld-leading reputation in broad-based clinical translational research and epidemiological programmes for many eye diseases, particularly disease relevant to Asia. SERI currently has close to 200 staff with an annual budget of $20M.

Job Description

  • Oversee the planning, scheduling and carrying out of day-to-day research activities and procedures
  • Perform Dual Energy X-Ray Absorptiometry (DXA) machine, to collect bone mineral density (BMD) and body composition (BC) measures using DXA
  • Coordinate recruitment, study screening, and follow up visits of research subjects
  • Collect clinical, DXA and patient-related data
  • Maintain Investigator Site File (ISF) and update screening log and enrolment logs
  • Ensure all clinical activities are carried out and complied in accordance with established research protocols and standards
  • Any ad-hoc duties as assigned by supervisor

Job Requirements

  • Recognized Diploma or Degree in Radiography
  • Relevant experience in operating Dual Energy X-Ray Absorptiometry (DXA) machine, and in performing bone mineral density (BMD) and body composition (BC) examinations using DXA
  • Possess full registration from AHPC
  • Strong communication and interpersonal skills, leadership and people management skills
  • Must be able to work independently in a dynamic environment
  • Experience administering survey questionnaires and collecting clinical data from study participants
  • Computer competency including proficiency in MS Office (Word, Excel, PowerPoint)
  • Ability to manage multiple projects simultaneously and effectively work in teams
  • Have a pleasant and engaging demeanour

Note: Package will commensurate with qualifications and experience

 

Recommended Skills

  • Pre Clinical Development
  • Clinical Study Design
  • Medical Writing
  • Drug Development
  • Clinical Trials
  • Electronic Common Technical Document
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Job ID: 2_69e9402c4e563a9710f20fbbf9aae1

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