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Clinical Trials for Study Coordinators
Clinical Trials for Study Coordinators
Last date: October 17th & 18th, 2024
A clinical research coordinator is in charge of managing clinical research as per the protocol, ICH- GCP, and other regulatory needs. Primary responsibilities normally include administering questionnaires, informing the participants about the objectives of the study, collecting data, participate in recruitment of the subjects. and managing all the trials. Clinical research coordinators also have to explain the subjects the things that are expected during the trial and resolve any concerns. This means that a clinical research coordinator needs communicative and interpersonal skills.
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Home
About us
Our activities
Our Activities
Conferencing
Clinical Trials Symposium
Roundtables
Workshops
Training
Clinical Research Associate (CRA) Training Program – Entry & Advanced Level
Study nurses
ICH Good Clinical Practice (GCP) Training Program – Entry & Advanced Level
Clinical Trials for Investigators
Clinical Trials for Study Coordinators
Postgraduate course for Project Management in Clinical Trials
Clinical Trials Fundamentals for Life Science Graduates
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Consulting
Charity campaign
News
Partners
Contact