Clinical Research Coordinator (Healthcare/ Pharmaceutical, Data))

• The Clinical Research Coordinator will be responsible for coordinating and participating in  clinical research studies conducted by principal investigator(s) in the department. 
• The Clinical Research Coordinator will coordinate and participate in a variety of complex activities involved in the collection, compilation, documentation and analysis of clinical research data. 
• The ideal Clinical Research Coordinator will be expected to-
• Coordinate and participate in clinical research studies conducted by principal investigator(s), collect, complete, document, and analyze clinical research data
• Implement procedures to collect data from patient charts, medical records, interviews, questionnaires, diagnostic tests and other sources
• Evaluate and interpret collected clinical data in conjunction with principal investigator(s) as appropriate
• Prepare presentations and reports that show progress, trends, recommendations, and/or bconclusions
• Develop forms, questionnaires and applications of research techniques

Requirements

• Min Degree, preferably in Science / Life Sciences / Public Health / Health Sciences / Pharmacy / Medicine / Nursing or similar from an accredited university
• At least 1-2 years of working experience within clinical research settings (e.g. clinical research associate, study coordinator, or research administrator) is advantageous but not essential
• Knowledge of GCP guidelines and applicable regulations and guidelines of clinical research, or ethical principles relating to human biomedical research
• Able to work independently, as well as part of a team
• Able to work with a high degree of accuracy and attention to detail
• Possess excellent analytical, organisation, communication, and interpersonal skills

If you are interested in the position, do kindly drop your most updated resume to [Click Here to Email Your Resume]  (Attn: Clinical Research Coordinator - Leon)

Thank You.

Leon Leong De Cong
R1551708

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