Graduate / Post Graduate in Life Sciences / Clinical Research
Acting as the focal point of communication between the Investigator, Sponsor and study team.
Responsible for scheduling appointments effectively, and managing conflicts if any
Responsible for creating and updating study subjects electronic health records, source documents, master files.
Managing custody, circulation, control, retention and secure disposal of confidential information.
Arranging / scheduling clinical visits of patient
Comply with all SOPs, regulations, Good Clinical and Ethical Practices.
Screen, recruit and enroll eligible subjects and monitor their status.
Coordinating clinical trial with safety, integrity and efficiency.
Responsible to report the serious adverse event and adverse event to sponsor with in time period.
Review and summarize miscellaneous reports and documents; prepare background documents and outgoing mails as necessary.
Provide superior customer service to all patients
Responsible for scheduling appointments effectively, and managing conflicts if any
Responsible for creating and updating study subjects electronic health records, source documents, master files.
Managing custody, circulation, control, retention and secure disposal of confidential information.
Arranging / scheduling clinical visits of patient
Comply with all SOPs, regulations, Good Clinical and Ethical Practices.
Screen, recruit and enroll eligible subjects and monitor their status.
Coordinating clinical trial with safety, integrity and efficiency.
Responsible to report the serious adverse event and adverse event to sponsor with in time period.
Review and summarize miscellaneous reports and documents; prepare background documents and outgoing mails as necessary.
Provide superior customer service to all patients
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