Clinical Research Coordinator
2 weeks ago
Job Description:
You will be responsible for the following:
a) To adhere to compliance with Research Governance, Good Clinical Practice, Data Protection and Ethical Requirements.
b) To ensure the study and study procedures are conducted in accordance with the study protocol.
c) To participate in patient recruitment.
d) To ensure informed consent procedure is followed.
e) To coordinate patient visits for future tests and procedures.
f) To organize and participate in site initiation visits.
g) To arrange for clinical and laboratory investigations to be carried out according to protocol.
h) To collect and collates research data, ensuring its accuracy and completeness.
i) Ensure timely and accurate transcription of information on source documents, paper case report forms (CRFs), or electronic CRFs.
j) To label and ensure biological specimens are delivered in the correct conditions as specified in the trial protocol.
k) To assist investigator(s) in adverse events / serious adverse events reporting.
l) Creation and maintenance of all trial files, including the trial master file, and oversight of site files.
Requirements:
a) Science-related qualifications are preferred but degrees in other fields will be considered as well.
b) Ability to work both independently and in a team.
c) Good communication skills. Ability to speak Mandarin and common local dialects will be an added advantage.
d) Good patient interaction skills.
e) Be flexible and self-motivated.
f) Ability to write clearly
g) Possess excellent organisational skills.
h) Enjoy paying attention to detail.
i) Computer literacy.
j) Ability to work flexibly with occasional weekends and late nights.
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