The Operating Ceter for INA-RESPOND (OCIR) urgently needed for Site
Assessment Liaison and Preparedness Evaluation
Base: Jakarta
Contract Duration 1 (one year) starting in Mid of January 2012
Interesting candidate please send your CV, Certificates, and application
letter before Jan 17, 2012 to: herman_kosasih@yahoo.com
POSITION TITLE: CLINICAL RESEARCH SITE SPECIALIST
Job Description:
Manage and provide a range of clinical research support activities for the
Indonesia Research partnership on Infectious Disease (INA-RESPOND)
Operation Center in Jakarta, Indonesia. Duties include but are not limited
to: provide clinical research site training and support for protocol
implementation and site development activities; conduct site visits;
conduct quality management activities, manage work with other members of
the operation center to ensure that all protocol related activities are
completed according to client timelines; provide support to the protocol
development team; conduct review of protocol documents; assist with
development of project budgets; serve as data manager. Candidate must be
comfortable working in a fast-paced environment and must be fluent in
Indonesian and English
DUTIES AND RESPONSIBILITIES
Site Liaison
Site Assessment and Preparedness Evaluation
Training: Plan, coordinate and help conduct clinical research site staff
training (e.g. GCP)
Data Management: responsible for CRF
Protocol Development and Implementation
Base: Jakarta
Contract Duration 1 (one year) starting in Mid of January 2012
Interesting candidate please send your CV, Certificates, and application
letter before Jan 17, 2012 to: herman_kosasih@yahoo.com
POSITION TITLE: CLINICAL RESEARCH SITE SPECIALIST
Job Description:
Manage and provide a range of clinical research support activities for the
Indonesia Research partnership on Infectious Disease (INA-RESPOND)
Operation Center in Jakarta, Indonesia. Duties include but are not limited
to: provide clinical research site training and support for protocol
implementation and site development activities; conduct site visits;
conduct quality management activities, manage work with other members of
the operation center to ensure that all protocol related activities are
completed according to client timelines; provide support to the protocol
development team; conduct review of protocol documents; assist with
development of project budgets; serve as data manager. Candidate must be
comfortable working in a fast-paced environment and must be fluent in
Indonesian and English
DUTIES AND RESPONSIBILITIES
Site Liaison
Site Assessment and Preparedness Evaluation
Training: Plan, coordinate and help conduct clinical research site staff
training (e.g. GCP)
Data Management: responsible for CRF
Protocol Development and Implementation
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